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CBT Versus a Return to Work Intervention for Patients With Common Mental Illness in Primary Care

Cognitive Behavior Therapy Versus a Return to Work Intervention for Sick-listed Patients With Common Mental Illness in Primary Care: a Randomized Clinical Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01636791
Acronym
CBT vs RTW I
Enrollment
211
Registered
2012-07-10
Start date
2012-09-30
Completion date
2015-12-31
Last updated
2016-03-03

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

Conditions

Anxiety Disorders, Major Depression, Primary Insomnia, Stress Disorders

Brief summary

Background: Common mental illness, such as anxiety disorders and depression, is the main cause for sick leave in Sweden. Cognitive behavior therapy (CBT) has been shown to be effective in alleviating target symptoms of these disorders, but its effect on sick leave rates has not been sufficiently addressed. The investigators have developed an intervention called return to work (RTW), which is based in cognitive behavioral theory, that has a primary aim of helping sick-listed patients with common mental illness return to work. This new treatment has not been evaluated in a randomized controlled trial. Aims: The aim of this study is to investigate the effect of CBT and RTW for common mental illness in a randomized controlled trial conducted in primary care. Participants will be randomized to diagnosis specific CBT (n=70), RTW (n=70), or a combination of the two treatments (n=70). Main outcomes are days of sick leave and clinician severity rating of psychiatric symptoms. This study could contribute to new knowledge regarding how to best treat patients on sick leave with common mental illness.

Interventions

BEHAVIORALCognitive behavior therapy

Cognitive behavior therapy entails psychoeducational components, i.e. the patient is learns about the disorder and how to view it from a cognitive behavioral perspective. The most important part of the treatment is systematic behavior changes often targeted at exposure to feared stimuli. This is combined with cognitive interventions targeted at challenging negative automatic thoughts. All treatments will be delivered by licensed psychologists.

BEHAVIORALReturn to work

Participants randomized to this arm will receive an experimental treatment, based in cognitive behavioral therapy, with primary aim to help patients return to work. Interventions are aimed at solving work-related problems and comprises problem-solving training and systematic employer-patient meetings aimed at facilitating a gradual return to the workplace. Licensed psychologists deliver all treatments.

Sponsors

Region Stockholm
CollaboratorOTHER_GOV
Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Have been on sick leave (at least 50%) for at least 1 month and not more than 6 months * Have an anxiety disorder diagnosis (obsessive compulsive disorder, social phobia, panic disorder, generalized anxiety disorder, post-traumatic stress disorder, specific phobia), or/and major depression, or/and maladaptive stress reaction, or/and primary insomnia

Exclusion criteria

* A lower score than 4 on the Clinician severity rating scale * A higher score than 6 on the Clinician severity rating scale

Design outcomes

Primary

MeasureTime frameDescription
Clinician Severity Rating (CSR)Baseine, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in CSR at post-treatment, 26 week follow-up, and 52 week follow-up compared to baseline.
Sick leave1 yearNumber of days on sick leave

Secondary

MeasureTime frameDescription
Work ability index (WAI)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in WAI at post-treatment, 26 week follow-up, 52 week follow-up
Insomnia Severity Index (ISI)Baseline, post-treatment (variable depending on disorder, 26 week follow-up, 52 week follow-upChange in ISI at post-treatment, 26 week follow-up, and 52 week follow-up
Health Anxiety Inventory (HAI)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in HAI at post-treatment, 26 week follow-up, and 52 week follow-up
Perceived Stress Scale (PSS)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in PSS at post-treatment, 26 week follow-up, and 52 week follow-up
Trimbos and Institute of Technology Cost Questionnaire for Psychiatry (TIC-P)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in TIC-P at post-treatment, 26 week follow-up, and 52 week follow-up
Quality of Life Inventory (QOLI)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in QOLI at post-treatment, 26 week follow-up, and 52 week follow-up
EuroQol-5 dimension (EQ5D)Baseline, post-treatment (variable depending on disorder), 26 feel follow-up, 52 week follow-upChange in EQ5D at post-treatment, 26 week follow-up, and 52 week follow-up
Self-rated health 5 (SRH-5)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in SRH-5 at post-treatment, 26 week follow-up and 52 week follow-up
Obsessive Compulsive Inventory-Revised (OCI-R)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in OCI-R at post-treatment, 26 week follow-up, and 52 week follow-up. Disorder specific.
Liebowitz Social Anxiety Scale Self-report (LSAS-SR)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in LSAS-SR at post-treatment, 26 week follow-up, and 52 week follow-up. Disorder specific.
Panic Disorder Severity Scale Self-rated (PDSS-SR)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in PDSS-SR at post-treatment, 26 week follow-up, and 52 week follow-up. Disorder specific.
Penn-State Worry Questionnaire (PSWQ)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in PSWQ at post-treatment, 26 week follow-up, and 52 week follow-up. Disorder specific.
Post Traumatic Stress Disorder Symptom Scale-Self report (PTSDSS)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in PTSDSS at post-treatment, 26 week follow-up, and 52 week follow-up. Disorder specific.
Sheehan Disability Scales (SDS)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in SDS at post-treatment, 26 week follow-up, and 52 week follow-up
Montgomery-Åsberg Depression Rating Scale-Self-report (MADRS-S)Baseline, post-treatment (variable depending on disorder), 26 week follow-up, 52 week follow-upChange in MADRS-S at post-treatment, 26 week follow-up, and 52 week follow-up

Other

MeasureTime frameDescription
Inflammatory cytokinesBaseline, post-treatment (variable depending on disorder)Change in inflammatory cytokines at post-treatment

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026