Voluntariness of consent to HIV clinical research: A conceptual and empirical pilot study.

Abstract:

:Obtaining voluntary informed consent for research participation is an ethical imperative, yet there appears to be little consensus regarding what constitutes a voluntary consent decision. An instrument to assess influences on participants' consent decision and perceived voluntariness was developed and piloted in two South African HIV clinical trials. The pilot study found high levels of perceived voluntariness. The feeling of having no choice but to participate was significantly associated with lower perceived voluntariness. Overall the data suggest that it is possible to obtain voluntary and valid consent for research participants in ethically complex HIV clinical trials in a developing country context.

journal_name

J Health Psychol

authors

Mamotte N,Wassenaar D

doi

10.1177/1359105316628737

subject

Has Abstract

pub_date

2017-09-01 00:00:00

pages

1387-1404

issue

11

eissn

1359-1053

issn

1461-7277

pii

1359105316628737

journal_volume

22

pub_type

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