Evidence map›Paper›PMID 38192107›Full record

ArticleJournal of empirical research on human research ethics : JERHRE2024

"My Blood, You Know, My Biology Being out There…": Consent and Participant Control of Biological Samples.

Susan Racine Passmore, Abigail Gerbitz, Gregory R Hancock, Laura Evans, Gina Green-Harris, Dorothy Farrar Edwards, Tyson Jackson, Stephen B Thomas

Abstract read
In one paragraph

Article in Journal of empirical research on human research ethics : JERHRE, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Susan Racine PassmoreSchool of Nursing, University of Wisconsin, Madison, WI, USA.ORCID 0000-0003-1080-2392
Abigail GerbitzSchool of Nursing, University of Wisconsin, Madison, WI, USA.
Gregory R HancockDepartment of Human Development and Quantitative Methodology, College of Education, University of Maryland, College Park, MD, USA.
Laura EvansHuman Development and Family Studies, School of Human Ecology, University of Wisconsin, Madison, WI, USA.ORCID 0000-0002-0302-8952
Gina Green-HarrisCenter for Community Engagement and Health Partnerships, School of Medicine and Public Health, University of Wisconsin, Madison, WI, USA.
Dorothy Farrar EdwardsSchool of Nursing, University of Wisconsin, Madison, WI, USA.
Tyson JacksonSchool of Nursing, University of Wisconsin, Madison, WI, USA.
Stephen B ThomasCenter for Health Equity, School of Public Health, University of Maryland, College Park, MD, USA.
University of Wisconsin–Madison · USUniversity of Maryland, College Park · US

Funding

University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9M
Wisconsin Alzheimer's Disease Research CenterP30AG062715 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI Sanjay Asthana · 2019 to 2026
$34.5M
Feasibility of an Innovative Method to Understand the Dynamics of Choice and Create Diversity in Genomics Research among Older African AmericansR21HG011503 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI PASSMORE, SUSAN RACINE · 2020 to 2021
$363k
NCATS NIH HHS UL1 TR002373NHGRI NIH HHS R21 HG011503NIA NIH HHS P30 AG062715
6 · The paper itself

Abstract

The widespread and persistent underrepresentation of groups experiencing health disparities in research involving biospecimens is a barrier to scientific knowledge and advances in health equity. To ensure that all groups have the opportunity to participate in research and feel welcome and safe doing so, we must understand how research studies may be shaped to promote inclusion. In this study, we explored the decision to participate in hypothetical research scenarios among African American adults (n = 169) that varied on the basis of four attributes (form of consent, reason for research, institutional affiliation and race of the researcher). Findings indicate that participants were largely willing to contribute to biobanks but significantly preferred opportunities where they had control over the use of their biological samples through tiered or study-specific forms of consent. Broad consent procedures, although common and perhaps preferred by participants with high trust in researchers, may amount to an exclusionary practice.

Indexed as

Biomedical ResearchAdultBiological Specimen BanksBiologyHealth FacilitiesHumansInformed ConsentAfrican Americanbiospecimensgenomicshealth equityInclusive research practicesresearch participation

Identifiers

PMID38192107
PMCPMC10957312
OpenAlexW4390726848

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.