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At Work and Coping - Effect Study of Workcoping for Patients With Anxiety and Depression

At Work and Coping - Effect Evaluation of Center for Workcoping for Patients With Anxiety and Depression

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01146730
Acronym
AWaC
Enrollment
1202
Registered
2010-06-17
Start date
2010-06-30
Completion date
2018-05-31
Last updated
2018-07-11

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

Conditions

Anxiety, Depression

Keywords

Anxiety, Depression, Vocational Rehabilitation, Common Mental Disorders, Mental Health Problems, Work Related Therapy

Brief summary

Mental disorders, mainly various anxiety and depressive disorders, are an increasing reason for sick leave and disability pension. Cognitive behaviour therapy (CBT) has been shown to have an effect on anxiety and depression, but the investigators know little about this in relation to employment. Close follow-up in ordinary employment increase employment participation for serious mental illness, but this is not yet investigated to the same degree for lighter mental disorders. Center for Work-Coping (No: Senter for Jobbmestring - SJM) combines Cognitive behaviour therapy (CBT) and individual placement and support (IPS) and facilitation of work for people with anxiety and depression who are in danger of falling out of work. The purpose of this project is to evaluate the effectiveness of the model in SJM. The effect will be evaluated through a randomized controlled trial (RCT) in which participants will be randomized to SJM or regular follow-up by The Norwegian Labour and Welfare Administration (NAV) or by their regular general practitioners (GP) and self-help resources. The main outcome measures are work participation with changes in mental health as a secondary outcome.

Interventions

BEHAVIORALWorkcoping and IPS

Maximum 15 sessions of CBT-based counseling with workcoping as primary focus in addition to work support according to the IPS-model (individual placement and support)

BEHAVIORALOrdinary care by GP or NAV

Ordinary care by the participants physician or the local Labour and Welfare Administration

Sponsors

Norwegian Labour and Welfare Administration
CollaboratorOTHER
NORCE Norwegian Research Centre AS
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Problems coping with work due to psychological illness (anxiety and depression) * Reasonable closeness to work (possible to return within a year)

Exclusion criteria

* Other reasons as primary cause of work problems * Serous psychiatric disorders * Suicide risk * Pregnancy * Ongoing psychological treatment (therapy) * Ongoing substance abuse

Design outcomes

Primary

MeasureTime frameDescription
Sick leave dataOne yearThe primary outcome of the study is return to work measured through register data.

Secondary

MeasureTime frameDescription
Psychopathology6 and 12 months of follow upSecondary outcomes are reductions in psychopathology measured through validated questionnaires (e.g. HADS).

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026