Monday, September 24, 2018

Youtube daily report Sep 24 2018

the heart electrical signals are initiated in its natural pacemaker the

sinoatrial node or SA node and travel through the atria to reach the atrial

ventricular node or AV node the AV node passes the signals on to the bundle of

his which then splits into two branches that conduct the impulses to the two

ventricles the SA node is composed of two major cell types p, for pacemaker cells

generate electrical impulses and t, for transitional cells transmit these

signals to the right atrium and subsequently to the rest of the cardiac

conduction system sinus node dysfunction occurs when any of these cells cease to

function properly failure to produce electrical impulses by P cells leads to

sinus pause or sinus arrest while delay or failure of signal transmission by T

cells results in SA exit blocks on an ECG sinus pause or arrest can be seen as

a brief absence of P waves which can last for seconds to minutes in most

cases a downstream pacemaker in the atria, atrioventricular junction or

ventricles will take over the pacing function producing so-called escape

Beats or rhythms and thus preserving heart rate and function until the SA

node recovers and fires again but long pauses may cause dizziness fainting and

possibly cardiac arrest in SA exit blocks the SA node discharges normally

but the impulses are slow to reach the atrium or completely interrupted before

reaching the atrium there are three degrees of SA blocks similar to the

three degrees observed with AV blocks in first degree SA block there is an

abnormal delay between the firing of the SA node and transmission to the atrium

because SA node firing is not significant enough to be seen on a

standard 12-lead ECG this type of block cannot be detected on a surface ECG in

second-degree SA block type one the electrical signals are delayed

further and further with each heartbeat until a p-wave is missing altogether due

to the diminution in the increment of the delay the PP intervals are

progressively shortened before the dropped P wave this pattern results in

pauses and the appearance of grouped beats the duration of each pause is less

than 2 PP cycles in second-degree sa block type II some of the electrical

signals do not reach the atrium on an ECG this is seen as intermittent dropped

P waves the pauses are multiple usually twice of the PP interval third-degree sa

block is a complete block P waves are absent this type of sa exit block is

indistinguishable from a sinus arrest sinus node dysfunction is most commonly

due to degeneration or scarring of the SA node tissue which can result from

aging other heart diseases or diabetes other causes may include certain

medications or an excessive vagal tone

For more infomation >> Sinus Node Dysfunction, Animation - Duration: 4:01.

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Pumpkin Pie Overnight Oats (Vegan) - Duration: 1:52.

For more infomation >> Pumpkin Pie Overnight Oats (Vegan) - Duration: 1:52.

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An unlikely triathlete pens a

For more infomation >> An unlikely triathlete pens a

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Opel Corsa 1.3 CDTI ECOFLEX S/S COSMO - Duration: 1:08.

For more infomation >> Opel Corsa 1.3 CDTI ECOFLEX S/S COSMO - Duration: 1:08.

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Fiat 500X S-Design - Duration: 1:09.

For more infomation >> Fiat 500X S-Design - Duration: 1:09.

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Hip-Hop's Love For 'SpongeBob Squarepants' | Genius News - Duration: 3:36.

TIA: On April 30,1999 the first episode of 'SpongeBob Squarepants' aired on Nickelodeon.

And with the beginning of the show also came the beginning of SpongeBob's rap career.

PATRICK: Who's ready?

SPONGEBOB: I'm ready!

PATRICK: Who's ready?

SPONGEBOB: I'm ready!

PATRICK: Who's ready?

SPONGEBOB: I'M READY!

TIA: According to Genius data, the cast of 'SpongeBob' have made hundreds of appearances

in hip-hop lyrics since the series premiere.

TIA: So, we decided to revisit a few of our favorites.

SPONGEBOB: Quick Patrick without thinking, if you could have anything in the world right now,

what would it be?"

PATRICK: Uh, more time for thinking!

TIA: The main character in the show is SpongeBob Squarepants, the energetic fry-cook and jellyfishing

enthusiast.

TIA: The earliest hip-hop reference to SpongeBob was in 2004 on D12's "Keep Talkin'."

TIA: Since then, SpongeBob alone has been referenced over 100 times,

in songs ranging from Smokepurpp to Wu-Tang.

TIA: Producer Izak even sampled SpongeBob's voice directly as his producer tag, most famously

in YBN Nahmir's "Rubbin Off The Paint."

YBN NAHMIR: That's what I thought you said, now let me offer this as a rebuttal.

SPONGEBOB: That's what I thought you said, now let me offer this as a rebuttal.

IZAK: Like, every time I, like, see reaction videos on YouTube people be like, is that SpongeBob?

And then the beat comes and then they'll be like, Oh!

Okay, cool.

TIA: But SpongeBob isn't the only person in Bikini Bottom who's made it in the rap game.

TIA: SpongeBob's best friend Patrick also has a few cameos in hip-hop lyrics.

TIA: SpongeBob's neighbor and coworker Squidward has a number of hip-hop mentions himself,

even though he probably wouldn't be too happy to hear them.

SQUIDWARD: Oh no.

PATRICK: E minor, alright! Yeah!

TIA: Other character references include Mr. Krabs and his daughter, Pearl.

TIA: Sandy Cheeks

TIA: And even Plankton.

PLANKTON: You may win this time.

Shi-a-kazeem!

TIA: In late 2017, the 'SpongeBob Squarepants' Musical premiered on Broadway.

The play featured musical credits from T.I. and was nominated for a Tony Award for

Best Original Score.

TIA: And it's safe to say hip-hop's love for 'SpongeBob' is definitely mutual.

TIA: I'm Tia with Genius News, bringing you the meaning and the knowledge behind the music.

For more infomation >> Hip-Hop's Love For 'SpongeBob Squarepants' | Genius News - Duration: 3:36.

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Audi A4 € 2.607,- DEMO voordeel 1.4 TFSI Sport S-line edition S tronic 150 pk - Duration: 1:07.

For more infomation >> Audi A4 € 2.607,- DEMO voordeel 1.4 TFSI Sport S-line edition S tronic 150 pk - Duration: 1:07.

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Protein Structure and Folding - Duration: 7:46.

We all have things that challenge us- and for me- it is folding.

Sheets, towels, shirts- let's just say I invest in a lot of anti-wrinkle laundry spray.

Amazing invention.

My issue with folding extends to paper too.

I know foldables in the classroom can be a powerful way to organize concepts, but for

me, it was the actual folding part that I tended to get stuck on.

You may think of folding as a convenience- of a way to take something and make it more

organized or condensed so it doesn't have to take up as much space.

This is true.

But in biology, folding can also have a lot to do with function.

We've mentioned how amazing proteins are.

They can play so many roles.

They can make up channels, be a part of structure, serve as enzymes for important biological

processes, be involved with protecting the body...just to name a few.

We've also mentioned that you are making proteins, all the time, in a process known

as protein synthesis.

But the conclusion of producing a long chain of amino acids doesn't necessarily equal

a functional protein.

There are modifications to a protein that often need to happen in order for it to be

functional.

By modifications, we can mean many things.

It might be adding certain chemical groups, such as phosphorylation---something to definitely

explore.

But another important event to make a functional protein is---believe it or not---folding.

But before we get into protein folding, let's talk about shape and why shape is so important.

Shape and function, in biology, frequently go hand in hand.

In our cell signaling video, we mention how protein receptors and the signal molecules

that bind them can fit together so perfectly to start some type of cellular response.

Or in our enzyme video, we talk about how enzymes---which are frequently proteins---have

a very specific shape for the substrates that they build up or break down.

When we talk about the way proteins are folded, we need to understand the different levels

of protein structure because there are different ways of folding that can happen in the different

structural levels.

The first level of protein structure is primary structure.

This is the sequence of amino acids that make up a protein.

Amino acids are the monomer---which means the building block---of a protein.

They are held together by peptide bonds.

In protein synthesis, amino acids are added to form a polypeptide chain and proteins are

made of 1 or more of these polypeptide chains.

Genes, which are made of DNA, determine the order and number of these amino acids.

That sequence is critical to the protein's structure and function.

In our mutations video, we talk about how one amino acid can be changed in sickle cell

disease.

Even a single change of an amino acid has the potential to affect a protein's function.

We do want to point out- each amino acid has a carboxyl group, an amino group, and a R

group- an R group is also called a side chain.

So even though we have them drawn here like a chain of circles, realize that each of those

circles we're drawing is an amino acid like this.

Next, we move on to secondary structure.

Folding is really going to start to happen.

In secondary structure, the sequence of amino acids that we mentioned in primary structure,

can fold in different ways.

The most common ways are the alpha helix and the beta pleated sheet and which one of these

foldings the protein does depends on the amino acid arrangement it has.

Both of these shapes are due largely in part to hydrogen bonds.

Those hydrogen bonds can occur at specific areas of the protein's amino acids.

Specifically, these are hydrogen bonds involving the backbone of the amino acid structure-

we're not focusing on the R groups right now.

On to tertiary structure.

This is looking at more folding that occurs in the 3D shape of a functional protein.

And a lot of this is due to something we haven't mentioned much…the R groups.

Also called side chains.

See, the amino group and the carboxyl group are generally standard parts of an amino acid,

although the R group found in amino acids can vary among different amino acids.

That means, the R group can define the amino acid and can make amino acid behave a certain

way.

For example, some R groups are hydrophilic.

They like water.

Some R groups are hydrophobic.

They don't.

And remember that proteins contain many amino acids which can contain different R groups

and so different areas of the protein can therefore be impacted based on those R groups.

When protein folding is going on, amino acids with hydrophilic R groups may hang out on

the outside while hydrophobic R groups.

Where are they?

They may hang out in the inside part of the protein.

The 3D shape is due to other interactions besides hydrophobic interactions.

Ionic bonds, Van der Waals interactions, disulfide bonds, and hydrogen bonds- all involving the

R groups- also influence the folding occurring in tertiary structure.

Something to explore.

Now when we've been talking about a protein, we've been talking about a polypeptide chain

that has been folded into a functional protein.

But proteins can be made of 1 or more polypeptide chains and in quaternary structure---you are

looking at a protein consisting of more than 1 polypetide chain.

Each of these polypeptide chains can be a subunit and interactions between them such

as hydrogen bonds or disulfide bonds can keep them together.

Going back to the folding, I know what you might be thinking.

Who is doing this folding anyway?

Are the proteins just folding themselves?

Well, the interactions mentioned like hydrogen bonds and R group interactions are occurring

depending on the protein's own amino acids.

One reason why amino acid sequences are very important for protein function.

But folding is far more complex than that, and there can be intermediate steps involved

when a protein is folding.

In fact, there's a phrase you can search called the protein-folding problem to learn

more about the questions scientists continue to explore regarding protein folding.

Research has shown that proteins often have help in the folding process.

Chaperonins, for example, are proteins that can help with the folding process.

They have almost a barrel shape.

Proteins go into them, and the chaperonin tends to have an environment that is ideal

for the proteins' folding.

This can help the protein to be folded correctly so it's functional.

Just wish I had something like that for my towels.

All of these interactions we mentioned in primary, secondary, tertiary, and quaternary

structure are paramount for a mature protein to have its correct shape so it can carry

out its function.

And that's very relevant!

There are many diseases that are related to protein misfoldings.

Check out some of our further reading suggestions in the description about that.

One last thing we haven't mentioned: each protein has an ideal environment for functioning

which might include a certain temperature or pH range.

If the protein is exposed to something outside of its ideal temperature or pH range- exposed

to high heat for example- you can disrupt the interactions that we have talked about

taking place at the different structural levels.

This can denature the protein, which disrupts its shape.

This prevents it from functioning correctly.

And depending on what caused it to be denatured, sometimes you are interfering with many levels

of protein structure.

Sometimes, it's just one or two levels.

Sometimes denaturing a protein may be reversible.

But in many other cases…it's not.

The environment that a protein is in definitely matters for its functioning.

Well, that's it for the amoeba sisters, and we remind you to stay curious!

For more infomation >> Protein Structure and Folding - Duration: 7:46.

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Treatment Targets, Target Engagement, And Target Populations in Mental Health Services Research - Duration: 1:30:35.

>> WENDY: Good day, everyone, and welcome to today's webinar titled "Treatment Targets,

Target Engagement, and Target Populations in Mental Health Services Research to Improve

Public Health: Examples from the Field."

At this time, all participants are in a listen-only mode.

If you would like to submit a topic or technical-related question, you may do so at any time via the

Q and A pod located at the bottom of your screen.

Please note, this webinar is being recorded.

I will be standing by if you should need any assistance.

It is now my pleasure to turn the conference over to Makeda Williams.

>> MAKEDA WILLIAMS: Thank you so much for the logistics, Wendy.

Good morning, good afternoon.

My name is Dr. Makeda Williams.

I'm from the National Institute of Mental Health Office for Research on Disparities

and Global Mental Health.

I'm pleased to welcome you to today's webinar titled "Treatment Targets, Target Engagement,

and Target Populations in Mental Health Services Research to Improve Public Health: Examples

from the Field."

This is the second in a series of four webinars in our 2017 webinar series focused on global

mental health issues.

Please note that this webinar is being recorded, and it will be posted on our website.

It now gives me great pleasure to introduce to you the speakers for today.

Their biosketches are located on the webinar website, but I just want to give you a brief

overview for each of the speakers.

Dr. Mary McKay is the Neidorff Family and Centene Corporation Dean of the Brown School

at the Washington University in St. Louis, St. Louis, Missouri.

She has significant experience in child mental health services and implementation research

methods as well as 20 years of experience conducting HIV prevention and care-oriented

studies.

Dr. McKay is a principal investigator for one of NIMH's research partnerships for scaling

up mental health interventions in low- and middle-income countries, titled "Strengthening

Mental Health and Research Training in Africa," otherwise known as SMART Africa.

SMART Africa is a transdisciplinary collaborative partnership to engage stakeholders from academia,

government, nongovernmental organizations, and local communities in Uganda, Kenya, Ghana,

and South Africa in addressing child mental health burden, evidence-based intervention

implementation, scale-up, and service gaps.

Prior to joining the Brown School, she was the McSilver Professor of Social Work and

the Inaugural Director of the McSilver Institute for Poverty Policy and Research at New York

University's Silver School of Social Work.

Our next speaker is Dr. Mary Acri.

She is a senior research scientist at the McSilver Institute for Policy Poverty and

Research, and research assistant professor at New York University School of Medicine's

Department of Child and Adolescent Psychiatry.

She is also faculty within the Center for Implementation and Dissemination Science in

States for Children and is an adjunct faculty member at the Silver School of Social Work

at The New York University.

With a background in clinical social work, Dr. Acri's research interests center on developing

and testing interventions to enhance the detection and treatment of mental health problems among

children and their caregivers.

Our next speaker is Dr. Ozge Sensoy Bahar, and she is a research assistant professor

at the Brown School, Washington University in St. Louis, St. Louis, Missouri, with research

interests in child and family well-being in global contexts characterized by poverty and

associated stressors.

Her current research program focuses on youth experiences of child work and labor, as well

as the individual, family, and contextual factors leading to child labor in two country

contexts.

Those would be Turkey and Ghana.

The goal of her work is to develop culturally and contextually relevant interventions to

reduce risk factors associated with child labor.

Dr. Sensoy Bahar serves as a lead to the SMART Africa Center.

Our next speaker is Dr. Denise Pintello, currently serving as Chief of the Child and Adolescent

Services Research Program and also as Acting Chief of the Dissemination and Implementation

Research Program at the NIMH.

Before joining NIMH she served as a special assistant to the Director and the Deputy Director

of the National Institute on Drug Abuse, otherwise known as NIDA, for 11 years, and she oversaw

the implementation of innovative scientific initiatives and special research dissemination

projects.

As a social worker for more than two decades, Dr. Pintello worked extensively in child welfare,

mental health, and substance abuse and provided clinical, case management, and supervisory

services for over 1,500 children and adults.

She has also conducted research studies within the fields of child welfare, domestic violence,

juvenile justice, mental health, and substance abuse.

Last but not least is our final speaker, Dr. Michael Freed.

He is the NIMH Service Research and Clinical Epidemiology Branch Chief.

Under his guidance, the branch helps set Institute research priorities, develop funding initiatives,

and administer a public health�oriented research portfolio to increase access, continuity,

quality, equity, efficiency, and value of mental health services to those in need.

The branch also manages the dissemination and implementation research portfolio for

the Institute.

Dr. Freed joined NIMH from the Department of Defense where, as the research director

of an interdisciplinary team of researchers, clinicians, and support staff, he worked to

transform behavioral health care across the military health system.

He served in principal and co-investigator roles on several key epidemiological and health

services research studies, as well as clinical trials.

I'm delighted to welcome all of our speakers today to talk to us about mental health services

research, and I will now turn it over to Dr. Michael Freed.

>> MICHAEL FREED: Perfect.

Thank you, Makeda, for that wonderful introduction.

When we think about the perfect intervention package, we want to make sure that evidence

supports whether and how the intervention is effective or not.

Oftentimes what we hear as program officers from researchers curious about conducting

a clinical trial is, "Hey, I'm using an untested intervention and wondering if it works."

Or, "I want to develop an intervention and ensure that it works in my setting."

The question that is the catalyst for this webinar is really what if it does not work?

Can we look under the hood and really examine why it doesn't work?

On this slide you see, when we talk about the intervention package, what you see is

a present.

A wrapped present.

There are lots of ways to think about whether an intervention works, and we think long and

hard about this.

There are different frameworks, and RE-AIM is one of those frameworks.

For example, we think about intervention Reach, and that's the percentage and representativeness

of the target population included.

We think about Effectiveness, which is does it work?

Does the intervention work on primary outcomes?

We think about Adoption: How representative of setting and intervention staff to what's

really happening in the real world?

We think about Implementation: Is the intervention delivered per protocol?

We also think about Maintenance, which is will the intervention be sustained with fidelity

following completion of the study?

Another way to think about this is something called the PRECIS-2, which is really asking

the question, how pragmatic is the intervention?

How well does the intervention fit into the service setting, whether it works or not?

It really still has to be the right fit for the setting.

We can ask questions about the tradeoff of how pragmatic a trial might be and its generalizability,

and even maybe who judges how pragmatic a trial is.

Finally, when we think about whether an intervention works, we might think about this through an

implementation science lens.

How do we value the importance of effectiveness, like clinical data, when designing the study?

Perhaps there is robust evidence that the intervention improves ... that there's enough

evidence that the intervention improves clinical outcomes, and the research question really

is about which implementation strategy is best, which is how do we best implement the

best practice?

Moving even a step forward, perhaps there's already enough research evidence that we can

move straight to implementation.

In 2014, NIMH developed new requirements for clinical trials.

These requirements essentially codified what good intervention developers were already

doing, and that's really to understand mechanism.

The term that's used is called target, and this is to differ from what we think about

a target population or a target outcome.

Here when we think about a target, it's a factor that an intervention is intended to

modify based on a hypothesis that modification of that factor will result in improvement

of symptoms, behavior, or functional outcomes.

This might be easy to think about in terms of drug development or even psychotherapy

development.

Some examples from drug development might be molecular processes, synaptic- and circuit-level

networks.

For psychotherapies, we might think about cognitive or emotional processes, but this

can be applied for services interventions too.

We might think about provider behavior, decision-making processes, or organizational policies.

But again, these are examples.

I also just wanted to distinguish between moderators and mediators.

This is an important distinction.

Both are very important in any type of research study, but [unintelligible] looking at moderators

are going to be insufficient to meet requirements for clinical trial responsiveness.

We think about a moderator, this is a categorical variable or ordinal variable or continuous

variable that affects the direction and strength of the relationship between an independent

or predictor variable and the dependent or criterion variable.

Juxtaposed to a mediator, which really is sort of the extent that the variable accounts

for the relationship between predictor and criterion.

Put more simply, a moderator is going to answer when will certain effects hold, and a mediator,

how or why do such effects occur?

If we move on to thinking about adaptation of the perfect intervention package, and we

can think about not all interventions and not all treatments will work for everyone,

but it's important to demonstrate a priori, as a rationale, that there's an empirical

rationale for why we're going to make the adaptation.

For example, evidence-based practices exist, and one may erroneously determine that they

don't work for a certain group of people, not because they actually don't work, but

because they were not implemented well.

We really need to understand how much changing the packaging matters, versus changing what's

inside the package.

So if we think about just different presents - so there's some pictures here - we can think

about changing the color of the wrapping, the style of the bow, but really what we want

for any type of adaptation study is an empirical rationale for the specific adaptation or augmentation,

but also, we want empirical rationale for the corresponding mechanism by which the adapted

intervention is expected to substantially enhance outcomes.

This gets a little bit more complicated when we think about advancements in methodology,

and we think about what's happening on the ground in actual service settings.

For example, how do we think about experimental therapeutics when we think about multicomponent

interventions?

Or pragmatic studies where adding research measures is challenging.

The more pragmatic a study is, the less research influence is involved.

Think about multilevel interventions.

Those are interventions that happen at the patient/clinic/health system level, or if

you think about school systems, the child/the classroom/the school.

And we think about non-clinical outcomes.

This is true for dissemination and implementation studies.

We want to think about mental health services clinical trial research beginning with the

application in mind, but really now moving to the grant application.

To make it really easy for us as program staff to be able to evaluate the responsiveness

of the application, we strongly encourage researchers to be very, very clear about identifying

the target or targets, outlining a conceptual framework or empirical basis for the proposed

targets, what's the plan to assess target engagement (and that's measuring the target),

and then describing the analytic strategy involved.

This makes it, again, easy for us as program staff but also for reviewers to look at and

evaluate the quality of what you're proposing.

There are multiple mechanisms, grant mechanisms that accept clinical trials, but here are

some broad frameworks.

For an R34, this is really a pilot study focused on refining and optimizing interventions for

use with broader target populations or for use in community practice settings.

We want feasibility of a study, but that's not sufficient for a responsive application.

Studies should be designed to explicitly address whether the intervention engage the mechanism

that is presumed to underlie the intervention's effects.

When we think about an R01, this is a mechanism that supports trials that are statistically

powered to provide a definitive answer regarding the study's intervention effectiveness in

comparison to usual care practices or some alternative group.

Studies should also be designed to address hypotheses regarding predictors and moderators

of effectiveness and questions regarding mechanisms that underlie clinical benefit.

We also have a collaborative R01 which is used when two or more sites are needed.

We have a variety of funding announcements that accept clinical trials, and some that

do not accept clinical trials.

Here is a website that lists all of them, but we would encourage any researcher or potential

researcher to call us or email us.

The program staff are happy to help direct you to the best-fitting funding announcement

for your research idea.

Please note that all NIMH funding announcements accepting clinical trials, and this includes

mental health services and D&I trials, do require applicants to follow the experimental

therapeutic paradigm.

There's really no way out of this if you're wanting to propose a clinical trial, and know

that the definition of clinical trial is pretty inclusive, so if you're proposing a study,

please read that definition carefully.

We're also very interested in research to identify new targets, to identify new methods

to measure targets, and to develop new analytic approaches to assess target engagement and

causality.

We know we don't have all the answers, and this is an important line of research that

we want to encourage, and our branch in particular is interested in research that aligns to NIMH

Strategic Research Priority number 4 from the NIMH strategic plan.

We're really excited today.

We have some great speakers lined up - Doctors Mary McKay, Mary Acri, and Ozge Sensoy Bahar

- to talk about two really important studies, one domestic and one global.

You can see them here.

These are great examples from the field that we're really excited to showcase.

Then finally Dr. Denny Pintello will lead a discussion at the end and field questions.

Thank you, and we certainly want your research ideas, we want your application, and please

contact us if you have any questions.

With that, turn it over to Dr. Mary McKay.

>> MARY MCKAY: Great.

Thanks so much, Mike and Makeda, for the warm words of welcome.

I'm assuming that I'm coming through okay.

I am incredibly grateful for this opportunity to share two examples of studies that we have

currently in the field.

Myself and my really talented colleagues, Mary and Ozge, we're going to try to focus

in on the design of these studies, the methods that go along, as we try to look at both targets

of our interventions, look at the outcomes of our interventions, and look at potential

factors that influence the adoption, implementation, and sustainability of interventions, all while

trying to go to scale with some of the interventions for kids and families in our mental health

services studies.

I'm going to talk about two studies.

One's set, the first one, in New York City.

This is a hybrid effectiveness implementation study of an intervention, a family strengthening

intervention delivered via groups, family groups, that targets kids with serious behavioral

difficulties.

Mary and I are going to talk through that New York City study, and then Ozge and I are

going to pick up how do we learn from New York to influence what could potentially help

kids and families in Africa?

And I want to emphasize that there's a bidirectionality in our thinking, that we are also very interested

in what we learn from our African scale-up experiences and how that influences urban

centers like New York City.

We're going to talk about both the work first in the U.S. as well as then go global and

take us to Africa around some of the adaptations that are clearly needing to be made, but also

what can we learn from the U.S. in terms of family strengthening?

There is a tremendous set of colleagues that we have, both in the U.S. as well as global

colleagues, that are part of these research teams.

There are also amazing training opportunities for research interests as beginning professionals,

so I just want to express my sincere gratitude to our outstanding staff, as well as our committed

participants and our colleagues that really have helped us to field, I think, probably

the most ambitious study I've ever been involved with in the U.S.

Let me launch into the New York study first and set it up in terms of the issues that

we're trying to address, and then Mary Acri will take over and talk a little bit about

methods and where we are in the field.

First, our particular research group focuses really exclusively on young people and their

families and communities impacted by poverty.

If you think about addressing children's behavioral success, addressing their serious conduct-related

difficulties, you must take into account the complex circumstances of young people and

their families' lives.

There's tremendous trauma exposure.

There's tremendous social ills that kids and families and communities are confronting that

are associated with poverty, and also I think equally important is they are showing coping,

resilience, thriving in the face of fairly significant adversity.

Taking into account both the complexity of young people, families' and communities' lives

as well as their strengths to successfully address child mental health difficulties is

really the perspective that we come from.

Mike talked about targets, and those of us that feel very strongly about testing intervention

packages and services for kids and their families understand greatly that without a real focus

on engagement, retention in both our clinical trials as well as services in general, we're

going to only come away with partial answers to our research questions.

This particular slide has been in my slide deck for a long time, but what's important

to note is that these statistics, there hasn't been nearly as much movement as I would wish,

and I think many of us would wish, around engagement of kids and families that need

services with the service systems that are set up to serve them.

We still, many of our clinical trials are plagued and certainly our service systems

are plagued with the phenomenon called no-shows, early dropouts, and really what those mean

to us, as researchers that are interested in kids and families, is incredible missed

opportunities for kids and families to actually address their needs, particularly early on,

and so I'll come back to that point in just a little bit.

As we think about putting together an application, putting together a service package as Mike

talked about, there are many factors that we need to take into account.

The complex circumstances, the strength and resilience of kids and families as they approach

an intervention like ours, as well as obstacles and complexities that exist at the family

level, at the service system level, at the community level.

This slide just identifies a set of core issues that we often consider as we're putting together

intervention capacities � intervention packages, that these issues must be addressed.

And so service capacity�I'll just highlight that one issue from this particular slide�Part

of why we chose to test a group-delivered intervention had everything to do with the

struggle that our clinic partners have in terms of really having the capacity to see

families, long waiting lists, or capacity to serve kids and families outside of school

hours.

We chose that group-delivered intervention to address some of those issues, and I'll

talk about that in a little bit as well.

I think where we are in the field, and I appreciate either Makeda or Mike saying how many decades

I've been in the field.

It's been a long time.

We have come a long way in terms of creating evidence-based programs, services, that really

can be of substantial assistance to children and their families, can really improve children's

mental health, improve parenting and family supports for children.

And I'm happy to note that this particular intervention that we're testing is on the

National Registry of Evidence-Based [Programs and] Practices [NREPP].

However, despite the unbelievable advancement in our published clinical trials, in our main

psychotherapies, in our medication advances, in our community- and home-based services

that really have strong evidence behind them, we have continually experienced obstacles

to those interventions, those practices being implemented in real-world settings, in public

safety net clinics.

And so that's really where we're spending our time as child mental health scientists.

It's really thinking about how do we close the gap between what we know to potentially

be helpful, and actually how do we understand how to close that gap between really kids

and families getting access to those services, taking advantage of them, and having good

outcomes?

We've explained that gap as real disappointment around our challenges of disseminating these

practices.

Our group has been really, and others have been really trying to take a part.

Where does implementation, where does dissemination, where does closing the gap go wrong?

We think about this as a multilevel problem, that the alignment potentially with young

people and their families, their needs, and what we put together is off.

That there's also been potential mismatch between the perspectives and skills of what

the existing workforce can deliver and are interested in delivering, and how our intervention

packages have been put together.

Then because we work almost exclusively in low-resource settings, whether we're talking

about in the U.S. or globally, to really think about from the very beginning what's the alignment

between the resources, the funders, the payers, the connection with existing policy and procedures,

and what we're proposing?

I think that these have given us some opportunities to adjust the intervention package and to

think about modifying the evidence base to potentially be more successful in terms of

implementation.

Adjusting and correcting for those misalignments, mismatches, really learning from trials like

the two that we're going to put forth for you today, and humbly, what I appreciate about

what Mike said, learning what works, but actually learning from some of our failures is incredibly

important to this ongoing program of research if we're going to improve kids' mental health.

Just some background around what's the particular space that we're working with in terms of

kids and families: We are identifying really one of the primary reasons that kids get referred

to mental health services, and these are oppositional defiant disorders, conduct disorders, these

serious behavioral challenges that kids experience that help them be unsuccessful at home, at

school, and in community.

Prevalence varies widely.

In the poverty-impacted communities and service systems that we work in, prevalence can be

really quite high.

Kids are struggling, and their behavior is calling attention to those struggles that

kids have.

We also know that, from the evidence base, that family collaboration, parenting, supportive

family processes, organized family processes, are critical to kids' behavioral success,

and yet poverty disrupts parenting, disrupts family processes, undermines parents' mental

health.

We're really trying to think in a comprehensive way.

If we want kids to be behaviorally successful, how do we support their families?

How do we address adverse circumstances of families?

Our interventions try to think about issues simultaneously, which is improving children's

behavior, strengthening parenting, understanding the complex situations that families find

themselves in�their stress, their strains that undermine parenting�and then starting

to draw on also evidence-based approaches like parent management training and others

that really can be helpful to parents, but often haven't been tested in extreme poverty

circumstances both here in the U.S. as well as globally.

How do we modify those approaches, bolster those approaches, so they're likely to more

comprehensively meet kids' and families' needs?

We also take a pretty high priority on what are the common barriers that families experience.

They can be internal to families, like stigma and stress and real sensitivity around being

told what to do as a parent, and how do we think about putting those barriers as well

as other real access barriers together so that we actually have engagement interventions

embedded in our service package that we're testing both in New York as well as globally?

In sum, we have put together a study that is now in its third year, that aims to generate

new knowledge, to address some particular areas that we think are in need of new knowledge

in the child mental health services and implementation realm.

We need new knowledge around engagement of low-income families with conduct challenges.

What are some of the intervention packages that can actually, really penetrate the population

of kids and families in need?

We need to really take a look at can we design options for safety net clinics that can involve

families, and then can be evidence-informed?

We need to look at not just small tests of effectiveness, but also tests of scalability,

particularly in resource-constrained settings, and we're hoping by these types of studies

to open up a menu of options for policymakers to support the uptake and the integration

of service innovations that have evidence, but that have been used in public systems

so are much more likely to be scalable across state systems, or country systems in the case

of our global work.

What is our intervention package that we are testing and trying to then understand what

works about that package or not?

That's the effectiveness part of our study.

Then what can we learn about, as Mike talked about, the targets within that intervention,

the mediators, as well as some contextual targets that I'll talk about that make implementation

and scalability, sustainability more possible?

Our intervention package is a multiple family group [MFG].

This is a group of families that come together.

The sessions that families work on are guided by a protocol, all meant to strengthen parts

of family life and parenting that have been empirically linked to kids' conduct-related

difficulties, serious conduct-related difficulties, and their behavioral success.

Remember, I talked about service capacity.

These groups are relatively large.

Up to eight families meet together, both children as well as their adult caregivers, and this

multiple family group and the protocol that guides these group sessions are laser focused

on family factors, that when strengthened have been implicated in the onset and maintenance

of childhood DBD [disruptive behavior disorder].

What does that mean?

There's a set of factors within families, parenting, that when weakened really have

been strongly linked to kids' conduct difficulties.

The hypothesis around this work is that if strengthened, kids' behavioral difficulties

should actually improve pretty dramatically.

Our materials are available through NREPP, and we've completed one randomized controlled

trial and effectiveness study in a relatively small number of public clinics that allowed

us to put this forward as an evidence-based practice [EBP].

Mary will talk about we are no longer in a small number of clinics, but now across a

New York City service system, attempting to both test the effectiveness, take a look at

family- and clinic-level targets that lead to both effectiveness as well as implementation

and scalability of this particular study.

What are our targets for the multiple family group?

What are the family influences that we work on to strengthen within families so that kids

can be behaviorally successful?

This is a table that was created with strong collaboration with parent consumers as well

as our provider partners.

This is actually, what we like to think about, is the evidence base of what families can

do to help their kids who are struggling behaviorally, but in four words that begin with R and two

words that begin with S. Why did we break down these components of our intervention

in this way?

Well, because we wanted the evidence base to be transparent to our parent consumers,

our parent participants in our study, as well as our providers.

We needed to break down that evidence so that you could actually remember what you were

working on session to session, week to week with families, and the empirical rationale

for why we were working on those things.

Rules is the umbrella term for family organization, consistent parenting.

Responsibility relates to parents really providing leadership within a family, children contributing

to the mission of the family.

Relationships relates to family warmth within family support.

Respectful communication, talking and listening across caregivers and children.

Those four Rs come out of the parent management training literature and have been strongly

linked to kids' behavioral success.

What was less clear in the parent management literature, but clearer to us as you take

apart the clinical trials, the evidence-based programs, is that without also additional

focus on stress and social support, which are highly related to engagement in services

and engagement in trials, as well as your ability to change what you're doing as a parent

in a family�without also adding those two Ss, the evidence base really was less relevant

and potentially less effective with the populations of kids and families that we were working

with.

In terms of our aims, our particular R01 that is in the field right now is meant to examine

the short-term and longitudinal impact of a multiple family group intervention on young

people who are struggling behaviorally�oppositional defiant disorder, conduct disorder�that

they meet those criteria, although many of our kids are comorbid with many other mental

health challenges.

We see that as a replication of our first completed randomized trial of MFGs.

We also have proposed to look at a specific set of family-level mediators at the parents

and family level, and what is the impact of changing those mediators, those four Rs and

two Ss, on child outcome?

We also think that clinic and provider-level factors will influence whether we are able

to implement this intervention and sustain it within particular child mental health practices.

We're looking at factors such as readiness to adopt an innovation, motivation.

We're very interested in whether particular clinics and providers can maintain fidelity,

and if they can't, what are some of the explanations for the challenges with that?

That would have been enough, the first three points, but this is a Type 2 effectiveness

implementation study, and so we also propose to test an implementation strategy.

We're calling them CITs, clinic implementation teams.

We think that with extra support at the clinic level, that we can support providers to overcome

some of the barriers that they might experience to up the implementation and integration of

a multiple family group within their particular clinic setting.

This is how we think about the first set of four Rs and two Ss, that our multiple family

groups specifically target those influences, and that those should relate to children's

outcomes.

Then again, this is just the picture of how we think about clinic and provider-level moderators

and their influence on whether we're able to impact the family-level variables, family-level

targets, that we're trying to influence, and whether if we intervene with a CIT, a clinic

implementation team, and some extra on-the-ground support, that there is a difference in those

moderators and how that impacts family success and then ultimately child outcomes.

What are clinic implementation teams?

They've been developed from prior work.

They come out of quality improvement work within New York State.

Then those clinic implementation teams are working with a subset of our providers and

directors.

They're kind of internal champions, and they develop site-specific plans to address any

obstacles that come up with MFG implementation, fidelity, and there's lots of complementary

work that we drew on from Charles Glisson and others.

I'm going to go through one more slide, Mary Acri, around some of our design choices, and

then I'll transition over to you.

We really thought long and hard around what were some of our design options, and chose

a clinical effectiveness part of our study that examines the intervention impact.

We think about that as replication of our first R01.

We drew into our design methods that examine mechanisms of change and variables that moderate

outcomes, and we also drew on implementation trial methods to examine strategies that potentially

help integrate and support fidelity within our particular clinics.

We chose a Type 2, as I said, hybrid effectiveness�implementation research design, which connects both effectiveness

and implementation, and we really do appreciate the support of our program officials, our

national colleagues, as we vetted this type of design within our grant application.

We also worked really closely with our parents, consumer collaborators, provider collaborators,

directors, to think through these types of designs, why they potentially would yield

us new knowledge, and were we interested in the answers to these questions in our collaborative

working groups?

Mary, I'm going to turn this over to you to talk through the pretty ambitious set of methods

that we both proposed, but now are in the middle of actually implementing this trial,

and then I'll pick it up as you take us through so that we can leave New York City and go

on to the globe.

Mary Acri?

>> MARY ACRI: Great, thank you.

To talk a little bit about the method: From the New York State Office of Mental Health

we received a master list of all licensed child behavioral health clinics that are located

in the five New York City boroughs.

They were randomized to either the two active intervention arms, which was the multiple

family group alone or combined with a clinic implementation team condition versus services

as usual.

Again, as Mary McKay had said earlier, MFG is a 16-week group.

They meet weekly, and there's at least two generations per family, so that can include

caregivers, grandparents, siblings, the child.

Optimally, this model is administered by a parent peer and a mental health clinician,

and the way we're defining a parent peer is a caregiver who has had the lived experience

of caring for a child with a mental health problem and has successfully navigated the

mental health service system on behalf of that child and family.

The other condition, active condition, is MFG plus a clinic implementation team, and

typically the CITs are comprised of one mental health provider, a supervisor, and a parent

partner.

What they do is convene and provide site-specific support around the changing aspects of the

process, content, and structure of the MFG model while retaining the core elements of

fidelity.

And then the last condition is services as usual, and those are services that that family

and child would receive normally through accessing the service system.

Our randomization procedure was that we were at the clinic level, and we randomized the

condition by borough.

We have a total sample of almost 3,000 caregiver�child dyads and providers, so of that, exactly 2,688

adult caregivers of a child between 7 and 11 years of age who meets criteria for oppositional

defiant disorder or conduct disorder, and then two service providers per clinic.

That comes to something like 45 clinics per condition, 20 caregiver child dyads per clinic,

and then the two service providers per clinic.

Our inclusion and exclusion criteria for caregivers was that they needed to be at least 18 years

of age or older - we are offering this intervention in Spanish and English - and that they must

be the primary caregiver of a child between 7 and 11 years of age who meet criteria for

a DBD, disruptive behavior disorder.

We are collecting a variety of information from the child, family, caregiver, and then

the organizational processes.

The child measures - we're really targeting symptomatology and functioning, and the caregiver

is the main respondent for that information.

We're also collecting information on caregiver and family processes.

In the literature, there's extensive evidence that depression and stress on behalf of the

caregiver is associated with uptake of the parenting principles that these parent management

training programs offer, as well as there is a bidirectional relationship between parental

and child mental health.

We're taking a close look at the caregiver's depression and stress over time.

We are focusing specifically on parenting practices, including family communication,

roles, responsibilities - so, those targets that Mary mentioned earlier - as well as family

support.

We're looking at the perceived relevance of treatment and those processes that have emerged

in the literature as being critical for engagement and ongoing use of services as well as outcomes.

Finally, we're looking at provider measures.

We're looking at how the providers view evidence-based practices, and their perception and beliefs

about participating in family-centered care, and their exposure to different training and

supervisory experiences and how that shapes the practice that they engage in.

This study is guided by several hypotheses.

The first hypothesis is that children who participate in MFG are going to evidence significantly

reduced conduct difficulties and increased functioning over time compared to services

as usual.

Again, as Mary mentioned, that's in service of the replication study from the prior R01.

But we are also interested in looking at the MFG-plus-clinic-implementation-team condition,

and that we believe that children in that condition will evidence the greatest magnitude

of change in outcomes, so that's both behavior symptomatology and functioning over time.

We're also looking again at those four Rs and two Ss and looking for the differential

weight or effect of those variables on outcomes.

Our hypothesis is that stress, relationships, and rules - those will evidence significantly

greater impact on child outcomes over time relative to the remaining Rs and Ss - support,

responsibilities, and respectful communication.

Hypotheses under Aim 3 are looking at those organizational factors that are proposed to

impact sustained use of evidence-based practices in clinic settings.

We're looking at leadership support, and our hypothesis there is that if the leadership

is in support of this innovation being delivered in their clinic, we're going to get significantly

greater impact on implementation and integration in comparison to other factors such as general

readiness to adopt an EBP and the clinic climate, and also that provider motivation is going

to be a powerful variable in terms of impacting MFG implementation and integration, and more

so than other provider-level variables.

Finally, the hypothesis under Aim 4 is that we really are looking at those organizational

factors that will, we think, have a greater impact on implementing MFG.

We're looking at specifically the MFG-plus-clinic-implementation-team condition.

We believe that those folks that are in that condition will evidence significantly higher

readiness for innovation and support, as well as preparedness and motivation to implement

the multiple family group model compared to MFG alone, and that this will be maintained

over time.

We also believe that providers assigned to this condition will evidence significantly

enhanced implementation, so fidelity to MFG, and that they will have started and completed

more groups than the MFG condition alone.

In addition to the quantitative data, we really are interested in looking at barriers and

facilitators to uptake and sustain use of evidence-based practices such as MFG, so we

are going to be conducting qualitative interviews with the clinic implementation teams as well

as additional providers in the clinic.

We have interview guides that are going to consist of semistructured questions relating

to their experience implementing and integrating MFG, including barriers and facilitators that

they encountered through this process.

Preliminarily, again, we are in the beginning of year 3 in terms of our rollout of this

project.

We started engaging the clinics in the services-as-usual condition.

We have currently 41 clinics who are enrolled in that condition, and then we rolled out

MFG and MFG-plus-the-clinic-implementation condition simultaneously.

We at this point have 18 clinics participating in the MFG condition and 5 that are enrolled

in the MFG-plus=-CIT condition, and that number is likely higher because we're changing every

day.

In terms of our preliminary results, we are seeing that the average child is approximately

8 years of age, predominantly male, and of color.

And we have found that the majority of folks that we are approaching do meet criteria for

ODD or CD based upon the DBD rating scale.

Their caregivers tend to be in their late 30s and primarily the mother, biological mother,

and we're finding that although their depression scores are not as high as we anticipated,

they are experiencing considerable stress, and that their family income constitutes them

for being impacted by poverty and living in poverty-impacted communities.

As we move forward with this, we are hopeful that we're going to gain more information

about the children and families that are being served in the public mental health system,

as well as the impact of MFG and this innovative clinic implementation team upon child outcomes,

uptake, and sustained utilization.

>> MARY MCKAY: Mary, thank you so much.

It's Mary McKay again.

I just want to underline a couple things that you said, and then take us to a discussion

about how you can build on a study like the ambitious one that you just described into

other work that will help improve the lives of kids and their families in low-resource

settings.

The first is that this is an overview of our study.

Mary put forward the select measures, the mixed methods that we're trying to employ,

so that we are both using qualitative as well as quantitative methods to come away with

a fuller picture of where we're succeeding and where we're failing.

Also, as we ramp up to enter a full system, penetration of roughly ... Mary's right, things

change pretty quickly.

Even as we put the slides together a month or so ago, as we start to approach penetration

rates of clinics 60% of a system, 70% of a system, we're learning a lot around what are

the directors, what are the influencers of even deciding to enter our trial, picking

up this intervention innovation?

What are their concerns?

I think that we're trying to both concentrate on where are the factors that really facilitate

this work, but also getting deep description of places where there's barriers and failures.

I really give Mary and the entire New York team of staff that really are working very

hard across the system, as well as our New York City system partners, because this type

of study in an entire child behavioral health system would not be possible without tremendous

buy-in at all levels for policymakers, funders, payers, and so we're incredibly grateful.

Just in case, as I go into our work in Africa, you think that this is a study about transporting

what we've learned in the U.S., or particularly in New York, into Africa, I need to tell you

a much more complicated story.

Part of the 20 years that Makeda and Mike referred to into my career, half of my research

portfolio has been focused in children's mental health services research, and most of that

mental health services research was primarily set in the U.S.

But the other half constantly of the portfolio was around kids' mental health and HIV prevention

and care research, not only set in the U.S., but also set first in South Africa and then

in several other countries across the continent.

Part of the prevention work in HIV prevention and the mental health support work that we

were involved in, those interventions were also delivered by multiple family group.

Part of why we brought them back to the U.S. was how well they were received in other global

contexts around kids and their caregivers coming together.

So when we had this opportunity to put together a center that was focused both on child behavioral

health scale-up science, but also building capacity in countries where there were not

necessarily resources for kids, we went to that multiple family group protocol that had

been used in Africa, that had been used in the U.S., that had data behind it across cultural

contexts.

We knew the delivery looked different.

We knew that some of the content was quite a bit different, it was tailored to the context,

but we also knew that it was an acceptable intervention delivery format.

That's a long way of saying that I think about this work as bidirectional, that the global

work learned from the U.S., and the U.S. work definitely leans on what we've learned in

global context.

With that I'm going to introduce very briefly our center that is just a little bit over

a year old.

We call it SMART Africa, Strengthening Mental Health and Research Training Africa Center.

Again, we are focused on the common sets of challenges that children exhibit, conduct-related

problems, disruptive behavior disorders, that can vary in terms of prevalence but put kids

on a serious path for unsuccess at school, at home, in community, and really associated

with quite adverse outcomes without intervention.

So as we took the opportunity to think about what could a center do to support effective

and scalable solutions, we focused on a set, a subset here in African country context,

where we had very strong in-country investigators.

We also knew that some of the issues that we confronted in the public safety net in

New York were highly prevalent in the country context that we were working in in Africa.

Poverty, stress, those were issues in the New York City context, in the U.S. context,

but clearly in what felt sometimes like insurmountable obstacles in our country context in Africa

- the stress and the poverty.

We had to think very seriously about how potentially any evidence-based approach could take into

account the complexity of kids' and families' lives, and we also knew that the evidence

base had not grown up in Africa, in our country partners in Ghana, Uganda, Kenya, and South

Africa.

We had to think very humbly about what we could use from the four Rs and two Ss, from

the multiple family group protocol from the U.S. in SMART Africa.

Here's our specific aims.

The first was to create a platform, a research consortium, that brought together key stakeholders

- very much the same way as we do in our U.S.-based study - that brought together scientists but

also policymakers, the service sector in the NGO space, community and cultural stakeholders,

and really to knit together a group of very, very child-mental-health-interested, family-mental-health-interested

stakeholders in Uganda, Ghana, Kenya, and South Africa, to focus on really thinking

about child mental health burden in those country contexts, evidence-based implementations,

scale-up, addressing the very serious service gaps that exist between those country contexts.

Our second goal in this particular center is to build child mental health implementation

research capacity, and our two capacity-building countries and investigators and collaborators

in those countries are Ghana and Kenya.

We also proposed a scale-up, an EBP scale-up study in Uganda that we will - just similar

to what Mary Acri just laid out, really engage in a scale-up study that tries to understand

what are the multilevel influences on uptake, implementation, and effectiveness, on sustainability

of an EBP, and then to really try hard to then disseminate this information to our policy

and government collaborators.

We had the real privilege of having our National Institute of Mental Health colleagues, including

Makeda, visit most recently our Uganda site, and one of the visits that we made was a very

unnatural visit for many of us who consider ourselves academic.

We went to Parliament to talk about the implications of the work in SMART Africa and how we can

partner with them to inform child mental health policy and funding across the country.

The same way that our New York State and New York City partners are close colleagues to

ours in the New York City study, that's the partnership that we're trying to form in SMART

Africa right from the get go.

How do we achieve these aims, particularly around our network?

We engaged in a recent conference where we've invested hard into what's our theory of change?

What are the goals that we have around children's mental health, both symptoms and functioning?

What are the factors that facilitate and impede implementation to consider multilevel obstacles

as well as facilitators in each one of the country contexts that we're working with?

We're also conducting lots of formative work in country.

A systematic scan of capacities, needs, existing infrastructure, so that we can actually understand

the landscape the same way we do in the U.S.

What are the places that we can actually stand upon, and where are the places we're going

to run into trouble?

Step Three is in capacity-building countries: In Ghana and Kenya, they will conduct small,

randomized effectiveness implementation trials, and in Uganda a large-scale hybrid effectiveness

implementation study will be conducted around our EBP, which is an adapted version of the

multiple family group intervention that Mary and I just described.

Continuously we are trying to learn from every step of this process to inform other scale-up

studies in low-resource contexts, both in the U.S. as well as globally.

This is kind of our map of what our SMART Africa Center is trying to do.

We are trying to network and information share, we're trying to provide technical support,

capacity-building activities, but what I'm going to talk about mostly is our scale-up

research study, and then Ozge will talk about capacity building in other country contexts.

If I didn't say this before, I should have.

These studies take a complete village to really field, and so the collaborative methods that

bring people together across sectors, across perspectives, across stakeholder groups, are

very important and underpin both the work that we do in New York State and New York

City as well as the work that we do globally.

As we have already described, we took this evidence-based practice and the method of

delivery, multiple family groups, that had been used previously in Africa, and designed

a study very similar to what you just saw Mary present.

This is a longitudinal, experimental, mixed-method effectiveness implementation research design.

In group one, in condition one, schools are randomized in this particular design so that

our multiple family groups are going to be delivered by trained parent peers, exclusively

parent peers that are trained and supported, and we're drawing those facilitators from

local planning councils.

Why is that important?

Because trained professional child mental health providers do not exist in the settings

that we work with in any type of scale that could field actual services for kids and families.

In condition two, a set of school multiple family groups are going to be delivered by

trained and supervised community health workers drawn from local primary care clinics.

And finally, we are knitting together comparison mental health wellness and educational supports

within schools so that every kid, every family in need has access to some type of support

in incredibly low-resource settings.

Here's where we work.

What's an incredibly both important opportunity for a country like Uganda, as well as a huge

challenge, is in Uganda kids make up almost 60% of the total population of the country,

and yet kids are incredibly burdened within a Ugandan context by poverty, violence, and

a host of other burdens, which really does potentially compromise the future generation

and the future of a country context without really seriously meeting the mental health

and health needs and security needs of kids within the country context.

We have put together an unbelievable team in Uganda that has done the formative work

that we also did in New York City and New York State about how you think about taking

an evidence-based practice but aligning it to the resources available, the system availability,

as well as the cultural context.

There is lots of work that is done in large and small groups that teachers and caregivers

and clinic directors really dig in deep to both the four Rs and two Ss of intervention

protocol, as well as some other prevention programs that have existed within the local

community context, to really fuse together the evidence base that exists around how do

you help kids with conduct difficulties, but the delivery and the format and the content

really be aligned with community and cultural values and preferences.

This is an example of taking the four Rs and two Ss, but deeply translating those activities

into an evidence-based approach that families would recognize.

(This is actually in English, but also the intervention materials are all translated

into Luganda and I just don't have those language capacities.)

One of the things that I've learned in working in both Africa and the U.S. is they are very

different contexts with very different preferences and resources and norms.

On the other hand, there are some universals.

Parents really care about their kids and their outcomes.

Stress is a really important factor.

Communication within families is really important, and so you'll see some of the same topics

that were not rejected by our collaborative working group�as a matter of fact, embraced,

but then modified in terms of how you discuss those issues within an African context.

I'm going to stop here and turn this over to Ozge, who's going to talk a little bit

about just it's not only an adaptation process and then a scale-up study that will happen

in Uganda, but there's lots of work occurring simultaneously in our other country contexts

around building capacity to do this work, as well as testing and intervention.

Ozge, can I turn that over to you?

>> OZGE SENSOY BAHAR: Thank you, Mary.

As Dr. McKay mentioned, we have two sites, Ghana and Kenya, that are getting ready to

launch their small-scale study using lessons learned from Uganda.

Our Ghana research team is composed of two researchers from the School of Public Health,

two researchers from the Department of Social Work, as well as BasicNeeds as their implementation

partner.

This team has engaged extensively in formative work to get ready for their pilot study.

They had their first stakeholders' meeting in March, bringing together researchers and

practitioners and policymakers.

They have had an onsite follow-up meeting with implementation partner BasicNeeds Ghana

in Tamale to further discuss the details of the partnership.

The research team has completed the review of the adapted manual in Uganda and made some

initial edits in the process of adapting it to the Ghana context, and they have scheduled

visits with BasicNeeds Ghana and community stakeholders in Tamale for initial feedback

on the intervention manual and delivery.

Our colleagues in Kenya, which is our second capacity-building site - our research team

there is composed of three researchers from the Department of Psychiatry at University

of Nairobi.

They are also very busy getting ready for their pilot study.

They had their first stakeholders' meeting also in March, and engaged extensively in

the discussion of the existing mental health policy in the country and the lack of policies

specific to children and adolescents around mental health.

Since then they have continued to engage policymakers.

As a matter of fact, the director of the Mental Health Department within the Ministry of Health

in Kenya attended our conference in early August in Uganda and participated in a panel

that focused on strengthening the dialogue between policymakers and researchers.

The team is currently engaged in forming a working group and working closely with the

Ministry of Health to sketch a mental health policy for children and adolescents that can

be incorporated in the existing mental health policy in the country.

The capacity building is a very critical component of our SMART Africa Center, and our capacity-building

efforts also include the Global Child Health Fellowship that aims at supporting the upcoming

generation of scholars interested in global child and adolescent behavioral health.

We currently have nine fellows, including myself, who come from five different countries,

four of them in Sub-Saharan Africa, and they're all at different stages of their academic

career.

Each fellow is paired with two mentors.

Since they've started they have been engaged extensively in grant writing, manuscript preparation

and publication, among other things.

With that, I will turn it to, I believe, Makeda?

>> MARY MCKAY: No, I'll take it one more time to make some summary comments, Ozge.

Thank you.

I guess that I want to sum up, with gratitude to both Ozge and Mary for co-presenting with

me, and I just want to highlight a set of things that our NIH colleagues have been incredibly

supportive but also really challenged us to be bigger than we thought we could be and

to be more ambitious than we thought even possible.

This program of research I just want to underline has really had us engage deeply with policymakers

and funders, both in the U.S. as well as in the continent of Africa, and that those are

a set of needed, critically important, but often not forged relationships between academics

and policymakers.

There are incredibly sophisticated and challenging community-based and collaborative participatory

methods that underpin the formative work and also continually underneath both of these

ambitious efforts.

On top of that, us choosing really innovative, rigorous research designs, choosing to go

a mixed-method set of approaches, and keeping everybody on these teams and these champions

in line in trying to achieve the goals of the study, have been both some of the most

rewarding work of our, at least my life and also the most challenging.

I'm grateful for the opportunity and the support for NIMH.

I'm grateful for everybody that works in both of these very large teams.

I'm happy to, Denny, have you lead us in some questions and know that I'm grateful for your

individual support as well.

>> DENISE PINTELLO: Thank you, Mary, and thank you very much to Mary Acri and Dr. Ozge Sensoy

Bahar.

Those are great presentations.

I'm very excited about the work that you are doing at this time, and I do want to express

my appreciation for the opportunity to join in and facilitate this discussion.

During the next few minutes, I would like to do a quick summary of what we've heard

so far about targets, mechanisms of change, facilitate any discussion and questions, and

invite our participants to submit any questions that you have.

Then also as we close, tell you about related funding opportunities that I hope some of

you are thinking about as you consider applying to NIMH and that hopefully there's something

in there that speaks to your passion for research.

As you saw, a fantastic presentation by Dr. Michael Freed.

He provided an overview of the experimental therapeutics approach, and the gist is that

in services research interventions it's tough to do on our end of the continuum.

It's very easy to identify targets and mechanism of change on the basic science side.

But what we're finding in the last three years, a lot of the researchers have stepped up and

really have provided great targets as far as clinician-, patient-, and consumer-level

targets, clinician- and provider- level behavior, and organizational and system-level factors.

The goal is to try to - what are you targeting?

What are you trying to change and manipulate as you design your study?

Those are some of the pieces that we've been really encouraged by with taking this approach

in the last 5 years, or 4 years about.

As you heard earlier when Mary McKay presented her first study, and you saw the slide that

identified the various levels - your core family variables, provider level, clinic level

- and then you can see targets in between that they're manipulating.

For instance, with the provider level, looking at manipulating motivation, preparedness,

fidelity, and clinic level or organizational level, you're looking at manipulating readiness,

leadership support, and climate through those teams, those implementation clinic teams.

That was a nice way.

I really appreciate you providing that overview.

Then the next study that Ozge and Mary presented about SMART Africa, again just looking just

at that capacity-building piece, the provider level, and some of the targets that they are

manipulating are knowledge, skills, and motivation, and using a number of different activities

to test those and manipulate.

These are some really exciting approaches that we would love to see the results in.

I just want to quickly provide another example.

I know we're kind of tough on time here, but a really wonderful D&I (dissemination and

implementation) research example is from Aaron Lyon who has an R21 titled "Beliefs and Attitudes

for Successful Implementation in Schools," and he is testing a pre-implementation training

intervention designed to improve the delivery of a school-based mental health evidence-based

treatment.

On his figure here, you see he is providing a pre-implementation intervention, he's doing

some training, motivational enhancement training therapy, to manipulate school-based mental

health provider attitudes, perceived behaviors, and subjective norms to see does that influence

their intention to implement.

Then you can see the lineage to does that enhance their ability to deliver the evidence-based

treatment and then hopefully enhance mental health outcomes?

Look at NIH Reporter or feel free to contact Aaron if you have any questions or you'd like

to learn more about his model.

What I'd like to do now is transition to see if anybody who is listening to us today, I

think we have at least nearly 50 folks, that have questions.

I'd like to go ahead and kick us off with a question to Dr. Mary McKay, because you've

been working in the field for a little while I believe, and in 2014 when our experimental

therapeutics approach was initiated at NIMH, it happened to be around the timeframe you

composed your R01.

You were one of the first folks that really put in the targets and mechanisms of change.

I'd love to get a sense of your initial thoughts at that time on the experimental therapeutics

approach, and has this thinking for you changed over time?

>> MARY MCKAY: That's a great question.

I think that the particular way that the call for proposals was written truly challenged

my colleague Kimberly Hoagwood, myself, Mary Acri, to think very specifically about those

mediators and moderators that I presented, and also to think about how on earth we were

going to actually really study them.

The call for proposals probably pushed us to propose a study that we thought was actually

bigger than ourselves.

I think - in retrospect I'm very happy we did that.

At the time that we got the funding, we were both joyous and terrified, because what we

had proposed is to work across an entire system to attempt to sample from every clinic in

New York City, and Mary Acri and team are well on their way from either being able to

actually sample and run groups and collect data in every clinic in New York City, or

deeply understand from directors' and providers' perspectives about the choice not to participate.

I think that the call is very challenging to us as investigators to open up the intervention

packages that Mike so nicely put up in terms of his graphics, make hypothesis based on

the limited preliminary data that we had.

For example, Mary put up some of our hypothesis about we think that some of those Rs are more

impactful than others.

Those come out of some of our post hoc analysis of our trial data.

I'm not sure I would have taken those steps had it not been that the call really challenged

us.

Denny, is that how you kind of wanted me to respond?

>> DENISE PINTELLO: Absolutely.

I really appreciate that because that parallels a lot of feedback that we've received from

the field, because in 2014 it was a new approach.

It was a different way to frame your research questions and design, so I really do appreciate

your thinking and articulating that for us in the audience.

What I'd like to do is ask another question here, and this would be to Mary Acri and to

Ozge Sensoy Bahar.

As folks that are newer to the field than some others, as up-and-coming researchers,

can you speak to your thoughts about the benefits of testing targets and mechanisms of change

in the field of mental health, as well as the challenges?

>> MARY ACRI: Ozge, do you want to lead?

>> OZGE SENSOY BAHAR: You can take it and I'll follow you.

>> MARY ACRI: Sure.

As a relatively newer investigator, this project has been really revolutionary in terms of

my career, and just on back of what Mary had said, to be able to see how an entire service

system responds to recruitment requests as well as uptake.

We're leading something like 15 groups in the fall so far, and so to launch this massive

endeavor on a large scale is just so rewarding.

Also in terms of the mechanisms of change and looking at specific targets, I feel like

it advances the knowledge base as to what are the critical ingredients or the primary

ingredients in terms of why a particular intervention is effective, and are there more ingredients,

to use the same analogy, that are more effective than others?

I think this really moves the field further because we want to unpack - we know that behavioral

parent training programs are effective, but the critical ingredients within them, and

whether there are specific factors that are more effective or more impactful, really is

a new venture.

It's exciting to be part of that.

>> OZGE SENSOY BAHAR: Just to build on what Mary Acri said, I am personally really excited

about the opportunity to see these mechanisms of change and what is similar and what is

different in comparison to the U.S. context.

In Sub-Saharan Africa, I think we have the opportunity because we will be conducting

the intervention in not only three different countries, but also in school systems as opposed

to mental health services systems, I think it will be really fascinating to see what

will look similar and what will look different.

>> DENISE PINTELLO: Thank you very much.

That's great.

We have one question and we have very limited time to respond, but let me go ahead.

We have a question from Kaley Patrick asking about, "Some calls for proposals push to have

investigators apply for and receive an R21 before submitting the R01.

How do you conceptualize an R21 as a building block for an eventual R01 within the context

of building capacity within a low-middle income country?"

This would be for the international side of our group today.

Mary or Ozge?

>> MARY MCKAY: Yeah, I can respond but also maybe Makeda or NIH colleagues, if you want

to think about that as well.

This program of research builds on a whole series of pilot studies, R21, R34, unfunded

work, small grants from our university.

You can trace the building, the learning, the adaptation from a number of studies ahead

of time.

I think the challenge to investigators currently is it feels more complex what has to happen

in your R21 or your pilot studies in order to be able to apply for one of these mechanisms.

You need to know the levers at multilevels.

You at least need your R21.

Your pilot study needs to kind of uncover those, collect some data on what you think

those major feasibility obstacles are, what major targets are, some of the obstacles in

your setting or facilitators in your setting.

I think that the more narrow theoretical frameworks that we might have used in the past for intervention

research, we have to rethink which frameworks we're using to guide the early studies so

that we come away with multilevel data that will inform a more comprehensive, both effectiveness

and implementation, trial.

Am I making any sense, Denny?

Because that's off the top of my head.

>> DENISE PINTELLO: Absolutely.

Then we will follow up with the ... Provide NIMH suggestions for the requester of the

information.

Thank you very much, Mary and everyone.

Before we wrap up, I do want to share some information about some new funding opportunity

announcements that I hope this audience would have some interest in, because it also refers

to the targets and mechanisms of change.

As Dr. Michael Freed discussed earlier, we do have clinical trial funding opportunity

announcements, and these are three that relate to services research and of course hybrid

designs with a D&I, dissemination and implementation, field.

You will find these at our webpage here.

Our Branch, in the Services Research and Clinical Epidemiology Branch, within the last 3 or

4 months has issued these five FOAs.

We're very excited about these.

You will see the first two," Effectiveness Trials for Post-Acute Interventions" and "Services

to Optimize Longer Term Outcomes," those also include you applying for a study that would

have targets and mechanisms of change, and also these are open to foreign entities.

The Mental Health Navigator Model, that is also requiring if you have clinical trial

you have to identify targets and mechanisms of change.

Then the last piece doesn't involve clinical trials, so you don't have to have targets

and mechanisms of change with that.

You'll notice with the first four there's a 2018 expiration date.

Please don't worry.

We're planning to reissue them so they will have a lifetime of 2020, but please contact

myself or Mike Freed if you have any questions.

Mike is our contact for the first two FOAs and I'm the contact for the second.

If you have any additional questions, please feel free to contact us.

The last piece that I'm going to say before I turn it over to our organizers is that we

are very proud to convene a large mental health services research conference.

It's our 24th conference.

Last year Dr. McKay was one of the co-chairs of the conference.

Please put the dates aside for August 1st and 2nd.

It would probably be convened here in the Washington D.C. area, so I just wanted to

let you all know that, and we hope to see you there.

Thank you.

>> MAKEDA WILLIAMS: Thank you so much to all of our speakers today for a very informative

webinar on mental health services research, and thank you to Dr. Pintello at the end for

sharing those FOAs and the conference in August of next year.

That was very well said.

Hopefully those who are on the call will be able to participate.

I'd also like to thank NIMH leadership, the Bizzell Group, and OneSource for their support

of our webinar series and logistics.

Our next webinar will be held on Tuesday, September 12, 2017, from 9:00 a.m. to 10:30

a.m. U.S. Eastern Time.

The title of this webinar is "Research Capacity Building, Nurturing, and Strengthening Emerging

Scientists."

Please visit the Global Mental Health webinar website for more information.

Now I'll turn it back over to Wendy, our operator, to close out today's webinar.

>> WENDY: Thank you.

This does conclude today's program.

Thank you for your participation.

You may disconnect at any time.

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HenryG : "On aura une bonne équipe UK d'ici 2020" - FACEIT London Major 2018 - Duration: 4:37.

For more infomation >> HenryG : "On aura une bonne équipe UK d'ici 2020" - FACEIT London Major 2018 - Duration: 4:37.

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Overwatch 2018 New HALLOWEEN Skins (Ideas, Artwork, & Possible Teasers) - Duration: 10:04.

What's up everybody this is Master Ian Gamer and with the spookiest event of the year drawing

ever closer, now is the perfect time to look at what skins we could be getting for Halloween

Terror.

Halloween boasts some of the greatest potential for new skins, and has historically held some

of the community's all time favorites.

So, let's take a look at some of the coolest, most terrifying new skins we might get with

this year's Overwatch Halloween event!

As always if you end up enjoying this video, then be sure Like, Sub, and hit the Bell to

keep up with all my future Overwatch content.

Now I have to mention real quickly that yes I'm aware of the various leaks we've gotten

for the upcoming event.

In fact, I've already made videos covering them and speculating who exactly they're

for.

But, in this video, I'm more or less going to pretend that the leaks don't exist, and

simply look at skin possibilities that we could see, either this year in addition to

those which were leaked, or perhaps in the future.

But anyways, let's kick it off with Sorceress Moira!

This is one of those skins which feels somewhat inevitable for her, and given that magic and

witchcraft fit perfectly within the scope of Halloween, this seems like the perfect

event to get it.

Her abilities already feel very magical, and her scientist background could easily be compared

to a mythical wizard or sorcerer.

On top of that, this kind of skin would make her the perfect candidate for being a new

Junkenstein's Revenge boss, as I could easily see someone with dark powers like these working

with the Witch of the Wilds and her other minions.

Blizzard could go for either a more scientist-esque skin design like Junkenstein himself, or it

may closer resemble Witch Mercy in terms of using pure, mystical magic.

Either way it'd be a great skin for a hero who so far hasn't gotten many event Legendaries.

Moving on, we have Mummy Genji.

Once again looking at the hero's backstory, Genji nearly died at the hands of his brother

before being saved by Mercy.

He only made it by being fused into a new cyborg body, which he now depends on in order

to survive.

Wrapping his body in white cloth could easily fit with his design, even down to the loose

bit of material which trails behind every one of his skins.

Additionally, his weapons would likely be stylized to fit a more Egyptian theme, as

that is the region with which mummies are often most closely associated.

While we already see a style similar to this in his Nomad skins, Blizzard could easily

add more detail, possibly even designing it to appear more horrific than these other two.

Next up though, we have werewolf Winston.

This is one of those skins that seems good at first, but gets better the more you think

about it!

Sure both of them are large, dark furred beasts so to say, but the real dealmaker for me on

this skin idea is the fact that Winston's Primal Rage fits perfectly for the idea of

a werewolf transformation!

A kind mannered scientist by day, Winston occasionally becomes a ferocious beast, lunging

across the battlefield and swiping at anyone in his path.

While the fact that he's a gorilla doesn't quite coincide with the wolf aspect of a werewolf,

I think it's close enough to work.

His tesla cannon and jump pack could even be stylized to have a 19th century aesthetic,

thus making the skin as a whole fit in with many of the other classic horror story inspired

skins which are already in game.

Next, we have another fitting skin which has been brought up countless times in the community,

and that's Plague Doctor Ana.

Boasting the iconic, beaked mask, and vials of questionable substances, this creepy costume

would fit perfectly within the Halloween event.

Her gun could be stylized into a medieval repeater rifle, and biotic grenade would fit

perfectly as some kind of potion.

While Reaper does already have a Plague Doctor skin, I don't think that would prevent other

heroes from being able to get one.

Besides, Ana seems to fit the concept better, what with her being an old timey, cloak wearing

medic.

And next we have one of my personal favorite skin ideas, and that's Ghostbuster Zarya!

Now, this is an idea that has been floating around since at least last year's event,

and some people even went ahead and made some cool concept images of what this skin might

look like.

The tan jumpsuit and large beam weapon would fit her aesthetic perfectly, and you could

even draw the comparison of her Graviton ultimate to the ghost traps which suck in the pesky

spirits.

The only real issue I see is the copyright restrictions around designing a skin like

this, but I'm sure Blizzard could get away with it if they switched up the jumpsuit design

and called it something like "ghost hunter" instead of "Ghostbuster".

Beyond Zarya though, I could also see this skin being for Winston instead, given that

he also wields a bulky gun which, granted, shoots out electricity instead of… this.

But the comparison is still there.

Also his barrier projector could be considered the ghost trap, and on top of all that he's

already a scientist, which would match up better as a Ghostbuster than a soldier/weightlifter.

Personally though, I still feel like Zarya would be the better choice between the two,

but I could see either working.

Next though, we have two much more comedic Halloween skins, which are cardboard D.Va

and Reinhardt.

Now, these sort of cardboard skins could work for a number of different heroes, but I picked

these two based on their already in game sprays.

Basically the idea behind them is just that they're cheap Halloween costumes made out

of cardboard and duct tape.

Reinhardt's would probably make a little more sense than D.Va's, as a working cardboard

mech is a bit harder to imagine than just a large man strapping boxes to his body.

But regardless, both would be comedically fun skins to have in game, and would definitely

introduce a much more humorous vibe amongst the event's many other horror themed cosmetics.

But, while on the topic of Reinhardt, there are actually two Halloween skins we've seen

for him that don't exist yet in game, being the Admiral and King from the Junkenstein

comics.

Both of these fit him very well and definitely look like something that could be added.

Additionally, three of the other skins we saw in the 2016 comic weren't released until

the 2017 event.

So, who's to say that Blizzard wasn't holding out on one or both of these Reinhardt

skins for just another year?

Now between the two of these skins, I'd have to say that the Admiral seems a bit more

likely to actually make it into the game, since Reinhardt already has some rather kingly

looking skins, so getting another wouldn't feel as special or unique as the seafarer

one.

But, like the Mercy witch skin we see in this same comic, perhaps Blizzard will decide to

change up its actual appearance in game, thus meaning that we could be in for a pleasant

surprise with either of these teased Reinhardt outfits.

Likewise, we also have a Genji Swordsman skin shown in the 2017 Junkenstein comic.

This could certainly be a future Halloween skin as well, and I actually talked about

it a bit more in detail in one of my previous videos which you can check out through the

card on screen.

Shifting back to D.Va though, she in particular has a few good possibilities of her own.

The first of these is simply some kind of jack-o'-lantern, like the concept skin we

can see here.

The mech's size and shape would be perfect as a giant, rideable pumpkin and D.Va herself

could wear some kind of matching attire.

Also, this could easily be a skin for Wrecking Ball as well, given his own mech's spherical

design.

Regardless of which hero it's for, maybe being both, I could also easily see it being

an Epic skin instead of a Legendary.

Changing the mech colors and detailing slightly to better resemble a pumpkin and then just

giving minor detailing to either D.Va or Hammond could make it fit the jack-o'-lantern theme

without needing to greatly remodel the base skin.

Another great idea that could work is Cinderella D.Va.

In this skin, the mech would be stylized more into a pumpkin carriage rather than a straight

up jack-o'-lantern, and D.Va herself would have some kind of fancy princess dress.

Once again, copyright might become a bit of an issue, but for a skin like this I could

see Blizzard generalizing the design enough to work around any limitations.

But moving away from the whole pumpkin motif and considering a very different sort of skin

design for D.Va, we have D.Va the Destroyer.

Now this skin likely sounds familiar to some of you, and that's because it's actually

a skin for her in Heroes of the Storm.

Needless to say, it looks pretty cool and I can't really see anyone complaining if

this were to get added into Overwatch.

Given that Symmetra got her Dragon skin last year, I really see no reason that Blizzard

couldn't add more demonic themed skins into the game, especially for the Halloween event.

It wouldn't have to look exactly D.Va the Destroyer.

The mech in particular I think could be redesigned at least a little, and they'd probably give

the skin a different name.

But in terms of a new skin, this is certainly one which would be both unique and welcome.

Beyond just D.Va, I could see a number of different heroes getting demon themed skins.

People have done some cool concepts for a Demon Orisa, and depending on the level of

detail, some heroes could even just get Epic versions like Hanzo's from back in 2016.

Basically anyone could get something simple like this, so just take your pick!

Now before I wrap up, I will just mention that all these skins are simply based off

of fun ideas that would accurately fit both the event and the specific heroes.

They aren't taking into account which heroes are most likely to get new skins this time

around based off of who's gotten what in the past.

I may make a later video delving into the statistical side, but I did already address

it a little in one of my earlier videos where I discussed the event's start date and some

of the already leaked skins.

Again if you haven't seen that, I'll include a card linking to it for you.

Also, this is by no means all the possible Halloween skins.

I'm sure you guys have a ton of great ideas which I simply haven't thought of, so please

feel free to drop those down in the comments.

If I can collect enough cool ideas, I may even be able to make another skin ideas video

before the event starts!

Also if any of you happen to possess artistic talent, feel free to send me your own Halloween

skin concept drawings.

I might end up showing them off in a future video!

But for now, thank you so much for watching, be sure to leave a like if you enjoyed this

video and share it with a friend if you really liked it!

Subscribe and hit the bell to keep up with all my future Overwatch content, and follow

me on Twitter for fun polls and channel updates.

This is Master Ian Gamer signing off, and until next time have a great day!

For more infomation >> Overwatch 2018 New HALLOWEEN Skins (Ideas, Artwork, & Possible Teasers) - Duration: 10:04.

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For more infomation >> Mitsubishi Colt 1.5 DI-D AIRCO INFORM COOL PACK NW. APK ! - Duration: 0:49.

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Ways You're Probably Ruining A Perfectly Good Cocktail - Duration: 5:12.

When you're out at a bar, you don't have much say over every little detail that goes into

making your cocktail.

That's why some cocktail aficionados will only imbibe these adult beverages at home.

If you'd like to join their ranks, the first step is… well, learning how to avoid ruining

a perfectly good cocktail, of course.

Maraschi-no-no

It shouldn't come as much of a surprise, but those artificially-sweetened, neon-red maraschino

cherries that we stuffed into our virgin drinks as kids are not the most natural ingredient

you can add to a cocktail.

No old-fashioned wants to be sullied by fake sugar syrup.

But there's another kind of maraschino cherry out there the real maraschino cherry, and

you should absolutely be putting those in your cocktails.

Luxardo Maraschino Cherries, said to be the original, are candied with sour Marasca cherry

juice and sugar, without preservatives or coloring.

They're a deep, dark purple-red color, and since all maraschino cherries are not created

equally — it's worth mentioning that they actually taste like cherries.

Really, really good cherries.

Your taste buds and your guests will thank you.

Mixing things up

We all know that Martha Stewart is the queen of entertaining, and therefore we should all

follow her simple piece of advice on how to make a great cocktail.

As she says, "The juice must be fresh.

No mixers, and no Skinny Girl."

Amen, Martha.

When you buy a bottle of sour mix or other mixer off the shelf, you have no idea what

it will taste like.

Plus, chances are, it'll be chock full of additives and preservatives.

You don't want to chance ruining a cocktail with a funky tasting mixer when you can easily

make them at home.

For instance, if you can boil water, you can make simple syrup.

Combine equal parts water and sugar in a saucepan and simmer until the sugar is dissolved.

It's that simple — and most of the internet's endless tips and tricks for making homemade

mixers are just as easy.

Hack your hooch

Super-cheap vodka may have been your go-to shooter in college, but now that you're making

cocktails and you actually care how they taste, those bottom-shelf brands might not be as

good as you remember from your wild party days.

Maybe you still have a bottle in your cabinet though, or maybe you're just the frugal type.

Either way, there's a trick to improve the taste of that crappy, inexpensive vodka.

With the help of a regular ol' water filtration pitcher, your cheap vodka won't taste quite

so cheap.

By pouring it through the pitcher four times, you're replicating the filtration process

of the more costly stuff.

Now, as much as this method will help smooth harsh flavors out, you probably still won't

want to drink it straight.

But according to America's Test Kitchen, when served in mixed drinks in a blind taste test,

it passed with flying colors.

If only you'd known this technique in college, during that jungle juice phase…

All the right moves

James Bond famously preferred his martinis "shaken, not stirred," but that doesn't necessarily

mean it's the correct way to drink them.

"A medium dry martini, lemon peel, shaken not stirred."

"Vodka?"

"Of course."

There is a correct time to shake, and a correct time to stir, and the two methods are not

interchangeable.

As it turns out, Bond's preference would be doing that martini a disservice.

Here's why:

Shaking a cocktail is meant to introduce air into the liquid, which creates a frothy texture

and is necessary when using mixers like citrus or cream-based additions.

This method does cause the ice to break down some in the process, but the dilution helps

balance the flavors of the drink.

Stirring a cocktail is a gentle way to chill the liquid and combine ingredients without

introducing air.

This keeps things silky, dense, and clear.

Generally speaking, cocktails that are made up of all liquor should be stirred, meaning

drinks like martinis and Manhattans stay out of the shaker.

Sorry, Double-O-7.

A muddled mess

Muddling seems like a pretty simple technique: You throw a few ingredients into a glass,

mash them into oblivion, and continue on with your Tom Cruise Cocktail impersonation, right?

Wrong.

There's actually a correct way to muddle, or you run the risk of ruining a perfectly

good mojito.

Believe it or not, there are several things you have to considered when muddling.

For starters, you want to make sure to choose a thick, sturdy glass to make your cocktail.

Second, the muddler itself should be flat-bottomed and unlacquered utensils with teeth on the

end are too rough on herbs.

Lastly, and probably most importantly, know your own strength.

The muddler is not meant to mash mint leaves or other herbs into a puree.

In fact, when you overwork some herbs, like mint, the veins in the leaves release chlorophyll,

which is bitter and will make an otherwise fine cocktail taste like freshly cut lawn.

Tools of the trade

It's time to ditch the red Solo cups, kids.

Sure, they're an easy choice no dishes to wash, unbreakable, great for beer pong but

they're not doing your cocktails any favors when it comes to taste.

Aside from the standard wine and beer glasses, there are a few other cocktail-centric styles

you might want to consider adding to your arsenal:

Martini or, "cocktail" glasses are meant for serving drinks without ice.

Use these for classic martinis, of course, and cocktails that are shaken and strained,

like Manhattans and cosmopolitans.

Rocks or, "lowball" glasses are meant for building drinks in, like the old-fashioned.

These are the cocktails you'll likely stir, not shake, as well as liquor served straight

up.

Highball or, "Collins" glasses are meant for mixed drinks with lots of ice, like a mojito

or bloody Mary.

Not convinced?

Do a martini taste test out of a proper glass and then a red cup, and see if you can't tell

the difference.

For more infomation >> Ways You're Probably Ruining A Perfectly Good Cocktail - Duration: 5:12.

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Protocol Vento Wifi quadcopter 9-24-18

This is another Udi Rc Rebrand just like the Potensic Nova and Wings

Hate that the camera is pointing down this much.....

Thanks for watching please subscribe and hit that like button.......

For more infomation >> Protocol Vento Wi-Fi 9-24-18 - Duration: 6:48.

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For more infomation >> To the Moon and Back | BOOK CLUB - Duration: 1:12.

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For more infomation >> DAS ist der Boss?! - Part 15 - Shin Megami Tensei: Persona 3 FES (PS2) - Duration: 36:21.

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Chasse et C-71 - Bernard Généreux (SO31) - 2018-09-24 - Duration: 1:06.

For more infomation >> Chasse et C-71 - Bernard Généreux (SO31) - 2018-09-24 - Duration: 1:06.

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Introduction - Duration: 0:36.

Hi! This is Amanda Nash with Realty ONE Group in Scottsdale, Arizona. I'd like to

quickly introduce myself. I was born and raised in Colorado. I moved to Arizona in

2004 to be closer to my grandma who first moved to Arizona in the 1940s. I love

Arizona and cannot imagine living anywhere else because of the great hiking, camping,

four-wheeling, and boating it offers. I came to real estate after years of

learning about buildings and construction from my dad who worked in

property management for over 25 years. I really enjoy helping people so thank

you for your time today and I look forward to having the opportunity to

help you find your dream home.

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