Grady, C; Touloumi, G; Walker, AS; Smolskis, M; Sharma, S; Babiker, AG; Pantazis, N; ... START Informed Consent Substudy Group, .; + view all Grady, C; Touloumi, G; Walker, AS; Smolskis, M; Sharma, S; Babiker, AG; Pantazis, N; Tavel, J; Florence, E; Sanchez, A; Hudson, F; Papadopoulos, A; Emanuel, E; Clewett, M; Munroe, D; Denning, E; START Informed Consent Substudy Group, .; - view fewer (2017) A randomized trial comparing concise and standard consent forms in the START trial. PLoS ONE , 12 (4) , Article e0172607. 10.1371/journal.pone.0172607.

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Abstract

BACKGROUND: Improving the effectiveness and efficiency of research informed consent is a high priority. Some express concern about longer, more complex, written consent forms creating barriers to participant understanding. A recent meta-analysis concluded that randomized comparisons were needed. METHODS: We conducted a cluster-randomized non-inferiority comparison of a standard versus concise consent form within a multinational trial studying the timing of starting antiretroviral therapy in HIV+ adults (START). Interested sites were randomized to standard or concise consent forms for all individuals signing START consent. Participants completed a survey measuring comprehension of study information and satisfaction with the consent process. Site personnel reported usual site consent practices. The primary outcome was comprehension of the purpose of randomization (pre-specified 7.5% non-inferiority margin). RESULTS: 77 sites (2429 participants) were randomly allocated to use standard consent and 77 sites (2000 participants) concise consent, for an evaluable cohort of 4229. Site and participant characteristics were similar for the two groups. The concise consent was non-inferior to the standard consent on comprehension of randomization (80.2% versus 82%, site adjusted difference: 0.75% (95% CI -3.8%, +5.2%)); and the two groups did not differ significantly on total comprehension score, satisfaction, or voluntariness (p>0.1). Certain independent factors, such as education, influenced comprehension and satisfaction but not differences between consent groups. CONCLUSIONS: An easier to read, more concise consent form neither hindered nor improved comprehension of study information nor satisfaction with the consent process among a large number of participants. This supports continued efforts to make consent forms more efficient. TRIAL REGISTRATION: Informed consent substudy was registered as part of START study in clinicaltrials.gov #NCT00867048, and EudraCT # 2008-006439-12.

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