Public reporting of clinical trial findings as an ethical responsibility to participants: a qualitative study

Objective To understand how the experiences and views of trial participants, trial investigators and others connected to clinical trial research relate to whether researchers have a duty to participants to publicly report research findings. Design Qualitative interview study. Setting Semistructured interviews held in person or by telephone between March 2019 and April 2021 with participants in the Canadian provinces of Alberta, British Columbia and Ontario. Participants 34 participants, including 10 clinical trial participants, 17 clinical trial investigators, 1 clinical research coordinator, 3 research administrators and 3 research ethics board members. Analysis We conducted a thematic analysis, including qualitative coding of interview transcripts and identification of key themes. Main outcome measures Key themes identified through qualitative coding of interview data. Results Most clinical trial participants felt that reporting clinical trial results is important. Accounts of trial participants suggest their contributions are part of a reciprocal relationship involving the expectation that research will advance medical knowledge. Similarly, comments from trial investigators suggest that reporting trial results is part of reciprocity with trial participants and is a necessary part of honouring informed consent. Accounts of trial investigators suggest that when drug trials are not reported, this may undermine informed consent in subsequent trials by withholding information on harms or efficacy relevant to informed decisions on whether to conduct or enroll in future trials of similar drugs. Conclusion The views of trial participants, trial investigators and others connected to clinical trial research in Canada suggest that researchers have an obligation to participants to publicly report clinical trial results and that reporting results is necessary for honouring informed consent.

Automated summary

Based on interviews with individuals involved in clinical trial research in Canada, including trial participants and investigators, it was found that most participants and investigators believe that publicly reporting trial results is crucial. This relates to the reciprocal relationship between participants and investigators and the fulfillment of informed consent. Failure to report trial results may undermine informed consent and have negative effects on future clinical trial decisions for similar drugs.