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基于 iJobs 的网络心理教育干预提高失业人群求职行为和促进心理健康的效果:一项等待期随机对照试验的研究方案。

Efficacy of the iJobs Web-Based Psychoeducational Intervention to Improve Job Search Behavior and Promote Mental Health Among Unemployed People: Protocol for a Waitlist Randomized Controlled Trial.

机构信息

Department of Psychology, West University of Timișoara, Timișoara, Romania.

Department of Work and Organization Studies, KU Leuven, Brussels, Belgium.

出版信息

JMIR Res Protoc. 2024 May 8;13:e55374. doi: 10.2196/55374.

Abstract

BACKGROUND

Unemployment affects millions of people worldwide and, beyond its economic impact, has severe implications for people's well-being and mental health. Different programs have been developed in response to this phenomenon, but to date, job-search interventions have proved to be most effective, especially the JOBS II program. The JOBS II program proved not only to be effective for re-employment but also has a positive impact on beneficiaries' mental health (ie, reduces anxiety or depression). However, by now, this evidence-based program has been delivered only on site in the various countries where it was implemented. In the digital era, web-based alternatives to such programs are highly needed because they have the advantages of scalability and cost-effectiveness.

OBJECTIVE

In this context, we aim to investigate the efficacy of iJobs, the web-based adaptation of the JOBS II program, on job-search intensity and effort, the quality of job-search behaviors, and job-search self-efficacy. Further, 1 month after the intervention, we will also assess the employment status and the satisfaction with the job (if applicable). This study will also investigate the effect of iJobs on well-being and mental health (ie, anxiety and depression).

METHODS

This study is a 2-arm randomized controlled trial. The 2 independent groups (intervention vs waiting list control group) will be crossed with 3 measurement times (ie, baseline, the postintervention time point, and 1-month follow-up). The design will be a 2 (intervention vs control) × 3 (baseline, the postintervention time point, and 1-month follow-up) factorial design. iJobs is a 2-week intervention consisting of 6 modules: an introductive module and 5 modules adapted from the original JOBS II program to the web-based setting and Romanian population. The web-based intervention also has a human component, as beneficiaries receive personalized written feedback after each module on the platform from a team of psychologists involved in the project.

RESULTS

The enrollment of study participants started in June 2023 and is expected to end in May 2024. The data collection is expected to be completed by July 2024. The results are expected to be submitted for publication in the summer of 2024.

CONCLUSIONS

This study is the first large-scale randomized controlled trial aiming to test the efficacy of a web-based adaptation of the JOBS II program. If our results support the efficacy of iJobs, they will offer the premise for it to become an evidence-based, accessible alternative for unemployed people in Romania and might be implemented in other countries.

TRIAL REGISTRATION

ClinicalTrials.gov NCT05962554; https://clinicaltrials.gov/study/NCT05962554.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/55374.

摘要

背景

失业影响着全球数百万人,除了其经济影响外,还对人们的福祉和心理健康产生严重影响。针对这一现象,已经开发了不同的项目,但迄今为止,求职干预措施被证明是最有效的,尤其是 JOBS II 项目。JOBS II 项目不仅被证明对重新就业有效,而且对受益人的心理健康也有积极影响(即,减轻焦虑或抑郁)。然而,到目前为止,这个基于证据的项目仅在实施它的各个国家现场提供。在数字时代,非常需要基于网络的此类项目替代方案,因为它们具有可扩展性和成本效益的优势。

目的

在这种情况下,我们旨在研究 iJobs(JOBS II 项目的网络版)在求职强度和努力、求职行为质量和求职自我效能方面的效果。此外,在干预后 1 个月,我们还将评估就业状况和对工作的满意度(如果适用)。本研究还将调查 iJobs 对幸福感和心理健康(即焦虑和抑郁)的影响。

方法

这是一项 2 臂随机对照试验。两个独立的组(干预组与等待名单对照组)将交叉 3 个测量时间(即基线、干预后时间点和 1 个月随访)。设计将是 2(干预组与对照组)× 3(基线、干预后时间点和 1 个月随访)的析因设计。iJobs 是一个为期 2 周的干预措施,包括 6 个模块:一个介绍性模块和 5 个从原始 JOBS II 项目改编到网络环境和罗马尼亚人口的模块。网络干预也有一个人为组成部分,因为受益人事后在平台上从参与项目的心理学家团队那里收到关于每个模块的个性化书面反馈。

结果

研究参与者的招募已于 2023 年 6 月开始,预计将于 2024 年 5 月结束。数据收集预计将于 2024 年 7 月完成。研究结果预计将在 2024 年夏季提交发表。

结论

这项研究是第一个旨在测试 JOBS II 项目网络版有效性的大规模随机对照试验。如果我们的结果支持 iJobs 的有效性,它们将为它成为罗马尼亚失业人员的循证、可及的替代方案提供前提,并可能在其他国家实施。

试验注册

ClinicalTrials.gov NCT05962554;https://clinicaltrials.gov/study/NCT05962554。

国际注册报告标识符(IRRID):PRR1-10.2196/55374。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4856/11112481/3a6cf75213c4/resprot_v13i1e55374_fig1.jpg

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