Promoting Sustainable Return to Work Among Employees on Sick Leave Due to

Status Recruiting

Clinical Trial Summary

The purpose of this clinical trial is to evaluate the impact of an online group intervention called Healthy Minds in facilitating a sustainable return to work for individuals with a mood disorder. The study aims to answer the following key questions : - Does receiving the Healthy Minds online intervention lead to a more sustainable return to work compared to not receiving the intervention? - Are the health outcomes (e.g., depressive symptoms) and work-related outcomes (e.g., work functioning) of individuals who receive the Healthy Minds online intervention better than those who do not receive the intervention in the year following the intervention? Both experimental and control participants will be recruited at baseline while on sick leave (expected to return to work in less than one month) or recently returned to work (less than one month). Participants will complete a series of online questionnaires at the following time points : - Baseline - First follow-up (2 months after baseline) - Second follow-up (6 months after baseline) - Third follow-up (12 months after baseline) The questionnaires will cover the following areas : - Sociodemographic and biopsychosocial factors - Symptoms associated with the primary mood disorder - Cognitive difficulties and biaises - Self-efficacy related to return to work - Work accommodations and natural supports - Relationship with immediate supervisor - Work functioning - Return to work time (number of days away from work) Experimental participants will participate in the 2-month online Healthy Minds group intervention (cohort of 5 participants) between the baseline assessment and the first follow-up. The intervention consists of 8 sessions (one per week for 8 weeks), with each session focusing on a specific aspect of the return-to-work process from a cognitive-behavioral perspective.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Adjustment Disorder With Anxious Mood
Adjustment Disorders
Anxiety Disorders
Depression Anxiety Disorder

Clinical Trial Details

NCT number	NCT05963308
Study type	Interventional
Source	Université du Québec a Montréal
Contact	Marc Corbière, PhD
Phone	514-987-3000
Email	corbiere.marc@uqam.ca
Status	Recruiting
Phase	N/A
Start date	March 6, 2023
Completion date	March 1, 2025

View Details

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Promoting Sustainable Return to Work Among Employees on Sick Leave Due to a Mental Health Condition: Evaluation of the HealthyMinds Online Group Intervention

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms