Study Stopped
Study was terminated according the study protocol end of 2007
Cost of Long Term Disability in Patients With Chronic Non-Specific Low Back Pain
1 other identifier
observational
174
1 country
1
Brief Summary
The purpose of the study was to determine the cost-effectiveness of a function-centred treatment (FCT) compared with a pain-centred treatment (PCT) in patients with chronic low back pain (LBP) in an in-patient setting. Follow-up lasted three years. Direct and indirect costs were recorded by questionnaires sent to health insurances, employers and Swiss Disability Insurance Company.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2006
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2008
CompletedFirst Submitted
Initial submission to the registry
March 27, 2008
CompletedFirst Posted
Study publicly available on registry
April 3, 2008
CompletedApril 3, 2008
March 1, 2008
1.9 years
March 27, 2008
March 31, 2008
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
cost- effectiveness
3 year follow-up
Study Arms (2)
FCT
Patients passing a function- centred rehabilitation
PCT
Patients passing a pain-centred rehabilitation
Interventions
The two groups passed an in-patient rehabilitation and a physiotherapy: FCT function-centred vs. PCT pain-centred
Eligibility Criteria
Tertiary rehabilitaton centre
You may qualify if:
- Chronic low back pain, sick leave of 6 weeks during the last 6 months
You may not qualify if:
- not able to perform a training program
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Klinik Valenslead
- University of Applied Sciences of Western Switzerlandcollaborator
- Zurich University of Applied Sciencescollaborator
Study Sites (1)
Rehabilitationszentrum Klinik Valens
Valens, Canton of St. Gallen, CH- 7317, Switzerland
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Stefan Bachmann, MD
Rehabilitationszentrum Klinik Valens
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
March 27, 2008
First Posted
April 3, 2008
Study Start
January 1, 2006
Primary Completion
December 1, 2007
Study Completion
February 1, 2008
Last Updated
April 3, 2008
Record last verified: 2008-03