ArticleContemporary clinical trials communications2016
Exit interviews administered to patients participating in the COSTOP placebo controlled randomised trial in Uganda.
Article in Contemporary clinical trials communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Trial
- How the EMERGE guideline on medication adherence can improve the quality of clinical trials.British journal of clinical pharmacology · 2020Review
- Analysis of Clinical Trial Exit Interview Data in Patients with Treatment-Resistant Depression.The patient · 2019Article
- Using biomarkers to predict TB treatment duration (Predict TB): a prospective, randomized, noninferiority, treatment shortening clinical trial.Gates open research · 2017Article
- Reasons for participating in a randomised clinical trial: The volunteers' voices in the COSTOP trial in Uganda.Contemporary clinical trials communications · 2017Article
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Authors and funding
9 authors.
Funding
Abstract
introductionCOSTOP was a randomised controlled trial designed to assess the risks and benefits to HIV-infected participants stabilised on anti-retroviral treatment of stopping cotrimoxazole (CTX). In order to assess the extent to which patients may have had access to and used CTX other than that supplied as study drug it was decided to conduct an exit interview.
methodsA structured interview was administered by interviewers who were not associated with the COSTOP trial team in order to make it easier for participants to respond truthfully to sensitive questions about adherence to the study protocol.
resultsA total of 1993 participants were interviewed. Only 29 (1.7%) said they had taken their left over CTX; 101 (6.1%) had kept supplies at home. When asked about obtaining open label CTX during the trial 92 (4.7%) participants said they had done so, in contrast to only 12 who admitted doing so when asked at trial visits. The questions participants found most difficult to answer honestly at clinic visits were those concerning adherence to trial drugs (15.6% of participants) and whether they had slept under the insecticide treated mosquito nets (14.9%). DISCUSSION: The exit interview demonstrated that there was some evidence of open label drug being taken by the participants. However, the results from the interview do not suggest that the trial results would have been seriously compromised. We would recommend the exit interview as a valuable way of assessing adherence to trial procedures.
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