Effectiveness of adding 'exposure in vivo' techniques to the return-to-work plan of workers with mental health problems: a cluster randomised controlled trial
| ISRCTN | ISRCTN72643128 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN72643128 |
| Protocol serial number | N/A |
| Sponsor | Academic Medical Centre (AMC) (The Netherlands) |
| Funder | Knowledge centre on reintegration for professionals (Stichting Expertise Centrum Reintegratie [STECR]) (The Netherlands) - Aladdin Program |
- Submission date
- 11/04/2007
- Registration date
- 11/04/2007
- Last edited
- 13/09/2013
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr F W Noordik
Scientific
Scientific
Academic Medical Centre
University of Amsterdam
Coronel Institute of Occupational Health
Amsterdam
1100 DE
Netherlands
| Phone | +31 (0)20 566 4878 |
|---|---|
| f.w.noordik@amc.nl |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised, active controlled, parallel group, multicentre trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study acronym | Work up study |
| Study objectives | Occupational rehabilitation with a gradual return to work based on the principles of exposure in vivo will be more (cost)-effective in reducing absenteeism than usual occupational rehabilitation. |
| Ethics approval(s) | Ethics approval received from the local medical ethics committee |
| Health condition(s) or problem(s) studied | Return to work of workers with common mental health complaints |
| Intervention | Level of occupational physician: 1. Two days of training followed by three intervision meetings Level of worker: 1. Information folder with rationale 2. Homework assignments 3. Meeting with supervisor |
| Intervention type | Other |
| Primary outcome measure(s) |
1. Time to full return to work |
| Key secondary outcome measure(s) |
1. Psychological complaints |
| Completion date | 01/01/2009 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Not Specified |
| Target sample size at registration | 200 |
| Key inclusion criteria | Workers who: 1. Are two to six 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 |
| Key exclusion criteria | Workers with: 1. Severe mental illnesses (psychotic disorders, bipolar disorder) 2. Post Traumatic Stress Disorder (PTSD) 3. Addiction problems 4. A primary somatic disorder |
| Date of first enrolment | 01/01/2007 |
| Date of final enrolment | 01/01/2009 |
Locations
Countries of recruitment
- Netherlands
Study participating centre
Academic Medical Centre
Amsterdam
1100 DE
Netherlands
1100 DE
Netherlands
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results | 01/03/2013 | Yes | No |