Influences on clinical trial participation: Enhancing recruitment through a gender lens - A scoping review

IF 1.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Lyndon J. Hawke , Elizabeth Nelson , Penny O'Brien , Kay M. Crossley , Peter F. Choong , Samantha Bunzli , Michelle M. Dowsey
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引用次数: 0

Abstract

Background

Suboptimal clinical trial recruitment contributes to research waste. Evidence suggests there may be gender-based differences in willingness to participate in clinical research. Identifying gender-based differences impacting the willingness of trial participation may assist trial recruitment.

Objectives

To examine factors that influence the willingness of men and women to participate in clinical trials and to identify modifiable factors that may be targeted to optimise trial participation.

Material and methods

Electronic databases were searched with key words relating to ‘gender’, ‘willingness to participate’ and ‘trial’. Included studies were English language and reported gender-based differences in willingness to participate in clinical trials, or factors that influence a single gender to participate in clinical trials. Studies were excluded if they described the demographic factors of trial participants or if the majority of participants were pregnant. Extracted data were coded, categorized, analysed thematically and interpreted using Arksey and O'Malley's framework.

Results

Sixty-three studies were included. Two main themes were identified: trial characteristics and participant characteristics. A number of gender-based differences moderating willingness to participate were observed although only one, ‘concern for self’ was found to influence actual trial participation rates between genders.

Conclusion

The relationship between factors influencing willingness to participate in clinical trials is complex. The influence of gender on willingness to participate, while important, may be moderated by other factors including socioeconomic status, ethnicity and health condition. Exploring factors that influence willingness to participate specific to a study cohort likely offers the most promise to optimise trial recruitment of that cohort.

临床试验参与的影响因素:通过性别视角加强招募--范围审查
背景不理想的临床试验招募造成了研究浪费。有证据表明,参与临床研究的意愿可能存在性别差异。材料与方法使用 "性别"、"参与意愿 "和 "试验 "等关键词对电子数据库进行检索。所纳入的研究均为英文研究,并报告了参与临床试验意愿的性别差异或影响单一性别参与临床试验的因素。如果研究描述了试验参与者的人口统计学因素,或大多数参与者为孕妇,则排除在外。采用 Arksey 和 O'Malley 的框架对提取的数据进行编码、分类、专题分析和解释。确定了两大主题:试验特征和参与者特征。尽管只有 "对自我的关注 "这一项被发现会影响不同性别的实际试验参与率,但还是观察到了一些基于性别的差异对参与意愿的调节作用。性别对参与意愿的影响虽然重要,但可能会被其他因素(包括社会经济地位、种族和健康状况)所调节。探索影响研究人群参与意愿的特定因素可能最有希望优化该人群的试验招募。
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来源期刊
Contemporary Clinical Trials Communications
Contemporary Clinical Trials Communications Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
2.70
自引率
6.70%
发文量
146
审稿时长
20 weeks
期刊介绍: Contemporary Clinical Trials Communications is an international peer reviewed open access journal that publishes articles 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 a wide range of disciplines including medicine, life science, pharmaceutical science, biostatistics, epidemiology, computer science, management science, behavioral science, and bioethics. Contemporary Clinical Trials Communications is unique in that it is outside the confines of disease specifications, and it strives to increase the transparency of medical research and reduce publication bias by publishing scientifically valid original research findings irrespective of their perceived importance, significance or impact. Both randomized and non-randomized trials are within the scope of the Journal. Some common topics include trial design rationale and methods, operational methodologies and challenges, and positive and negative trial results. In addition to original research, the Journal also welcomes other types of communications including, but are not limited to, methodology reviews, perspectives and discussions. Through timely dissemination of advances in clinical trials, the goal of Contemporary Clinical Trials Communications is to serve as a platform to enhance the communication and collaboration within the global clinical trials community that ultimately advances this field of research for the benefit of patients.
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