Long-term follow-up of clinical trial participants: Predictors of post-trial response in older subjects

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Sarah T. Stahl , Emilee Croswell , Khusbu Patel , Ioana Neagoe , Sejuty Minhaj , Ada Lopaczynski , Thandi Lyew
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Abstract

Background and objective

The post-trial follow-up (PTFU) phase of a clinical trial can provide important information on maintenance of intervention effects. However, approaches for the PTFU are rarely described. This short communication describes our process for PTFU that involved recontacting older subjects who participated in a clinical trial between 2015 and 2019. We also describe correlates of response to our PTFU survey.

Methods

The parent clinical trial aimed to reduce depression symptoms among older spousally-bereaved adults. We attempted to recontact our sample during the early stages of the COVID-19 pandemic. Using logistic regression, we examined physical health, depression symptoms, cognitive status, and disability as correlates of participant response to the PTFU phase.

Results

Forty-two percent of participants responded to the PTFU survey. Disability – or the inability to participate in major life tasks and social roles - was significantly associated with response. Participants with greater disability were less likely to respond to the PTFU survey.

Conclusions

Older adults with disabilities may need alternative and supportive strategies for engaging in the PTFU phase.

Clinical Trials Registration: NCT02631291

临床试验参与者的长期随访:老年受试者试验后反应的预测因素
背景和目的:临床试验的试验后随访(PTFU)阶段可以提供有关干预效果维持情况的重要信息。然而,有关 PTFU 的方法却鲜有描述。本短文介绍了我们的 PTFU 流程,该流程涉及重新联系 2015 年至 2019 年期间参与临床试验的老年受试者。我们还描述了PTFU调查响应的相关性:父母临床试验旨在减轻失去配偶的老年人的抑郁症状。我们试图在 COVID-19 大流行的早期阶段重新联系我们的样本。通过逻辑回归法,我们研究了身体健康、抑郁症状、认知状况和残疾程度与参与者对 PTFU 阶段反应的相关性:42%的参与者回复了 PTFU 调查。残疾--即无法参与主要生活任务和社会角色--与回复率有显著关联。残疾程度越严重的参与者越不可能回复 PTFU 调查:结论:残疾老年人可能需要其他支持性策略来参与 PTFU 阶段:临床试验注册:NCT02631291。
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
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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