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Return to Work After a Workplace-oriented Intervention for Patients on Sick Leave Due to Burnout

Reduction of Person-job Mismatch to Increase Work Capacity, by Education of, and Dialogue Between Involved Parties - Evaluation of an Intervention Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01039168
Acronym
ADA model
Enrollment
76
Registered
2009-12-24
Start date
2003-11-30
Completion date
2009-09-30
Last updated
2024-03-15

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

Conditions

Professional Burnout

Keywords

Burnout, Sick leave, Intervention study, Prospective study, Work

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.

Interventions

BEHAVIORALWorkplace dialogue
OTHERCare as usual

Sponsors

Swedish Council for Working Life and Social Research
CollaboratorOTHER
Lund University
CollaboratorOTHER
County Councils of Southern Sweden
CollaboratorUNKNOWN
Region Skane
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 63 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Return to work from sick leaveUp to 1,5 years post intervention completion

Secondary

MeasureTime frame
Self-rated health measures (only in the intervention group)Up to 1,5 years post intervention completion

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026