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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05963308
Enrollment
123
Registered
2023-07-27
Start date
2023-03-06
Completion date
2026-03-01
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Brief 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.

Interventions

BEHAVIORALHealthy Minds

The group intervention (approximately 5 participants per group, 8 groups) is facilitated by two clinicians and 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: Week1: Coping with work stress at work W2 and W3: Recognizing and modifying my dysfunctional beliefs linked to work W4: Overcoming obstacles linked to work functioning and maintaining work W5: To put in place needed work accommodations with the support of the immediate supervisor W6: My strengths and competencies related to work W7: Accepting criticism and asserting myself appropriately W7: My strengths and related skills W8: My best coping strategies for work Both intervention and control participants receive their standard individualized care from their clinician. However, for the experimental participants, the Healthy Minds intervention is an added component to their regular care.

Sponsors

Université du Québec a Montréal
Lead SponsorOTHER
PhysioExtra
CollaboratorUNKNOWN
Energir
CollaboratorUNKNOWN
Ciusss de L'Est de l'Île de Montréal
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Be in the process of returning to work after depression, anxiety disorder, adjustment disorder (with depressed mood, or anxious mood). or * Been back for less than a month

Exclusion criteria

* Inability to communicate in French * Have a known organic disorder * Have already received CBT-type intervention (group or individual)

Design outcomes

Primary

MeasureTime frameDescription
Sustainable return-to-workBaseline; follow-ups at six months and 12 monthsThe number of days of job retention after returning to work
Depressive symptomsBaseline; follow-ups at two months, six months and 12 monthsPatient Health Questionnaire for depression (PHQ-9)
Anxiety symptomsBaseline ; follow-ups at two months, six months and 12 monthsGeneralized Anxiety Disorder Scale (GAD-7)
Work functioningFollow-ups at six months and 12 monthsEndicott Work Productivity Scale (EWPS)
Relationship with immediate supervisorFollow-ups at six months and 12 monthsInventory of perceptions of supervisory style at work
Work accommodationsFollow-ups at six months and 12 monthsThe Work Accommodation and Natural Support Scale (WANSS).
Return to Work Obstacles and Self-EfficacyBaseline ; Follow-ups at two monthsReturn to Work Obstacles and Self-Efficacy Scale (ROSES)
Cognitive difficultiesBaseline ; Follow-ups at two months, six months and 12 monthsOnline Stroop test (French version)
Cognitive biasesBaseline ; Follow-ups at two months, six months and 12 monthsDavos Assessment of the Cognitive Biases Scale

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORMarc Corbière, PhD

Université du Québec a Montréal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026