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Welcome to the Clinician Researcher podcast, where academic clinicians learn the skills

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to build their own research program, whether or not they have a mentor.

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As clinicians, we spend a decade or more as trainees learning to take care of patients.

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When we finally start our careers, we want to build research programs, but then we find

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that our years of clinical training did not adequately prepare us to lead our research

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program.

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Through no fault of our own, we struggle to find mentors, and when we can't, we quit.

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However, clinicians hold the keys to the greatest research breakthroughs.

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For this reason, the Clinician Researcher podcast exists to give academic clinicians

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the tools to build their own research program, whether or not they have a mentor.

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Now introducing your host, Toyosi Onwuemene.

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Welcome to the Clinician Researcher podcast.

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I'm your host Toyosi Onwuemene, and it is a pleasure to be talking with you today.

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I'm especially excited because I have a special guest today, Dr. Teresa Coles.

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Teresa, welcome to the show.

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Thank you.

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I'm excited to be here.

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So, Teresa, how would you introduce yourself to the audience, especially with regard to

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your role as an academic faculty member?

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Sure.

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So, I am an assistant professor, and I am very interested in measuring health.

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How can we better measure health, particularly quality of life?

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So, Teresa, I first met you, I feel like about a year and a half ago, and at the time we

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met because I was interested in health measurements, specifically patient-reported outcome measures,

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and I would like you to just talk about how different our perspectives were in terms of

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what I was thinking of as a clinician with regard to patient-reported outcome measures

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and how you think about it as the expert.

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Oh, okay.

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Well, let's see what I can remember.

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So, I think one of the first things we discussed at the very beginning was what outcomes do

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we think might be important to patients?

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And there's so many different quality of life outcomes that might be of interest to patients,

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but actually we don't really know.

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So, I think that was one of our very first conversations is which outcomes should we

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focus on and why?

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We could go about measuring all types.

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We can measure like 90 different types of quality of life outcomes, but that would be

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a lot to have patients to do.

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So, we try to focus in on what are the most important ones for them.

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Sure.

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So, one of the things that I thought about was using something like the SF-36, for example,

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in my population.

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And you talked about the need to have validity evidence to be able to use it in my specific

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population.

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And I was thinking, validity, what?

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So, I want you to speak about that.

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Speak about the fact that there are all these, I mean, they're validated or they have validity

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evidence, but they may not have it in the disease in which I'm interested in.

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How should clinicians be thinking about these tools as they're trying to use them in their

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research?

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Yeah.

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Thank you for bringing that up.

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So, here's the situation.

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There are a lot of questionnaires, patient reported outcome measures, clinical outcomes

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assessments out there.

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And just because they exist or even if they've been used in various populations successfully,

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that doesn't mean that they have enough validity evidence for every single use case.

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So, for example, we might have a patient reported outcome measure or questionnaire that is working

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really well for folks who are 65 and older with some sort of physical functioning issues.

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Okay.

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We may not be able to take that same exact questionnaire and apply it to adolescents.

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And the reason for that is because these individuals will have different types of, let's say, physical

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functioning impairments or issues.

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And if we're asking questions that are not relevant to that patient, then we end up with

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biases and we will not be actually measuring the right things.

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And then we miss an opportunity to intervene and help folks with their quality of life.

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That's a really great point.

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Now I recognize it because we've worked together and you've taught me a lot.

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But what I do see is a lot of people like, for example, the SF-36, maybe one of the more

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widely used ones, why would it be a problem to just take it and apply it to your population,

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especially because it's just so widely used?

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Yeah.

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So there's nothing wrong with SF-36.

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I like the SF-36.

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The strength of the SF-36 is also its limitation.

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So the SF-36 is very broad.

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It's used to look at general quality of life.

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That's great if you want to detect general quality of life.

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If you want to look at specific quality of life impacts based on a particular treatment

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or particular condition, something like the SF-36 may not be able to detect those changes

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or the very specific issues that patients experience.

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So one example we use a lot in the class that Kristi Ziegler and I teach is fatigue, for

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example.

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Somebody might say that they're fatigued.

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Okay.

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Well, there's a thousand different measures we can use to evaluate fatigue.

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But are we looking at physical fatigue?

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Are we looking at emotional fatigue, mental fatigue?

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Unless we actually know what those experiences are, we can't measure them effectively.

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So SF-36 is great at measuring those broad experiences, but it also is so broad it may

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not be able to detect the specific experiences we're looking for.

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So both its kind of strength and its weakness.

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Okay.

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Okay, Teresa, it sounds pretty complicated.

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So why should a clinician researcher think about working with an expert like you if they're

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trying to use patient reported outcome measures in their projects?

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So there are some best practices and how do I say this?

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You're going to have to cut this out.

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Why would you want to work with somebody like myself?

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Because you're awesome.

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Well, one of the reasons is because folks like myself who are trained in health measurement

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know the methodologies, which include both qualitative and quantitative psychometric

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methodologies to ensure we're measuring what it is that we actually want to measure.

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If we do not approach measurement with this type of rigor, we risk bias in how we measure.

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So we may have great sample sizes and we're measuring something, but we don't actually

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really know what that is.

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We also risk the potential of missing information.

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So we may not be able to detect changes based on treatment or changes based on a condition

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that we need to intervene on.

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Thank you.

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Thank you for highlighting what's important, why it's important.

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I mean, because honestly, before we started working together, I really just thought, you

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know, you take a measure and there's no reason why you couldn't use it.

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But really there's a whole science behind it.

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You are clearly a measurement expert and you've been doing this for a long time.

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And so one of the things you highlight is just the need for collaboration.

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So I'm really excited to talk about collaboration.

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So I want to say, Teresa, that it's been an amazing opportunity for me to work with you

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as a fellow researcher, as we've submitted some projects.

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And one of the things I thought it was really just important to highlight is why should

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clinicians and PhD trained researchers work together?

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Oh my gosh.

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The reasons are endless.

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So I think I'll start with like a personal example.

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For somebody like that, myself that's trained in methodology specifically, we're great at

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coming up with methods, but we are not great at knowing what the clinical problems are.

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So where are the opportunities to actually use those methods and make a difference?

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So we often have what we call hammers, right?

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So like we might want to use the same hammers of methodologies across many studies.

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That's fine.

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But really at the end of the day, that's not the most important thing.

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The most important thing is that we're pushing science forward clinically and we're causing

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improvement in quality of life and survival for patients.

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So in order for us to like meet the needs of that issue, we have to collaborate with

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clinicians who know what the issues are.

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Not only that, but the clinicians kind of throughout a project, like for example, when

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I collaborate with clinicians on a project, they keep it centered on the clinical issues

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and the clinical relevance of what it is that we're doing.

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So what are some patient experiences?

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What are clinical experiences?

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The clinicians also have direct contact with patients.

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So how might we recruit patients?

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They also have knowledge of what do the results actually mean, right?

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So we, you know, like from a methodological standpoint, we have a certain perspective

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on what these results might mean and we can provide percentages and tell you about IRT

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loadings.

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Like we can tell you all sorts of things, but at the end of the day, what does it mean?

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How do we interpret those results?

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And I think that's extremely important to work with clinicians on.

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Absolutely.

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You know, one thing you said reminded me of something that's come up before is the difference

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between developing a measure with developing validity evidence for a measure for clinical

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use versus for like a clinical trial.

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Can you just speak to that difference?

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Sure.

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So there's a lot of common methodologies we would use for measures that we might use in

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clinical care versus clinical trials.

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It's all about the use case.

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So in clinical trials, typically we would use, let's say, a patient reported outcome

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measure to look at some sort of quality of life outcome over time and answer the question

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whether the treatment is making a difference, improving or worsening whatever that outcome

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is, or maybe not doing either of those.

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Maybe that outcome is just staple.

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That's like the primary use case in clinical trials and that could be a primary endpoint,

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secondary endpoint, exploratory endpoint.

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Another use case in clinical trials is screening.

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You can use a patient reported outcome measure to screen individuals for participation in

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the trial, so like inclusion and exclusion criteria.

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How we set up the PRO measure and provide the validity evidence for those two different

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use cases requires two different types of methodologies.

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So that's just even within clinical trials.

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And then we look at clinical care, there's lots of different ways we can use patient

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reported outcome measures.

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One is, similar to clinical trials, we can track patients' outcomes over time.

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One additional thing we might do in clinical care is not only continually track those outcomes

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over time, but identify specific instances for specific patients when they've either

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decreased or increased on an outcome in an unacceptable way, where we know some sort

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of intervention needs to take place.

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That is a really important clinical care application and requires particular methods.

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Same thing, so like most of us are familiar with something like the PHQ-9, which is a

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depression screener.

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That is something that we use in clinical care and the methodologies behind something

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like the PHQ-9 are unique to screeners.

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So do you want me to talk about the different methodologies or shall I stop there?

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Please, I'm learning a lot and I do feel it's important because it's nuanced, so I think

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it's helpful to know.

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Sure.

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So I wish I had my slides so I could show everybody.

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So for clinical trials, anytime we're looking at outcomes over time, we are interested in

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lots of different types of evidence.

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That evidence is based on what is the use case.

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So if we're looking at something over time, we first need to ensure that we're measuring

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what we think we're measuring.

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That's a type of validity.

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We need to look at how we might score that measure and what would the scores actually

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mean.

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That gets into methodologies for understanding what we call the dimensionality of that measure.

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So how many scores might there be coming out of that measure?

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For example, the SF-36 has multiple different types of scores for different dimensions of

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quality of life.

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Another thing we need to look at if we're looking at scores over time is reliability.

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So can we be sure that if somebody is, let's say, rated a 33 on day one and they have no

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change in their quality of life by day seven, are they still going to be a 33 or somewhere

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close to that?

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That is ensuring that type of reliability is called test-retest reliability.

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Another important aspect if we're measuring quality of life over time is being able to

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detect change.

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So just like with a thermometer, if I get a fever, that thermometer we hope is going

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to detect that fever, right?

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If it doesn't, we have problems.

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Same thing with quality of life measures.

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If we see an improvement or a worsening in quality of life, we use methodologies to be

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able to ensure that we can detect that change.

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Finally, all of this kind of filters into the final issue, which is how do we interpret

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those scores?

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So at the end of the day, all the methodology that we're using is all based in supporting

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the interpretation of those scores from the measure.

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We cannot interpret or we can't do a great job of interpreting scores if we don't have

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evidence to prove that they're reliable or we don't have evidence to show that we're

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able to detect change over time or if we don't have evidence to show what is the dimensionality

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of our measure, what is it that we're actually measuring?

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So that's just one example in clinical trials.

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Those are typical things that we'll look for.

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That's really excellent.

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Thank you for summarizing that.

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That was really, really well summarized and clearly you've been doing this a long time.

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So for a clinician like me who says, okay, I want to work with a health measurement expert

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like you, what kinds of questions should I be asking and what kinds of things would you

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want to know to help decide if this collaboration makes sense?

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Oh, great question.

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So I think the key piece about working with folks who are health measurements focused

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is one, learning what their interests are.

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Some of us, for example, specialize in different types of populations.

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So I typically work in studies that focus on adults.

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Some of my colleagues focus on pediatric patients.

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Those are slightly different methodologies that we might use to address these different

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populations and how we might ask questions about quality of life for a three-year-old

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versus an 18-year-old versus a 45-year-old.

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Another piece is some of us have a lot of experience in certain conditions or diseases.

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So for example, at UNC, there are a number of people who are really focused in cancer

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and have lots of expertise on measuring quality of life specifically in cancer populations.

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Some of us are more generalists.

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So it's like, what is our background and where are we coming from and then how can we contribute

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to the study?

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So another piece is I would say in most studies where we're doing prospective data collection,

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there's some sort of measurement component.

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And a collaboration with a measurement colleague may be really small where that person is just

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kind of like providing advice.

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And they may not even actually be under study.

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They just may be behind the scenes giving you some ideas.

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And then all the way up to something like a co-PI, which is what you and I have done

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before.

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So as a co-PI, those would be very measurement specific studies where we are trying to optimize

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measurement of some sort of quality of life outcome.

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I also think another question that clinicians might want to bring to the table with potential

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health measurement colleagues is what level of involvement do they like to have?

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So that helps to kind of like focus in on I think the size of the study that you can

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pull off and what types of studies you can move forward.

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And a third thing that I would recommend is if that health measurement researcher is not

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the right person, then who else might be because there's so many connections among all of us

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and we have a good sense, like a telephone book in our heads of who's an expert in X,

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Y, or Z, and then we can connect to you with the right health measurement person.

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That's good.

264
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That's good.

265
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Thank you for sharing that.

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I wonder from your perspective in working with clinicians, what are some concerns that

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you have?

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I think at the get-go, sometimes clinicians don't have a sense for kind of like the best

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practices for health measurement.

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So unfortunately, sometimes a lot of our fundamental work to get a study up and running measurement-wise

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takes a lot of time.

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So there's like formative qualitative work or formative literature reviews that need

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to happen and that just sucks out a lot of time where clinicians feel like they could

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just move forward really quickly and just throw some patient-reported outcome measures

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or COAs into a trial or in clinical care.

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People do that all the time.

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I think, and sometimes it's fine because that measure has already has validity evidence.

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But a lot of times, well, I'm not going to say a lot of times, sometimes it's not okay.

279
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So I don't even remember what the question was anymore.

280
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Just concerns that you have about working with clinicians.

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Well, I love working with clinicians.

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I absolutely love working with them because they keep me focused on what are the actual

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issues.

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I can go down my circles and caves of measurement ideas and math and qualitative inquiry, but

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at the end of the day, is that really going to make a difference?

286
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So I feel like the clinicians help keep me centered on what are the actual clinical issues

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that are going to move us forward in terms of outcomes of research.

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So how are we going to improve patient's quality of life?

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I like that.

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So it's almost like what you're really speaking to is the fact that you're a partner in the

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work.

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And earlier you started talking about the speed to move forward because there's a sense

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that starting the project and administering the outcomes, administering the PRO measures

294
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is the most important thing.

295
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But really there is a need for clinicians to understand that there's a lot of foundational

296
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work that may not feel like active work, but is really important so that when they're moving

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forward with the big clinical trial, it's valid.

298
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And that the questions that they're asking, the answers they're getting are actually answers

299
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to the questions they want.

300
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They want.

301
00:20:23,520 --> 00:20:24,520
Yeah, absolutely.

302
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But formative work, it's like underpinning rigor that will pay off the dividends when

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you want to use those data over and over again or continue to expand your project or your

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research program.

305
00:20:37,400 --> 00:20:44,280
Okay, so it's worth doing it well, especially the first time you're trying to get evidence

306
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for a measure.

307
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I love it.

308
00:20:46,280 --> 00:20:51,960
Okay, so Teresa, one of the things that I think we come up against is that this kind

309
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of work when it comes to PRO measures is not necessarily, I think, as well-funded as perhaps

310
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if we came in just proposing a clinical trial doing some other things.

311
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So I'm curious to know what kind of funding opportunities may exist a clinician researcher

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should be thinking about for this kind of work.

313
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Great question.

314
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So here's the deal.

315
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Here's what I have learned slowly over time, primarily in schools of public health or population

316
00:21:25,240 --> 00:21:32,160
health or schools of medicine, what we find is that there's an emphasis on getting funded

317
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through NIH, and that is fantastic.

318
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The deal with NIH is that they're typically looking for studies that improve patient outcomes.

319
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So that could include quality of life outcomes, right?

320
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A lot of times, methodological work is not actually improving the outcome.

321
00:21:54,200 --> 00:21:59,120
It's helping us better assess whatever that quality of life outcome is.

322
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So for studies like what I do, NIH, sometimes we can get funded by NIH depending upon what

323
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is the focus of that RFA.

324
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But it's often not our biggest funder.

325
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Other funders include a myriad of options, and I feel like there's more that I haven't

326
00:22:20,680 --> 00:22:24,640
even discovered yet, but one is FDA.

327
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So FDA is very interested in methodological rigor for the use in clinical trials so that

328
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we're evaluating patient reported outcomes that are meaningful to the patient and with

329
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rigor.

330
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So FDA has what they call the broad agency announcement that comes out in the fall of

331
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every year, and that is a big honking proposal.

332
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So there's two stages to that.

333
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There is a 10-pager, sort of like a LOI, like a letter of intent, and then there's a 50-pager

334
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if you get invited to do the full thing.

335
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And that's just volume one because there's also volume two.

336
00:23:09,960 --> 00:23:19,520
However, the VA's, and I've had two of them, are a really great way to focus in on methodological

337
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issues.

338
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And FDA loves it because they want to support rigor in clinical trials for outcomes measurement.

339
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They're very supportive of that.

340
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Another opportunity with FDA for some institutions is the FDA CERC.

341
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So some institutions, including Duke, UNC, NC State, were in a CERC, and there's other

342
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CERCs with like, I think Yale has one, Mayo has one.

343
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These are opportunities to work directly with FDA and address kind of like smaller research

344
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opportunities.

345
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Maybe I would say between 250,000 to 750,000-ish in size, but they are more frequently coming

346
00:24:03,040 --> 00:24:05,200
through and really great opportunities.

347
00:24:05,200 --> 00:24:06,920
Oh, you'll have to tell us.

348
00:24:06,920 --> 00:24:07,920
What is CERC?

349
00:24:07,920 --> 00:24:09,600
What does that stand for?

350
00:24:09,600 --> 00:24:13,440
Centers of Excellence in Regulatory Science and Innovation, CERCs.

351
00:24:13,440 --> 00:24:14,440
Okay.

352
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So that's University of Maryland, Johns Hopkins, Yale, Mayo, University of California, San

353
00:24:21,520 --> 00:24:22,520
Francisco, and Stanford.

354
00:24:22,520 --> 00:24:29,720
So if any of your listeners are in those institutions, and Duke, and UNC, and NC State, then you're

355
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covered by a CERC.

356
00:24:31,160 --> 00:24:33,800
Yeah, so there's a few of us.

357
00:24:33,800 --> 00:24:34,800
Okay.

358
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Okay.

359
00:24:35,800 --> 00:24:36,800
Okay.

360
00:24:36,800 --> 00:24:41,840
So FDA is a potential funder and thinking about these CERC opportunities, if your institution

361
00:24:41,840 --> 00:24:45,600
is connected to that, what are their opportunities?

362
00:24:45,600 --> 00:24:47,880
Another opportunity is PCORI.

363
00:24:47,880 --> 00:24:55,200
So PCORI focuses on comparative effectiveness research.

364
00:24:55,200 --> 00:25:00,440
So if you are doing a study that might be comparing different interventions and looking

365
00:25:00,440 --> 00:25:04,760
at those outcomes, that might be a good fit for you.

366
00:25:04,760 --> 00:25:08,360
We've looked at the engagement awards together.

367
00:25:08,360 --> 00:25:11,640
Actually one of the things that I did not mention before that's really important to

368
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methodologies for health measurement is inclusion of patients and other stakeholders in what

369
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you're doing.

370
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So a lot of times we have stakeholder panels to kind of guide our measurement approaches,

371
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and PCORI is really a great funder for those types of opportunities.

372
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Other funders include industry.

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So I'm actually working with David Leverins from Duke.

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He's funded by Pfizer and supporting him on a project where we're developing a super short

375
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questionnaire for use in clinical care.

376
00:25:47,520 --> 00:25:50,960
Sometimes there's AHRQ.

377
00:25:50,960 --> 00:25:53,760
Typically those are very health services related.

378
00:25:53,760 --> 00:26:04,480
So if you have a health services project, let's say you are going to improve resource utilization

379
00:26:04,480 --> 00:26:11,000
using your patient reported outcome measure AHRQ might be a great fit.

380
00:26:11,000 --> 00:26:12,000
That's cool.

381
00:26:12,000 --> 00:26:13,000
Thanks, Teresa.

382
00:26:13,000 --> 00:26:20,480
So NIH, we all know, but also looking at FDA, the PCORI and then industry as well and AHRQ.

383
00:26:20,480 --> 00:26:21,480
Awesome.

384
00:26:21,480 --> 00:26:22,480
Oh my goodness.

385
00:26:22,480 --> 00:26:23,480
It's so funny.

386
00:26:23,480 --> 00:26:25,800
When you started out, you were like, oh, there's lots of options.

387
00:26:25,800 --> 00:26:26,800
I'm like, what?

388
00:26:26,800 --> 00:26:28,800
There are lots of options, but it's good.

389
00:26:28,800 --> 00:26:29,960
It's good to know because you're right.

390
00:26:29,960 --> 00:26:35,280
I think as clinician researchers, we're really focused on NIH and really thinking about which

391
00:26:35,280 --> 00:26:39,360
funder really aligns with what you're looking at.

392
00:26:39,360 --> 00:26:46,200
And it sounds like clinicians and researchers should think about these other potential opportunities.

393
00:26:46,200 --> 00:26:47,200
That is great.

394
00:26:47,200 --> 00:26:48,200
Okay.

395
00:26:48,200 --> 00:26:56,680
So I'm wondering what question should I ask you as someone who's a measurement expert

396
00:26:56,680 --> 00:27:01,280
and I'm a clinician researcher, what question should I be asking you that I might not think

397
00:27:01,280 --> 00:27:02,280
to ask you?

398
00:27:02,280 --> 00:27:03,280
Oh, let's see.

399
00:27:03,280 --> 00:27:14,200
Are you thinking about for like grant submission, study design, what might be happening in clinical

400
00:27:14,200 --> 00:27:15,200
care?

401
00:27:15,200 --> 00:27:20,960
I think all of the above because what I'm hearing you say is that your work is relevant,

402
00:27:20,960 --> 00:27:25,060
not just for research, but even in clinical care as well.

403
00:27:25,060 --> 00:27:27,000
And so maybe we should ask the question two ways.

404
00:27:27,000 --> 00:27:34,200
Maybe the first question is as a clinician, what should I be thinking about and what questions

405
00:27:34,200 --> 00:27:38,500
should I ask my health measurement person who's at my institution that may be relevant

406
00:27:38,500 --> 00:27:39,960
to me in the clinical space?

407
00:27:39,960 --> 00:27:41,540
Oh yeah.

408
00:27:41,540 --> 00:27:48,760
So in the clinical space, one really great kind of low-hanging fruit is to work with

409
00:27:48,760 --> 00:27:54,160
health measurement experts to look at questionnaires you might already be administering in clinical

410
00:27:54,160 --> 00:27:55,760
care.

411
00:27:55,760 --> 00:28:00,240
Are they actually up to the task of doing whatever it is that you want them to do?

412
00:28:00,240 --> 00:28:01,240
Right?

413
00:28:01,240 --> 00:28:06,840
The health measurement expert will give you the support to be able to look at the evidence

414
00:28:06,840 --> 00:28:13,080
as there for those measures and also how you can use those scores to kind of support decision

415
00:28:13,080 --> 00:28:17,680
making within clinical care.

416
00:28:17,680 --> 00:28:24,880
Another opportunity or question that you could work with health measurement folks on is what

417
00:28:24,880 --> 00:28:30,860
questionnaires might I want to administer in clinical care?

418
00:28:30,860 --> 00:28:35,280
And then I can guarantee you that the health measurement person is going to ask you, well,

419
00:28:35,280 --> 00:28:37,400
how would you want to use the scores?

420
00:28:37,400 --> 00:28:38,440
Okay?

421
00:28:38,440 --> 00:28:44,920
So there are a lot of really great opportunities to incorporate screeners in clinical care

422
00:28:44,920 --> 00:28:48,680
to identify patients that really need help at that time.

423
00:28:48,680 --> 00:28:55,960
So if there is, for example, a symptom that you need to know more about, maybe it's pain,

424
00:28:55,960 --> 00:29:02,040
maybe it's itch, we can either implement or identify questionnaires that might help you

425
00:29:02,040 --> 00:29:04,320
be able to do that quickly.

426
00:29:04,320 --> 00:29:12,680
And then a third question that's a little bit more broader is, you know, tell us about

427
00:29:12,680 --> 00:29:17,920
your research program and then where might health measurements kind of support and help

428
00:29:17,920 --> 00:29:21,840
the rigor of what it is that you're trying to do?

429
00:29:21,840 --> 00:29:22,840
I love it.

430
00:29:22,840 --> 00:29:26,280
You know, the first one of the thoughts that came to my mind is, you know, our patients

431
00:29:26,280 --> 00:29:30,200
are sitting in the waiting room on an awful long time.

432
00:29:30,200 --> 00:29:35,600
And so could there be a measure that's actually relevant and valid for that particular question

433
00:29:35,600 --> 00:29:40,040
that the clinician has that they could fill out in the waiting room that actually contributes

434
00:29:40,040 --> 00:29:43,760
to the information the clinician needs to help further their care?

435
00:29:43,760 --> 00:29:50,280
Yeah, that is literally the best time to get patients to ask questions.

436
00:29:50,280 --> 00:29:54,840
We've seen it anecdotally and we've also like evidence about that that's published.

437
00:29:54,840 --> 00:29:55,840
Great.

438
00:29:55,840 --> 00:29:56,840
Okay.

439
00:29:56,840 --> 00:29:57,840
Okay.

440
00:29:57,840 --> 00:29:59,080
How about how about research?

441
00:29:59,080 --> 00:30:00,080
What questions?

442
00:30:00,080 --> 00:30:03,840
I mean, I think we touched on a lot of them earlier, but what question is on asked that

443
00:30:03,840 --> 00:30:06,880
we should we should definitely make sure people are considering?

444
00:30:06,880 --> 00:30:13,280
Well, I'll tell you what's asked that I would like for people to potentially consider modifying.

445
00:30:13,280 --> 00:30:21,560
So people, people might come to us and say, what questionnaire should I include in my

446
00:30:21,560 --> 00:30:23,320
research program?

447
00:30:23,320 --> 00:30:26,000
And it's that's not really the question to be asking.

448
00:30:26,000 --> 00:30:34,280
The question is, how can I measure this thing that I want to measure?

449
00:30:34,280 --> 00:30:38,080
Because it's not so much about it is about the questionnaire, but more importantly, it's

450
00:30:38,080 --> 00:30:40,760
about what it is that you're trying to measure.

451
00:30:40,760 --> 00:30:48,660
So one thing that I would like to communicate is that it's like I don't have a Rolodex of

452
00:30:48,660 --> 00:30:53,720
questionnaires on my desk where I can say, oh, yeah, you know, here's the 50 measures

453
00:30:53,720 --> 00:30:56,720
on fatigue and let's choose one of them.

454
00:30:56,720 --> 00:31:01,880
There's a lot of work that goes into choosing the most appropriate measure for any given

455
00:31:01,880 --> 00:31:02,880
circumstance.

456
00:31:02,880 --> 00:31:07,800
A lot of that is just background literature review, reading what evidence is there, what

457
00:31:07,800 --> 00:31:13,280
work has already been done, and then what we also what we know about our population

458
00:31:13,280 --> 00:31:19,760
of interest and then how that matches to what the questionnaire is actually evaluating.

459
00:31:19,760 --> 00:31:21,760
That is so, so awesome.

460
00:31:21,760 --> 00:31:26,280
And to be honest, I started laughing because I was like, yeah, that's what I thought.

461
00:31:26,280 --> 00:31:32,040
I thought you just you know, all the questionnaires that are out there.

462
00:31:32,040 --> 00:31:33,040
I do.

463
00:31:33,040 --> 00:31:38,760
I think that's a common I think this is a common misperception, you know, misperception, because

464
00:31:38,760 --> 00:31:43,200
I think some people think that we're kind of like librarians of instruments and we're

465
00:31:43,200 --> 00:31:44,200
not.

466
00:31:44,200 --> 00:31:45,200
Thank you.

467
00:31:45,200 --> 00:31:49,000
Thank you for clarifying that you're not.

468
00:31:49,000 --> 00:31:53,800
OK, so what I should do is ask the question is be clear about what I want to measure.

469
00:31:53,800 --> 00:31:56,440
OK, let's use fatigue as an example.

470
00:31:56,440 --> 00:31:59,320
OK, if I say I want to measure fatigue, is that fatigue?

471
00:31:59,320 --> 00:32:01,900
Is that enough?

472
00:32:01,900 --> 00:32:05,320
So here's some of the questions that I will ask you.

473
00:32:05,320 --> 00:32:11,040
If you tell me you want to measure fatigue, I will ask you, well, what is it that you'd

474
00:32:11,040 --> 00:32:12,460
need to know about fatigue?

475
00:32:12,460 --> 00:32:14,560
What is the purpose of measuring?

476
00:32:14,560 --> 00:32:15,560
Right.

477
00:32:15,560 --> 00:32:16,560
Is this a clinical care application?

478
00:32:16,560 --> 00:32:19,280
Is this clinical trials, clinical research?

479
00:32:19,280 --> 00:32:22,400
How often do you want to measure fatigue?

480
00:32:22,400 --> 00:32:25,280
How do you want to use those scores to make decisions?

481
00:32:25,280 --> 00:32:28,660
I think that's like that final question is like zing.

482
00:32:28,660 --> 00:32:31,040
That's what really gets us the answer.

483
00:32:31,040 --> 00:32:37,680
So that helps us really define and zone in to be able to get you the measure that is

484
00:32:37,680 --> 00:32:38,920
going to be most useful.

485
00:32:38,920 --> 00:32:39,920
Sure, sure.

486
00:32:39,920 --> 00:32:41,400
So I'm hearing that.

487
00:32:41,400 --> 00:32:44,600
So you want to, you know, you want to understand the concept you want to measure.

488
00:32:44,600 --> 00:32:48,360
So for example, fatigue, but you also want to be clear about why you want to measure

489
00:32:48,360 --> 00:32:53,320
it, what you're going to do once you find the fatigue and how you're going to respond

490
00:32:53,320 --> 00:32:54,320
to that.

491
00:32:54,320 --> 00:32:55,320
Yeah, absolutely.

492
00:32:55,320 --> 00:32:56,320
OK, all right.

493
00:32:56,320 --> 00:32:57,320
This is very nuanced.

494
00:32:57,320 --> 00:33:00,840
OK, everybody who's listening, if you are trying to use a patient report at outcome

495
00:33:00,840 --> 00:33:05,080
measure in your study, you got to get with an expert.

496
00:33:05,080 --> 00:33:07,200
And they all have this amazing network.

497
00:33:07,200 --> 00:33:09,440
So if you find one, they can find you the right person.

498
00:33:09,440 --> 00:33:13,360
OK, I think there's one more thing I want to ask, because I feel like this is something

499
00:33:13,360 --> 00:33:18,080
that I learned from you too, is so when I think about patient report outcome measures,

500
00:33:18,080 --> 00:33:21,200
I just think of them as just, oh, it's patient reported outcome measures, and they're so

501
00:33:21,200 --> 00:33:22,200
important.

502
00:33:22,200 --> 00:33:27,280
But really, there's a bigger context of clinical outcome assessments under which patient reported

503
00:33:27,280 --> 00:33:30,240
outcome measures are a subset.

504
00:33:30,240 --> 00:33:35,940
So can you just speak to the broader perspective of clinical outcome assessment and how maybe

505
00:33:35,940 --> 00:33:39,520
patient reported outcome measures may not be what we want to use?

506
00:33:39,520 --> 00:33:41,440
Yeah, absolutely.

507
00:33:41,440 --> 00:33:49,360
So I think patient reported outcome measures are typically the most often discussed type

508
00:33:49,360 --> 00:33:52,760
of clinical outcome assessment, but there are so many more.

509
00:33:52,760 --> 00:33:57,440
So actually, on FDA's website, there's a really nice set of definitions for each of these

510
00:33:57,440 --> 00:33:59,660
assessments, but I'll give you an overview.

511
00:33:59,660 --> 00:34:05,360
So we think about clinical outcomes assessments, these are ways that we can measure patient

512
00:34:05,360 --> 00:34:06,360
outcomes.

513
00:34:06,360 --> 00:34:10,120
OK, so there's four primary ways we can do it.

514
00:34:10,120 --> 00:34:15,000
And for some quality of life outcomes, we can use all four of these ways.

515
00:34:15,000 --> 00:34:17,800
So let me go through each one of those, and then we'll talk about it more.

516
00:34:17,800 --> 00:34:22,580
So one that we've already discussed is patient reported outcome measures, or PROMs.

517
00:34:22,580 --> 00:34:25,920
Another one is observer reported outcome measures.

518
00:34:25,920 --> 00:34:28,360
So that is where we are OBSRO.

519
00:34:28,360 --> 00:34:35,160
So that is where an observer tells us about a patient's signs.

520
00:34:35,160 --> 00:34:41,260
So what can they observe about how a patient is functioning, for example?

521
00:34:41,260 --> 00:34:45,760
Another type of clinical outcome assessments that I'm sure a lot of the clinicians here

522
00:34:45,760 --> 00:34:47,440
are used to are ClinRose.

523
00:34:47,440 --> 00:34:50,160
So clinician outcomes assessment.

524
00:34:50,160 --> 00:34:54,440
So that's a clinician reported measure, and there are a number of those in clinical care.

525
00:34:54,440 --> 00:34:59,960
So for those in cancer, like the ECOG, for example, is a clinician reported outcome measure.

526
00:34:59,960 --> 00:35:03,480
Finally, there's performance measures, or PRFOs.

527
00:35:03,480 --> 00:35:08,180
So those are opportunities to essentially test patients on their functioning.

528
00:35:08,180 --> 00:35:15,760
So like the six minute walk test, or stand up and go, those are examples of PRFOs.

529
00:35:15,760 --> 00:35:20,760
All four of those types of clinical outcomes assessments can be used to evaluate patient

530
00:35:20,760 --> 00:35:25,760
health status, and they can be used as primary, secondary, exploratory outcome measures in

531
00:35:25,760 --> 00:35:30,360
clinical trials, or even obviously for use in clinical care as well.

532
00:35:30,360 --> 00:35:33,320
We use these all in clinical care all the time.

533
00:35:33,320 --> 00:35:38,820
The choice of which one of those you use depends upon what it is that you're measuring and

534
00:35:38,820 --> 00:35:40,080
why you're measuring it.

535
00:35:40,080 --> 00:35:43,320
How are you going to use those scores?

536
00:35:43,320 --> 00:35:44,320
That's really good.

537
00:35:44,320 --> 00:35:45,320
That's really good.

538
00:35:45,320 --> 00:35:46,320
Okay.

539
00:35:46,320 --> 00:35:47,320
All right.

540
00:35:47,320 --> 00:35:51,320
So we're at the end of the show, and the last question on my mind, which to some extent

541
00:35:51,320 --> 00:35:58,040
you've answered, but so if there's a clinician researcher out there who's now like, whoa,

542
00:35:58,040 --> 00:36:08,920
I had no idea, where should they start first as they investigate using patient reported

543
00:36:08,920 --> 00:36:12,840
outcome measures or other clinical outcome assessments in their projects?

544
00:36:12,840 --> 00:36:14,000
Wow.

545
00:36:14,000 --> 00:36:22,400
So I think the first thing that I would recommend for that clinician to do is get clear on what

546
00:36:22,400 --> 00:36:26,360
are the outcomes that you think would be important to measure and why.

547
00:36:26,360 --> 00:36:34,560
The next thing that I would do is contact somebody who works in health outcomes.

548
00:36:34,560 --> 00:36:36,620
Sometimes that's fellow clinicians.

549
00:36:36,620 --> 00:36:41,840
There's a lot of fantastic clinician researchers out there who are doing work specifically

550
00:36:41,840 --> 00:36:43,980
in clinical outcomes assessments.

551
00:36:43,980 --> 00:36:45,480
Sometimes it's a clinician.

552
00:36:45,480 --> 00:36:49,880
Sometimes it's PhD trained researcher like myself.

553
00:36:49,880 --> 00:36:52,280
At Duke, for example, we have the Center for Health Measurement.

554
00:36:52,280 --> 00:36:57,240
All of us that are in the center are interested in measuring health and trying to improve

555
00:36:57,240 --> 00:36:59,720
the accuracy of how we do it.

556
00:36:59,720 --> 00:37:05,480
So you can look for somebody who has a background in psychometrics, for example, somebody with

557
00:37:05,480 --> 00:37:11,160
health measurement or questionnaire design background.

558
00:37:11,160 --> 00:37:17,480
The ideal situation is that person either has both qualitative experience and psychometric

559
00:37:17,480 --> 00:37:23,520
experience or has one or the other and then knows somebody else who does the other one.

560
00:37:23,520 --> 00:37:27,240
And just have informal conversations with these folks.

561
00:37:27,240 --> 00:37:32,960
When I first came to Duke, one of my collaborators that I'm now working with now, the whole way

562
00:37:32,960 --> 00:37:37,040
we started collaborating with each other was just random conversations.

563
00:37:37,040 --> 00:37:38,040
That's how we started.

564
00:37:38,040 --> 00:37:43,200
We were thinking, oh, there's an important aspect of hearing health care that we're not

565
00:37:43,200 --> 00:37:45,400
tapping into in clinical care.

566
00:37:45,400 --> 00:37:46,400
Let's measure that.

567
00:37:46,400 --> 00:37:47,400
Let's Sherri Smith.

568
00:37:47,400 --> 00:37:52,560
And then it started this whole series of ideas that we've had for how to improve measurements

569
00:37:52,560 --> 00:37:55,000
in hearing health care.

570
00:37:55,000 --> 00:37:56,000
That is so awesome.

571
00:37:56,000 --> 00:37:58,280
Teresa, thank you so much.

572
00:37:58,280 --> 00:37:59,280
That's been gold.

573
00:37:59,280 --> 00:38:02,600
I've learned new things and I feel like you've been teaching me a lot already.

574
00:38:02,600 --> 00:38:04,160
So that was really awesome.

575
00:38:04,160 --> 00:38:05,820
Thank you for being on the show.

576
00:38:05,820 --> 00:38:06,820
It's my pleasure.

577
00:38:06,820 --> 00:38:08,320
Thank you for having me.

578
00:38:08,320 --> 00:38:09,320
All right, everyone.

579
00:38:09,320 --> 00:38:10,320
You've heard Teresa.

580
00:38:10,320 --> 00:38:15,200
There is a lot to think about when it comes to measuring health.

581
00:38:15,200 --> 00:38:19,680
And as you're designing your clinical studies, you want to make sure that what you're measuring

582
00:38:19,680 --> 00:38:24,240
with whatever outcome measure you're using is actually what you want to measure.

583
00:38:24,240 --> 00:38:28,960
And there is no better person to talk to about it than actually a health measurement expert,

584
00:38:28,960 --> 00:38:30,260
the health measurement expert.

585
00:38:30,260 --> 00:38:36,040
So definitely reach out to someone at your institution and look for ways to collaborate

586
00:38:36,040 --> 00:38:39,880
because collaborations with these experts is awesome.

587
00:38:39,880 --> 00:38:40,880
Okay.

588
00:38:40,880 --> 00:38:42,800
It has been a pleasure to talk with you today.

589
00:38:42,800 --> 00:38:45,800
I look forward to talking with you again the next time.

590
00:38:45,800 --> 00:38:46,800
Bye-bye.

591
00:38:46,800 --> 00:38:58,600
Thanks for listening to this episode of the Clinician Researcher Podcast, where academic

592
00:38:58,600 --> 00:39:03,840
clinicians learn the skills to build their own research program, whether or not they

593
00:39:03,840 --> 00:39:05,400
have a mentor.

594
00:39:05,400 --> 00:39:11,520
If you found the information in this episode to be helpful, don't keep it all to yourself.

595
00:39:11,520 --> 00:39:13,240
Someone else needs to hear it.

596
00:39:13,240 --> 00:39:17,300
So take a minute right now and share it.

597
00:39:17,300 --> 00:39:22,760
As you share this episode, you become part of our mission to help launch a new generation

598
00:39:22,760 --> 00:39:35,640
of clinician researchers who make transformative discoveries that change the way we do healthcare.

