collaboratory coordinating center ethics supplement
TRANSCRIPT
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Collaboratory Coordinating Center
Ethics Supplement
Jeremy Sugarman, MD, MPH, MA
Kevin Weinfurt, PhD
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Major Areas of Controversy
•Consent
•Risks and benefits
• Standard of care
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NIH Ethics Supplements
Coordinating Center
(Duke & Hopkins)
TiME(University of Pennsylvania)
ABATE(University of
California - Irvine)
NIH CollaboratoryCTSA(University of Washington &
Stanford)
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Collaboratory Coordinating CenterEthics Supplement Team• PI: Rob Califf
• Project leads: Jeremy Sugarman and Kevin Weinfurt
• Duke• Laura Beskow
• Kate Brelsford
• Travis Crayton
• Johns Hopkins• Juli Bollinger
• Matt DeCamp
• Rachel Dvoskin
• Nancy Kass
• Debra Mathews
• Rachel Topazian
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Overarching Goal
To improve understanding of when and how different stakeholders believe research testing or comparing interventions that are each considered standard of care are acceptable and when traditional or modified approaches to consent for it should be sought.
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Project Aims
AIM 1: Collect rich qualitative data from patients to identify the broad range of attitudes, beliefs, and preferences concerning the need for research in usual care settings and related consent issues.
AIM 2: Systematically identify the factors that influence U.S. adults’ beliefs concerning research and consent in different usual care situations.
AIM 3: Convene a summit meeting to share emerging results and findings from related projects.
AIM 4: Elicit stakeholders’ views concerning the appropriate models of oversight and consent for research on standard health care practices.
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Year
1
IRB Chairs, Nurses, Investigators(6 conducted)
Formative Stakeholder Interviews
Clinician Interviews
(1 of 2 pilots conducted)Patient Focus
Groups(10 conducted)
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Year
2Patient Quantitative
Survey
Additional Stakeholder Interviews
• Include policy makers• Ask participants to consider policy
regarding oversight and consent in light of findings
Additional Patient Focus
Groups/Interviews
• Discuss the information patients desire concerning various learning activities
We will convene a summit meeting in consultation with NIH (date TBD)
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CER Focus Groups
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Patient Focus Groups (n = 14)
•Population: general public
• Location
•Durham, NC
•Baltimore, MD
•Washington, DC
•Chicago, IL (planned)
• San Francisco, CA (planned)
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Patient Focus Groups: Types & Domains
• Two types of groups:
1. Comparative Effectiveness
2. Medical Center Operations & Clinician Education/Support
• Acceptability of four methods of notification/consent:
• General notification
• Oral
• Oral + information sheet
• Express written consent
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4 Preliminary Observations
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1. Acceptability of “equipoise” in the abstract vs my doctor’s uncertainty
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I’m not a 100 percent confident that my doctor's decision is always better than chance. What I am confident in, is if we flip that question, that my doctor's decision will never be worse than a selection by chance.”
But if a doctor said, ‘I really don’t know which one would be better for you,’ I’d look at him and think, I'm gonna find me another doctor. Because you're supposed to know.
. . . but I just would prefer the doctor’s opinion and expertise versus just the computer just closing its eyes and saying, “Here, take one.”
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2. Strong associations with “traditional” research interferes with understanding of CER
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3. Some nuanced appreciation of tradeoffs associated with different notification/consent models
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Well I would be [leery of a multi-page consent form]. Because if it is something that is simple, why would it take ten pages to describe it as opposed to the amount of space that is taken up here?
I don't want to participate in a study to sign my life away but [. . . ] maybe a page or two that this is what this study is, are you good with it? Check yes or no.
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4. What does signing a consent document mean to people?
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[By] signing here, it's like, I know everything that's going on. You have told me everything that is going on. So if something goes wrong, someone is taking responsibility.
To me I feel like because I'm gonna sign it, I grasp it better. I put more energy into knowing what's what. [The] risks and benefits.
And that also protects the institution, that there is documented paperwork that I opted into it. As opposed to, “Oh, he told us verbally,” which isn't actually provable in the future.
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What would you like to ask the U.S. adult population about all of this?
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Q & A