Literature DB >> 16713523

A brief measure of perceived understanding of informed consent in a clinical trial was validated.

Peter Guarino1, Donna L Lamping, Diana Elbourne, James Carpenter, Peter Peduzzi.   

Abstract

BACKGROUND AND
OBJECTIVE: To develop and evaluate an Informed Consent Questionnaire (ICQ) for measuring self-reported perceived understanding of informed consent in a randomized clinical trial.
METHODS: The study was embedded in a Department of Veterans Affairs randomized clinical trial of Gulf War veterans' illnesses (CSP#470). The trial was initiated in May 1999 at 20 hospitals and concluded in September 2001; 1,092 participants were enrolled and followed for 12 months. The reliability and validity sample included 1,086 participants evaluated at baseline, 906 at 3 months, 929 at 6 months, and 910 at 12 months. The psychometric evaluations included tests of acceptability (based on missing data, endorsement frequencies, and floor/ceiling effects), item reduction, internal consistency, and construct validity (based on Cronbach's alpha coefficients, item-total correlations, and principal components analysis).
RESULTS: The ICQ had >5% missing information on some questions at baseline, indicating poor acceptability prior to the initiation of the trial; however, the scale had good acceptability at each of the follow-up visits. Psychometric evaluation following standard item reduction techniques confirmed the reliability and validity of a four-item subscale of the ICQ (ICQ-4).
CONCLUSIONS: The ICQ-4 is a simple and psychometrically sound self-report measure of perceived understanding of informed consent.

Entities:  

Mesh:

Year:  2006        PMID: 16713523     DOI: 10.1016/j.jclinepi.2005.11.009

Source DB:  PubMed          Journal:  J Clin Epidemiol        ISSN: 0895-4356            Impact factor:   6.437


  11 in total

1.  Measuring the process and quality of informed consent for clinical research: development and testing.

Authors:  Elizabeth Gross Cohn; Haomiao Jia; Winifred Chapman Smith; Katherine Erwin; Elaine L Larson
Journal:  Oncol Nurs Forum       Date:  2011-07       Impact factor: 2.172

2.  Time to Improve Informed Consent for Dialysis: An International Perspective.

Authors:  Frank Brennan; Cameron Stewart; Hannah Burgess; Sara N Davison; Alvin H Moss; Fliss E M Murtagh; Michael Germain; Shelley Tranter; Mark Brown
Journal:  Clin J Am Soc Nephrol       Date:  2017-04-04       Impact factor: 8.237

3.  Sex differences in the incidence of peripheral neuropathy among Kenyans initiating antiretroviral therapy.

Authors:  Sapna A Mehta; Aabid Ahmed; Maura Laverty; Robert S Holzman; Fred Valentine; Sumathi Sivapalasingam
Journal:  Clin Infect Dis       Date:  2011-09       Impact factor: 9.079

Review 4.  Participants' understanding of informed consent in clinical trials over three decades: systematic review and meta-analysis.

Authors:  Nguyen Thanh Tam; Nguyen Tien Huy; Le Thi Bich Thoa; Nguyen Phuoc Long; Nguyen Thi Huyen Trang; Kenji Hirayama; Juntra Karbwang
Journal:  Bull World Health Organ       Date:  2015-01-22       Impact factor: 9.408

5.  Informed consent in randomised controlled trials: development and preliminary evaluation of a measure of Participatory and Informed Consent (PIC).

Authors:  Julia Wade; Daisy Elliott; Kerry N L Avery; Daisy Gaunt; Grace J Young; Rebecca Barnes; Sangeetha Paramasivan; W Bruce Campbell; Jane M Blazeby; Alison J Birtle; Rob C Stein; David J Beard; Alison W Halliday; Jenny L Donovan
Journal:  Trials       Date:  2017-07-17       Impact factor: 2.279

6.  Measuring informed consent capacity in an Alzheimer's disease clinical trial.

Authors:  Peter D Guarino; Julia E Vertrees; Sanjay Asthana; Mary Sano; Maria D Llorente; Muralidhar Pallaki; Susan Love; Gerard D Schellenberg; Maurice W Dysken
Journal:  Alzheimers Dement (N Y)       Date:  2016-09-20

7.  Patients' perception of quality of pre-operative informed consent in athens, Greece: a pilot study.

Authors:  Matthew E Falagas; Patrick D Akrivos; Vangelis G Alexiou; Vasilios Saridakis; Theofanis Moutos; George Peppas; Barbara K Kondilis
Journal:  PLoS One       Date:  2009-11-26       Impact factor: 3.240

8.  Digitised audio questionnaire for assessment of informed consent comprehension in a low-literacy African research population: development and psychometric evaluation.

Authors:  Muhammed O Afolabi; Kalifa Bojang; Umberto D'Alessandro; Martin O C Ota; Egeruan B Imoukhuede; Raffaella Ravinetto; Heidi J Larson; Nuala McGrath; Daniel Chandramohan
Journal:  BMJ Open       Date:  2014-06-24       Impact factor: 2.692

9.  Making a decision about trial participation: the feasibility of measuring deliberation during the informed consent process for clinical trials.

Authors:  Katie Gillies; Glyn Elwyn; Jonathan Cook
Journal:  Trials       Date:  2014-07-30       Impact factor: 2.279

10.  Patient information leaflets (PILs) for UK randomised controlled trials: a feasibility study exploring whether they contain information to support decision making about trial participation.

Authors:  Katie Gillies; Wan Huang; Zoë Skea; Jamie Brehaut; Seonaidh Cotton
Journal:  Trials       Date:  2014-02-18       Impact factor: 2.279

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