Article Text
Abstract
Objectives Common mental disorders (CMDs) cause great individual suffering and long-term sick leave. Cognitive–behavioural therapy (CBT) effectively treats CMDs, but sick leave is not reduced to the same extent as psychiatric symptoms. Research results regarding return-to-work interventions (RTW-Is) and their effect on sick leave are inconclusive. The aim of this study was to evaluate CBT, a RTW-I and combined CBT and RTW-I (COMBO) for primary care patients on sick leave due to CMDs.
Methods Patients with CMDs (n=211) were randomised to CBT (n=64), RTW-I (n=67) or COMBO (n=80). Sick-leave registry data after 1 year and blinded Clinician's Severity Rating (CSR) of symptoms post-treatment and at follow-ups after 6 and 12 months were primary outcomes.
Results There was no significant difference between treatments in days on sick leave 1 year after treatment start (mean difference in sick-leave days range=9–27). CBT led to larger reduction of symptoms post-treatment (CSR; Cohen's d=0.4 (95% CI 0.1 to 0.8)) than RTW-I, whereas COMBO did not differ from CBT or RTW-I. At follow-up, after 1 year, there was no difference between groups. All treatments were associated with large pre-treatment to post-treatment improvements, and results were maintained at 1-year follow-up.
Conclusion No treatment was superior to the other regarding reducing sick leave. All treatments effectively reduced symptoms, CBT in a faster pace than RTW-I, but at 1-year follow-up, all groups had similar symptom levels. Further research is needed regarding how CBT and RTW-I can be combined more efficiently to produce a larger effect on sick leave while maintaining effective symptom reduction.
- return-to-work
- cognitive behavioural therapy
- common mental disorders
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Footnotes
Contributors SS and EH designed the study, developed the treatment, performed the analyses, collected and interpreted the data, and drafted the paper. FS, EL, LGÖ, ML, MI, KE and BL designed the study,developed the treatment, collected and interpreted the data, and drafted the paper.
Funding This study was funded by Karolinska Institutet and by research grants from Stockholm County Council. The main funding organisations (Karolinska Institutet and Stockholm County Council) are public institutions and neither of the funding organisations had any role in the design and conduct of the study, in the collection or interpretation of the data, neither in the writing of the report nor in the decision to submit it.
Competing interests None declared.
Patient consent Obtained.
Ethics approval The regional ethics review board in Stockholm.
Provenance and peer review Not commissioned; externally peer reviewed.