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临床试验/NCT06397326
NCT06397326已完成不适用

Sustainable and Healthy Return-to-Work Program for Employees of Large Healthcare Organizations - PRATICAdr 2.0

Université du Québec a Montréal1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2024年5月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
49
试验地点
1
主要终点
Sick leave duration

研究概览

简要总结

This study aims to assess the effectiveness of PRATICAdr 2.0, a web application facilitated by a Return-to-Work Coordinator (RTW-C), with a focus on reducing sick leave duration and preventing relapse in individuals with CMDs. PRATICAdr 2.0 designed to enhance collaboration among Return-to-Work (RTW) stakeholders and provide systematic support throughout the RTW process, is evaluated in a randomized control trial (RCT). As part of the RCT, a total of 80 sick leave employees from 4 large public health organizations (n=80, 40 from the experimental group and 40 from the control group) will be recruited. The control group receives usual services offered by a RTW-C to sick leave employees, while the experimental group receives RTW-C services plus the use of PRATICAdr 2.0.

详细描述

Common mental disorders (CMDs) are highly prevalent in workplace settings, and have become a significant public health challenge. This study aims to assess the effectiveness of PRATICAdr 2.0, a web application facilitated by a Return-to-Work Coordinator (RTW-C), with a focus on reducing sick leave duration and preventing relapse in individuals with CMDs. PRATICAdr 2.0 designed to enhance collaboration among Return-to-Work (RTW) stakeholders and provide systematic support throughout the RTW process, is evaluated in a randomized control trial (RCT). As part of the RCT, a total of 80 sick leave employees from 4 large public health organizations (n=80, 40 from the experimental group and 40 from the control group) will be recruited. The control group receives usual services offered by a RTW-C to sick leave employees, while the experimental group receives RTW-C services plus the use of PRATICAdr 2.0. Participants will be randomly assigned to either the PRATICAdr 2.0 experimental group or the control group using computerized stratified randomization based on age, site, and sex (sealed envelope method). Participants will complete a series of online questionnaires at several following time points. Survival analyses were used to compare sick leave durations and relapses between the experimental group (PRATICAdr with RTW-C), and control groups (RTW-C only). Mixed linear models were used to observe changes in clinical symptoms over time, especially for the experimental group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Sick leave due to Common mental disorder (i.e. depression, anxiety, adjustment disorder, burnout)
  • Sick leave duration (from 1 to 3 months)
  • Member of participating unions in the large health organization

排除标准

  • Inability to communicate in French
  • Have a known organic disorder
  • Have a professional dirsorder (CNESST)
  • Have experienced previous sick leaves due to Common mental disorder

研究组 & 干预措施

Return to work coordinator only

Sham Comparator

The primary objective of the Return to work coordinator (RTW-C) is to coordinate, plan, and promote sustainable RTW for employees on sick leave.The RTW-C is responsible for assessing employee functioning while exploring barriers to RTW and available resources to develop a RTW plan. Also, RTW-C enhance communication and collaboration among stakeholders involved in the RTW process.

In this arm, the RTW-C does not use PRATICAdr 2.0.

干预措施: Return to work coordinator only (Behavioral)

Return to work coordinator + PRATICAdr 2.0

Experimental

The primary objective of the Return to work coordinator (RTW-C) is to coordinate, plan, and promote sustainable RTW for employees on sick leave.The RTW-C is responsible for assessing employee functioning while exploring barriers to RTW and available resources to develop a RTW plan. Also, RTW-C enhance communication and collaboration among stakeholders involved in the RTW process.

In this arm, the RTW-C uses PRATICAdr 2.0, a web application including key features (e.g., Facilitation of collaboration among multiple RTW stakeholders across healthcare, enterprise, and insurance sectors; Integration of each stakeholder's action into the sick leave employee's RTW process; sequential process aligned with the three phases of the RTW, inclusion of tools).

干预措施: Return to work coordinator + PRATICAdr 2.0 (Behavioral)

结局指标

主要结局

Sick leave duration

时间窗: through study completion, an average of 2 years

The number of days during the sick leave

Relapses

时间窗: through study completion, an average of 2 years

Number of relapses after returning to work

次要结局

  • Return to Work Obstacles and Self-Efficacy(through study completion, an average of 2 years)
  • Depressive symptoms(through study completion, an average of 2 years)
  • Anxiety symptoms(through study completion, an average of 2 years)

研究者

发起方
Université du Québec a Montréal
申办方类型
Other
责任方
Principal Investigator
主要研究者

Marc Corbière

Full professor

Université du Québec a Montréal

研究点 (1)

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