Literature DB >> 12150500

Quantitative impact of including consumers in the scientific review of breast cancer research proposals.

Yvonne Andejeski1, Isabelle T Bisceglio, Kay Dickersin, Jean E Johnson, Sabina I Robinson, Helene S Smith, Frances M Visco, Irene M Rich.   

Abstract

OBJECTIVE: To evaluate the impact of having breast cancer survivors with advocacy experience (consumers) participate as voting members of scientific review panels for proposals on breast cancer research. As major stakeholders, patients and other consumer advocates sought inclusion in all decision-making processes affecting funding of disease-targeted research.
METHOD: Cross-sectional analysis of assigned proposal scores ranging from 5.0 (acceptable) to 1.0 (outstanding); before (prepanel) and after (postpanel) opinion questionnaires. Forty-six panels reviewed 2206 proposals for the Fiscal Year 1995 Department of Defense (DOD) Breast Cancer Research Program. Analyses were limited to the 42 panels scheduled to meet on site and the 2190 proposals scored by both participant groups. There were 85 consumers and 638 scientists. The main outcome measures were proposal merit scores (raw, overall, and participant-specific means) and opinions concerning perceived benefits and drawbacks of consumer involvement.
RESULTS: In general, the voting patterns of consumers were similar to those of scientists. Final proposal scores were the same as those that would have been obtained without consumer voting for 76.2% of the proposals, more favorable for 15.2% of the proposals, and less favorable for 8.6% of the proposals. For all but 13 proposals, the difference was +/-0.1. Prepanel opinions regarding consumer involvement were generally positive. Prepanel and postpanel comparisons almost always showed that significantly greater proportions of participants had positive postpanel opinions than had negative postpanel opinions. Having consumers on review panels was reported to be beneficial (83.9% and 98.2% for scientists and consumers, respectively) and to not have drawbacks (74.7% and 87.3%, respectively).
CONCLUSIONS: Our results support continued participation of consumers in our peer review process. The DOD program can serve as a model for other research programs considering consumer involvement.

Entities:  

Mesh:

Year:  2002        PMID: 12150500     DOI: 10.1089/152460902317586010

Source DB:  PubMed          Journal:  J Womens Health Gend Based Med        ISSN: 1524-6094


  22 in total

1.  Redressing past wrongs: changing the common rule to increase minority voices in research.

Authors:  William C Rencher; Leslie E Wolf
Journal:  Am J Public Health       Date:  2013-10-17       Impact factor: 9.308

2.  Can the impact of public involvement on research be evaluated? A mixed methods study.

Authors:  Rosemary Barber; Jonathan D Boote; Glenys D Parry; Cindy L Cooper; Philippa Yeeles; Sarah Cook
Journal:  Health Expect       Date:  2011-02-17       Impact factor: 3.377

Review 3.  Mapping the impact of patient and public involvement on health and social care research: a systematic review.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Health Expect       Date:  2012-07-19       Impact factor: 3.377

Review 4.  Promoting Scientist-Advocate Collaborations in Cancer Research: Why and How.

Authors:  Jeannine M Salamone; Wanda Lucas; Shelley B Brundage; Jamie N Holloway; Sherri M Stahl; Nora E Carbine; Margery London; Naomi Greenwood; Rosa Goyes; Deborah Charles Chisholm; Erin Price; Roberta Carlin; Susan Winarsky; Kirsten B Baker; Julia Maues; Ayesha N Shajahan-Haq
Journal:  Cancer Res       Date:  2018-08-17       Impact factor: 12.701

5.  Supporting cancer survivors' participation in peer review: perspectives from NCI's CARRA program.

Authors:  Melissa B Gilkey
Journal:  J Cancer Surviv       Date:  2013-11-09       Impact factor: 4.442

6.  Involving consumers successfully in NHS research: a national survey.

Authors:  Rosemary Barber; Jonathan D Boote; Cindy L Cooper
Journal:  Health Expect       Date:  2007-12       Impact factor: 3.377

7.  Training of patient and consumer representatives in the basic competencies of evidence-based medicine: a feasibility study.

Authors:  Bettina Berger; Anke Steckelberg; Gabriele Meyer; Jürgen Kasper; Ingrid Mühlhauser
Journal:  BMC Med Educ       Date:  2010-02-11       Impact factor: 2.463

Review 8.  Self-advocacy and cancer: a concept analysis.

Authors:  Teresa L Hagan; Heidi S Donovan
Journal:  J Adv Nurs       Date:  2013-01-24       Impact factor: 3.187

Review 9.  A systematic review of the impact of patient and public involvement on service users, researchers and communities.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Patient       Date:  2014       Impact factor: 3.883

10.  Service user involvement in cancer care: the impact on service users.

Authors:  Phil Cotterell; Gwen Harlow; Carolyn Morris; Peter Beresford; Bec Hanley; Anita Sargeant; John Sitzia; Kristina Staley
Journal:  Health Expect       Date:  2010-10-28       Impact factor: 3.377

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