Reduction of Person-job Mismatch to Increase Work Capacity, by Education of, and Dialogue Between Involved Parties - Evaluation of an Intervention Program
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Professional Burnout
- Sponsor
- Region Skane
- Enrollment
- 76
- Locations
- 1
- Primary Endpoint
- Return to work from sick leave
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
The study aims to evaluate the effect on return to work of a workplace intervention with patients being treated for burnout. The intervention intends to reduce job-person mismatch through patient-supervisor communication.The hypothesis is that the intervention group will show a more favourable outcome than a control group with respect to return to work.
Detailed Description
Participants are consecutively recruited in co-operation with regional social insurance offices (RSIOs) in the two southern counties of Sweden. Persons accepting participation are clinically examined and interviewed of the course of events leading up to the burnout and the patient's expectations of changes necessary to facilitate return to work are recorded. The patient´s supervisor is then interviewed at the workplace, responding to the same questions on perceived main causes of the subordinate's sick leave and changes necessary to facilitate return to work. Finally, the core intervention takes place, namely a dialogue being initiated between the patient and the supervisor to find solutions to facilitate return to work. Out of those who do not want to participate, without giving any specific reason for that, a control group is matched by length and degree of sick leave at the time of the intervention.
Investigators
Eligibility Criteria
Inclusion Criteria
- •employment
- •sick leave at lest half time 2-6 months due to work related burnout
- •previously healthy
Exclusion Criteria
- •other somatic or psychiatric disease explaining the symptoms
Outcomes
Primary Outcomes
Return to work from sick leave
Time Frame: Up to 1,5 years post intervention completion
Secondary Outcomes
- Self-rated health measures (only in the intervention group)(Up to 1,5 years post intervention completion)