Health Services Research Unit, University of Aberdeen, Aberdeen, UK.
School of Nursing, Midwifery and Health, Coventry University, Coventry, England.
Syst Rev. 2020 Sep 29;9(1):224. doi: 10.1186/s13643-020-01471-x.
Retention of participants is essential to ensure the statistical power and internal validity of clinical trials. Poor participant retention reduces power and can bias the estimates of intervention effect. There is sparse evidence from randomised comparisons of effective strategies to retain participants in randomised trials. Currently, non-randomised evaluations of trial retention interventions embedded in host clinical trials are rejected from the Cochrane review of strategies to improve retention because it only included randomised evaluations. However, the systematic assessment of non-randomised evaluations may inform trialists' decision-making about retention methods that have been evaluated in a trial context.Therefore, we performed a systematic review to synthesise evidence from non-randomised evaluations of retention strategies in order to supplement existing randomised trial evidence.
We searched MEDLINE, EMBASE, and Cochrane CENTRAL from 2007 to October 2017. Two reviewers independently screened abstracts and full-text articles for non-randomised studies that compared two or more strategies to increase participant retention in randomised trials. The retention trials had to be nested in real 'host' trials ( including feasibility studies) but not hypothetical trials. Two investigators independently rated the risk of bias of included studies using the ROBINS-I tool and determined the certainty of evidence using GRADE (Grading of Recommendations Assessment, Development and Evaluation) framework.
Fourteen non-randomised studies of retention were included in this review. Most retention strategies (in 10 studies) aimed to increase questionnaire response rate. Favourable strategies for increasing questionnaire response rate were telephone follow-up compared to postal questionnaire completion, online questionnaire follow-up compared to postal questionnaire, shortened version of questionnaires versus longer questionnaires, electronically transferred monetary incentives compared to cash incentives, cash compared with no incentive and reminders to non-responders (telephone or text messaging). However, each retention strategy was evaluated in a single observational study. This, together with risk of bias concerns, meant that the overall GRADE certainty was low or very low for all included studies.
This systematic review provides low or very low certainty evidence on the effectiveness of retention strategies evaluated in non-randomised studies. Some strategies need further evaluation to provide confidence around the size and direction of the underlying effect.
参与者的保留对于确保临床试验的统计效力和内部有效性至关重要。较差的参与者保留会降低效力,并可能影响干预效果的估计。目前,从随机比较中获得的有效策略来保留随机试验中的参与者的证据很少。目前,由于仅包括随机评估,因此从宿主临床试验中嵌入的试验保留干预措施的非随机评估被 Cochrane 审查策略拒绝,以提高保留率。然而,对非随机评估的系统评估可能会为试验人员提供有关已在试验环境中评估的保留方法的决策信息。因此,我们进行了系统评价,以综合保留策略的非随机评估证据,以补充现有的随机试验证据。
我们从 2007 年至 2017 年 10 月搜索了 MEDLINE、EMBASE 和 Cochrane CENTRAL。两名审查员独立筛选了摘要和全文文章,以比较两种或多种策略,以增加随机试验中的参与者保留率。保留试验必须嵌套在实际的“宿主”试验(包括可行性研究)中,而不是假设性试验。两名调查人员使用 ROBINS-I 工具独立评估纳入研究的偏倚风险,并使用 GRADE(推荐评估、制定和评估分级)框架确定证据的确定性。
本综述共纳入了 14 项关于保留的非随机研究。大多数保留策略(在 10 项研究中)旨在提高问卷的回复率。与邮寄问卷完成相比,电话随访有利于提高问卷的回复率,与邮寄问卷相比,在线问卷随访有利于提高问卷的回复率,与较长的问卷相比,较短的问卷有利于提高问卷的回复率,与现金奖励相比,电子转账的金钱奖励有利于提高问卷的回复率,与没有奖励相比,提醒非应答者(电话或短信)有利于提高问卷的回复率。然而,每种保留策略都在单个观察性研究中进行了评估。这一点,再加上偏倚风险的考虑,意味着所有纳入研究的总体 GRADE 确定性都很低或非常低。
本系统评价提供了在非随机研究中评估保留策略的有效性的低或非常低确定性证据。一些策略需要进一步评估,以提供对潜在效果的大小和方向的信心。