Recruitment rates, retention rates, and follow-up completion in a Brief Intervention and Contact trial for suicidal behavior: a feasibility study.

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Divya Soni, Balpreet Panesar, Alexander Dufort, Lucy Guan, Jennifer Lee, Dana Waldern, Stephanie Hathaway, Nitika Sanger, Sid Stacey, Luciano Minuzzi, Lehana Thabane, Zainab Samaan
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引用次数: 0

Abstract

Background: Suicide is a serious public health concern for which there are limited evidence-based interventions being employed. This feasibility study administered a Brief Intervention and Contact (BIC) trial adopted from the WHO Multisite Intervention Study on Suicidal Behaviors (SUPRE-MISS) and followed participants after they had been discharged from the inpatient hospital setting.

Aims: To assess the recruitment and retention rates, follow-up visit completion, barriers to recruitment and retention, resources needed of employing this study, and data completion.

Methods: Eligible participants were recruited from psychiatric inpatient settings, in Hamilton, Ontario. Adults with suicidal behavior were randomly allocated to BIC (intervention) plus treatment as usual (TAU) or treatment as usual (control) and were followed for 6 months. The intervention arm completed 9 follow-up points during the 6-month follow-up period post-discharge. Calculation of recruitment and retention rates and associated statistical analyses were completed using SPSS version 25.

Results: A total of 154 participants were approached during the 8-month recruitment period, 60 participants were enrolled resulting in a recruitment rate of 7.625 participants per month. A total of 61 participants were recruited, with 1 duplicate. The retention rate was 47.5% for the recruited participants at the end of the study.

Conclusions: Few suicide-based follow up interventions assess the feasibility of conducting the study. Retention was low for this study; however, participants outlined reasons for withdrawal that are consistent with other research areas related to mental health. Findings from this study will help inform suicide research on the barriers and challenges to participant recruitment and retention.

Trial registration: NCT03825354, Registered January 30 th, 2019, ClinicalTrial.gov; https://clinicaltrials.gov/study/NCT03825354?cond=suicide&term=brief%20intervention%20and%20contact&rank=6.

自杀行为的短期干预和接触试验的招募率、保留率和随访完成情况:可行性研究。
背景:自杀是一个严重的公共卫生问题,目前采用的循证干预措施有限。这项可行性研究采用了世卫组织自杀行为多地点干预研究(SUPRE-MISS)中的一项简短干预和接触(BIC)试验,并在参与者出院后对其进行随访。目的:评估招募和保留率、随访完成情况、招募和保留障碍、采用本研究所需的资源和数据完成情况。方法:从安大略省汉密尔顿的精神科住院病人中招募符合条件的参与者。有自杀行为的成年人被随机分配到BIC(干预)加常规治疗(TAU)或常规治疗(对照组),随访6个月。干预组在出院后6个月随访期内完成9个随访点。采用SPSS 25版软件进行入留率计算和相关统计分析。结果:在8个月的招募期内,共接触了154名参与者,60名参与者被招募,每月招募率为7.625名参与者。共招募受试者61人,每组1个重复。研究结束时,被招募的参与者的保留率为47.5%。结论:很少有基于自杀的随访干预评估进行研究的可行性。这项研究的保留率很低;然而,参与者概述了退出的原因,这些原因与与心理健康有关的其他研究领域一致。这项研究的结果将有助于为自杀研究提供有关参与者招募和保留的障碍和挑战的信息。试验注册:NCT03825354, 2019年1月30日注册,ClinicalTrial.gov;https://clinicaltrials.gov/study/NCT03825354?cond=suicide&term=brief%20intervention%20and%20contact&rank=6。
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来源期刊
Pilot and Feasibility Studies
Pilot and Feasibility Studies Medicine-Medicine (miscellaneous)
CiteScore
2.70
自引率
5.90%
发文量
241
审稿时长
9 weeks
期刊介绍: Pilot and Feasibility Studies encompasses all aspects of the design, conduct and reporting of pilot and feasibility studies in biomedicine. The journal publishes research articles that are intended to directly influence future clinical trials or large scale observational studies, as well as protocols, commentaries and methodology articles. The journal also ensures that the results of all well-conducted, peer-reviewed, pilot and feasibility studies are published, regardless of outcome or significance of findings. Pilot and feasibility studies are increasingly conducted prior to a full randomized controlled trial. However, these studies often lack clear objectives, many remain unpublished, and there is confusion over the meanings of the words “pilot” and “feasibility”. Pilot and Feasibility Studies provides a forum for discussion around this key aspect of the scientific process, and seeks to ensure that these studies are published, so as to complete the publication thread for clinical research.
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