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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: Netherlands Trial Register
Last refreshed on: 28 April 2013
Main ID:  NTR874
Date of registration: 22/01/2007
Primary sponsor: Academic Medical Center (AMC), Coronel Institute for Occupational and Environmental Health
Public title: Efectiveness of adding 'exposure in vivo' techniques to the return-to-work plan of workers with mental health problems: a cluster randomised controlled trial.
Scientific title: Efectiveness of adding 'exposure in vivo' techniques to the return-to-work plan of workers with mental health problems: a cluster randomised controlled trial. - work up study
Date of first enrolment: 1/1/2007
Target sample size: 200
Recruitment status: recruiting
URL:  http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=874
Study type:  intervention
Study design:  Randomised: Yes; Masking: None; Control: Active; Group: Parallel; Type: -  
Countries of recruitment
The Netherlands
Contacts
Name: F.W.  Noordik
Address:  Academic Medical Center, University of Amsterdam: Coronel Institute of occupational health. , PO Box 22700 1100 DE Amsterdam The Netherlands
Telephone: +31 20 5664878
Email: f.w.noordik@amc.nl
Affiliation: 
Name: F.W.  Noordik
Address:  Academic Medical Center, University of Amsterdam: Coronel Institute of occupational health. , PO Box 22700 1100 DE Amsterdam The Netherlands
Telephone: +31 20 5664878
Email: f.w.noordik@amc.nl
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: Workers who:
1. are 2-6 weeks absent from work;
2. have either:
a. a stress-related disorder (defined as having at least one psychological complaint with significant suffering or problems with functioning);
b.an anxiety disorder;
c. a depressive disorder.

Exclusion criteria: Workers with:
1. severe mental illnesses (psychotic disorders, bipolar disorder);
2. PTSD;
3. addiction problems;
4. a primary somatic disorder.


Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
Sick leave, Reintegration, Mental health complaints, Exposure in vivo, Anxiety

Intervention(s)
Level of occupational physician:
1. Two days of training followed by 3 intervision meetings
Level of worker:
1. Information folder with rationale;
2. Homework assignments;
3. Meeting with supervisor
Primary Outcome(s)
1. Time to full return to work;
2. Time to relapse;
3. Pecentage of contract hours worked;
4. Work functioning.
Secondary Outcome(s)
1. Psychological complaints;
2. Work ability;
3. Self efficacy in returning to work;
4. Coping with work situations;
5. Avoidance of work situations;
6. Work adjustments;
7. Satisfaction of worker with occupational physician.
Secondary ID(s)
ISRCTN72643128
Source(s) of Monetary Support
STECR Alladin Program
Secondary Sponsor(s)
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