Literature DB >> 29631487

Development and Preliminary Testing of the Perceived Benefit and Burden Scales for Cancer Clinical Trial Participation.

Connie M Ulrich1, Qiuping Pearl Zhou2, Sarah J Ratcliffe1, Kathleen Knafl3, Gwenyth R Wallen4, Therese S Richmond1, Christine Grady4.   

Abstract

We developed measures of benefits and burdens of research participation in cancer clinical trials using a sequential mixed methods design with a qualitative ( n = 32) and quantitative sample ( n = 110) of cancer clinical trial participants. Benefit-burden items (22 for benefits, 23 for burdens) were subsequently developed and assessed through cognitive interviewing for content, clarity, and meaning. Preliminary psychometric analyses support the internal consistency reliability and construct validity of Benefit (α = .90) and Burden (α = .87) research participation scales. Item response theory models supported the discrimination ability of the items on the scales. Participants who had thoughts of dropping out had lower Benefit scale scores ( p < .001) and higher Burden scores ( p < .001) than those who had no thoughts of dropping out, supporting construct validity. With further psychometric testing, the scale can be used to develop appropriate interventions to address recruitment and retention of human participants in clinical research.

Entities:  

Keywords:  cancer; clinical trials; psychological distress; risks and benefits; symptoms

Mesh:

Year:  2018        PMID: 29631487      PMCID: PMC6091872          DOI: 10.1177/1556264618764730

Source DB:  PubMed          Journal:  J Empir Res Hum Res Ethics        ISSN: 1556-2646            Impact factor:   1.742


  10 in total

1.  Racial disparities in Hodgkin's lymphoma: a comprehensive population-based analysis.

Authors:  A M Evens; M Antillón; B Aschebrook-Kilfoy; B C-H Chiu
Journal:  Ann Oncol       Date:  2012-01-11       Impact factor: 32.976

2.  Cognitive interviewing as a tool for improving the informed consent process.

Authors:  Gordon Willis
Journal:  J Empir Res Hum Res Ethics       Date:  2006-03       Impact factor: 1.742

3.  A New Measure of Research Participant Burden: Brief Report.

Authors:  Jennifer H Lingler; Karen L Schmidt; Amanda L Gentry; Lu Hu; Lauren A Terhorst
Journal:  J Empir Res Hum Res Ethics       Date:  2014-10       Impact factor: 1.742

4.  Views of adolescents and parents on pediatric research without the potential for clinical benefit.

Authors:  David Wendler; Emily Abdoler; Lori Wiener; Christine Grady
Journal:  Pediatrics       Date:  2012-09-10       Impact factor: 7.124

5.  Why patients continue to participate in clinical research.

Authors:  David Wendler; Benjamin Krohmal; Ezekiel J Emanuel; Christine Grady
Journal:  Arch Intern Med       Date:  2008-06-23

6.  Developing a Model of the Benefits and Burdens of Research Participation in Cancer Clinical Trials.

Authors:  Connie M Ulrich; Kathleen A Knafl; Sarah J Ratcliffe; Therese S Richmond; Christine Grady; Claiborne Miller-Davis; Gwenyth R Wallen
Journal:  AJOB Prim Res       Date:  2012

7.  Participation in cancer clinical trials: race-, sex-, and age-based disparities.

Authors:  Vivek H Murthy; Harlan M Krumholz; Cary P Gross
Journal:  JAMA       Date:  2004-06-09       Impact factor: 56.272

8.  Racial disparities in cancer survival among randomized clinical trials patients of the Southwest Oncology Group.

Authors:  Kathy S Albain; Joseph M Unger; John J Crowley; Charles A Coltman; Dawn L Hershman
Journal:  J Natl Cancer Inst       Date:  2009-07-07       Impact factor: 13.506

9.  Cancer clinical trial participants' assessment of risk and benefit.

Authors:  Connie M Ulrich; Sarah J Ratcliffe; Gwenyth R Wallen; Qiuping Pearl Zhou; Kathleen Knafl; Christine Grady
Journal:  AJOB Empir Bioeth       Date:  2015-05-01

10.  A Research Agenda for Communication Between Health Care Professionals and Patients Living With Serious Illness.

Authors:  James A Tulsky; Mary Catherine Beach; Phyllis N Butow; Susan E Hickman; Jennifer W Mack; R Sean Morrison; Richard L Street; Rebecca L Sudore; Douglas B White; Kathryn I Pollak
Journal:  JAMA Intern Med       Date:  2017-09-01       Impact factor: 21.873

  10 in total
  3 in total

1.  The Benefits and Burdens of Pediatric Palliative Care and End-of-Life Research: A Systematic Review.

Authors:  Meaghann S Weaver; Kim Mooney-Doyle; Katherine Patterson Kelly; Kathleen Montgomery; Amy R Newman; Christine A Fortney; Cynthia J Bell; Jessica L Spruit; Melissa Kurtz Uveges; Lori Wiener; Cynthia M Schmidt; Vanessa N Madrigal; Pamela S Hinds
Journal:  J Palliat Med       Date:  2019-03-05       Impact factor: 2.947

2.  Key recruitment and retention strategies for a pilot web-based intervention to decrease obesity risk among minority youth.

Authors:  Grisselle DeFrank; Sarina Singh; Katrina F Mateo; Laura Harrison; Alyson Rosenthal; Allison Gorman; May May Leung
Journal:  Pilot Feasibility Stud       Date:  2019-09-05

Review 3.  Key considerations to reduce or address respondent burden in patient-reported outcome (PRO) data collection.

Authors:  Olalekan Lee Aiyegbusi; Jessica Roydhouse; Samantha Cruz Rivera; Paul Kamudoni; Peter Schache; Roger Wilson; Richard Stephens; Melanie Calvert
Journal:  Nat Commun       Date:  2022-10-12       Impact factor: 17.694

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.