Literature DB >> 17063137

Measuring trust in medical researchers.

Mark A Hall1, Fabian Camacho, Janice S Lawlor, Venita Depuy, Jeremy Sugarman, Kevin Weinfurt.   

Abstract

BACKGROUND: Concern is widespread that the public's and participants' trust in medical research is threatened, but few empirical measures of research trust exist. This project aims to enable more rigorous study of researcher trust by developing and testing appropriate survey measures.
METHODS: Survey items were developed based on a conceptual model of the primary domains of researcher trust (safety, fidelity, honesty, global trust). Pilot testing was conducted on a regional convenience sample of adults (n = 124). Exploratory factor analyses of the data were performed, and an item selection procedure reduced the number of survey questions. A final set of 12 items was validated, and a 4-item short version of the researcher trust scale was selected and tested in a national web-based survey of asthma and diabetes patients (n = 3623). Further factor analysis and validation were performed on this larger sample.
RESULTS: Both the full and short scales have a single-factor structure with acceptable internal reliability (alphas of 0.87 [12 items] and 0.72 [4 items]). Trust in physician researchers and trust in medical researchers generally were found not to be separate constructs. In the national sample, the short scale was positively associated with better health status, prior participation in medical research, and willingness to participate in a hypothetical medical research study, and negatively associated with African-American race and higher education.
CONCLUSIONS: Trust in medical researchers is a measurable single-factor construct including trust in safety, researcher fidelity, and honesty. This new scale provides an empirical tool for informing the ethics and public policy of medical research.

Entities:  

Mesh:

Year:  2006        PMID: 17063137     DOI: 10.1097/01.mlr.0000228023.37087.cb

Source DB:  PubMed          Journal:  Med Care        ISSN: 0025-7079            Impact factor:   2.983


  60 in total

1.  Differences in the patterns of health care system distrust between blacks and whites.

Authors:  Katrina Armstrong; Suzanne McMurphy; Lorraine T Dean; Ellyn Micco; Mary Putt; Chanita Hughes Halbert; J Sanford Schwartz; Pamela Sankar; Reed E Pyeritz; Barbara Bernhardt; Judy A Shea
Journal:  J Gen Intern Med       Date:  2008-02-26       Impact factor: 5.128

2.  Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.

Authors:  Saskia C Sanderson; Kyle B Brothers; Nathaniel D Mercaldo; Ellen Wright Clayton; Armand H Matheny Antommaria; Sharon A Aufox; Murray H Brilliant; Diego Campos; David S Carrell; John Connolly; Pat Conway; Stephanie M Fullerton; Nanibaa' A Garrison; Carol R Horowitz; Gail P Jarvik; David Kaufman; Terrie E Kitchner; Rongling Li; Evette J Ludman; Catherine A McCarty; Jennifer B McCormick; Valerie D McManus; Melanie F Myers; Aaron Scrol; Janet L Williams; Martha J Shrubsole; Jonathan S Schildcrout; Maureen E Smith; Ingrid A Holm
Journal:  Am J Hum Genet       Date:  2017-02-09       Impact factor: 11.025

3.  Development of a revised Health Care System Distrust scale.

Authors:  Judy A Shea; Ellyn Micco; Lorraine T Dean; Suzanne McMurphy; J Sanford Schwartz; Katrina Armstrong
Journal:  J Gen Intern Med       Date:  2008-03-28       Impact factor: 5.128

4.  Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.

Authors:  J M Oliver; M J Slashinski; T Wang; P A Kelly; S G Hilsenbeck; A L McGuire
Journal:  Public Health Genomics       Date:  2011-12-30       Impact factor: 2.000

5.  A paradigm for understanding trust and mistrust in medical research: The Community VOICES study.

Authors:  M Smirnoff; I Wilets; D F Ragin; R Adams; J Holohan; R Rhodes; G Winkel; E M Ricci; C Clesca; L D Richardson
Journal:  AJOB Empir Bioeth       Date:  2018-02-16

6.  Improving informed consent: Stakeholder views.

Authors:  Emily E Anderson; Susan B Newman; Alicia K Matthews
Journal:  AJOB Empir Bioeth       Date:  2017-08-02

7.  Broad Consent for Research on Biospecimens: The Views of Actual Donors at Four U.S. Medical Centers.

Authors:  Teddy D Warner; Carol J Weil; Christopher Andry; Howard B Degenholtz; Lisa Parker; Latarsha J Carithers; Michelle Feige; David Wendler; Rebecca D Pentz
Journal:  J Empir Res Hum Res Ethics       Date:  2018-02-01       Impact factor: 1.742

8.  Psychometric Properties of a Decisional Capacity Screening Tool for Individuals Contemplating Participation in Alzheimer's Disease Research.

Authors:  Jennifer Burgher Seaman; Lauren Terhorst; Amanda Gentry; Amanda Hunsaker; Lisa S Parker; Jennifer Hagerty Lingler
Journal:  J Alzheimers Dis       Date:  2015       Impact factor: 4.472

9.  Effects of disclosing financial interests on attitudes toward clinical research.

Authors:  Kevin P Weinfurt; Mark A Hall; Michaela A Dinan; Venita DePuy; Joëlle Y Friedman; Jennifer S Allsbrook; Jeremy Sugarman
Journal:  J Gen Intern Med       Date:  2008-04-02       Impact factor: 5.128

10.  Informed recruitment in partner studies of HIV transmission: an ethical issue in couples research.

Authors:  Louise-Anne McNutt; Elisa J Gordon; Anneli Uusküla
Journal:  BMC Med Ethics       Date:  2009-08-27       Impact factor: 2.652

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