Theoretically-informed vs standard cover letter to improve participant response to mailed questionnaire: results of an embedded randomised retention trial.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-11-14 DOI:10.1186/s13063-024-08565-0
Colin C Everett, Sarah T Brown, Joanna L Dennett, Howard Collier, Claire L Davies, Frances Game, E Andrea Nelson
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引用次数: 0

Abstract

Background: Participant non-response is a source of bias in all research, especially in randomised controlled trials. Participants followed up remotely can have high non-response rates. Four such trials have been conducted of a cover letter with content informed by behaviour change theory to overcome hypothesised barriers to responding to a mailed questionnaire. Pooled results to date have suggested further research to be worthwhile. We conducted an embedded randomised study within a trial of such cover letters in the hope that we would improve response rates to our postal quality of life questionnaires.

Methods: One hundred forty-eight participants in the CODIFI2 diabetic foot ulcer sampling trial were randomised 1:1 to receive one of two different cover letters at follow-up timepoints: either a standard cover letter accompanying their postal follow-up questionnaires or to an 'enhanced' (theory-informed) cover letter. Questionnaires were mailed at 39, 52 and (for some participants) 104 weeks post randomisation. Outcome measures were response to mailing at each timepoint. Analysis was restricted to those for whom a questionnaire and letter was issued. Owing to limited recruitment, a reduced analysis plan, comprising solely observed response rates and 95% confidence intervals for difference in response rates was followed. Post hoc, we added our week 52 results to an already-published meta-analysis.

Results: Sixty-seven out of 74 enhanced cover letter group (Enhanced) and 67/74 standard cover letter group (Standard) participants who had not already died or withdrawn were sent their first mailing at 39 weeks. The 39-week response rates were 47/67 (70.1%) and 39/67 (58.2%) for Enhanced and Standard participants, respectively. At week 52, the response rates were 45/64 (70.3%) and 35/63 (55.6%) for Enhanced and Standard participants, respectively. At week 104, the response rates were 24/33 (72.7%) and 19/33 (57.6%) for the Enhanced and Standard participants, respectively. Adding our week 52 results to a published meta-analysis increased the pooled estimate of differences in response rates to 0.04 (- 0.01 to 0.09) favouring enhanced letters.

Conclusion: While this embedded randomised controlled trial observed greater response rates at all times among those randomised to the enhanced letter, the reduced sample size meant that these results are imprecise.

Trial registration: ISRCTN registry ISRCTN74929588. Registered on 5 March 2019.

以理论为依据的封面信函与标准封面信函相比,如何提高受试者对邮寄问卷的回复率:嵌入式随机保留试验的结果。
背景:在所有研究中,尤其是在随机对照试验中,参试者不回复是造成偏差的一个原因。远程跟踪的参与者可能会有很高的无回复率。目前已经进行了四项此类试验,试验内容是根据行为改变理论编写的一封求职信,以克服邮寄问卷的假设障碍。迄今为止的汇总结果表明值得进一步研究。我们在此类封面信的试验中进行了一项嵌入式随机研究,希望能提高邮寄生活质量问卷的回复率:CODIFI2 糖尿病足溃疡抽样试验的 148 名参与者按 1:1 随机分配,在随访时间点收到两种不同封面信函中的一种:一种是随邮寄随访问卷附送的标准封面信函,另一种是 "增强型"(理论依据型)封面信函。问卷分别在随机分组后 39 周、52 周和(部分参与者)104 周邮寄。结果测量指标为每个时间点的邮寄回复率。分析仅限于收到问卷和信件的参与者。由于招募人数有限,我们采用了一个简化的分析计划,其中只包括观察到的回复率和回复率差异的 95% 置信区间。事后,我们将第 52 周的结果加入到已发表的荟萃分析中:在 74 位增强型封面信函组(增强型)和 67/74 位标准型封面信函组(标准型)参与者中,有 67 位尚未死亡或退出,他们在 39 周时收到了第一封邮件。强化组和标准组在 39 周的回复率分别为 47/67(70.1%)和 39/67(58.2%)。在第 52 周,"加强版 "和 "标准版 "参与者的回复率分别为 45/64(70.3%)和 35/63(55.6%)。在第 104 周,增强型和标准型参与者的应答率分别为 24/33 (72.7%)和 19/33 (57.6%)。将我们第 52 周的结果加入到已发表的荟萃分析中,可将应答率差异的集合估计值提高到 0.04(- 0.01 至 0.09),更倾向于增强型信件:尽管这项嵌入式随机对照试验观察到,随机接受增强型信件治疗的患者在所有时间的应答率都更高,但样本量的减少意味着这些结果并不精确:ISRCTN注册号:ISRCTN74929588。注册日期:2019 年 3 月 5 日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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