- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00369135
Cross-Disciplinary Workplace Intervention Strategy for Chronic Musculoskeletal Disorders
Sickness absenteeism caused by MSDs is a persistent and expensive health challenge in all industrial countries including Switzerland. Despite much progress as to the cause and prevention of MSDs, they continue to be some of the most prevalent and challenging health problems with respect to the work-place and to socio-economic burden.
To improve the situation, several recent reviews recommended interventions based on the bio-psycho-social model. Work-hardening and industrial rehabilitation programs focused more on the in balance between physical and mental demands of work on one side and capacities of the individual on the other side. Therefore we propose to merge the two models into one. The result is an interdisciplinary intervention strategy witch includes work hardening, medical trainings, a cognitive behavioural approach and work place intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Lausanne, Switzerland
- Recruiting
- Institut universitaire romand de Santè au Travail
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Employees on sick leave because of non-specific back and/or neck/shoulder pain
- actual unable to work and continuous or cumulative (totalized) work incapa- city in the past 6 monts
- ≥ 20 working days 100% absence from work or
- ≥ 40 working days 80 to 99% absence from work or
- ≥ 60 working days 50 to 79% absence from work and
- not older than 58 level of employment ≥ 50%
- no longer than 6 monts absencer from work (100% unable to work)
Exclusion Criteria:
- Specific diagnosis such as infection, neoplasm, metastasis osteoporosis, rheumatoid arthritis, fracture and inflammatory process or other conditions for which valid diagnoses had been demonstrated either in the anamnesis, records or the clinical examination
- Postoperative health condition with prohibited physical load
- Major co-morbidity which may determine return to work in a clearly stronger way then the MSD itself such as a major depression, psychosis, heavy drug or alcohol disease or instable cardiac or pulmonary disease
- Predominant specific shoulder pathology in "neck-shoulder pain"
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Sick-day saving, work capacity, economic variables
Time Frame: one year
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Functional performance, pain, general health, variables related to coping, believes, anxiety, depression
Time Frame: one year
|
one year
|
Collaborators and Investigators
Investigators
- Study Director: Danuser Brigitta, Prof, Institut universitaire romand de Santè au Travail
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NFP-111-111
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