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Clinical Trial Summary

The main hypothesis:

The participants receive treatment at Beitostølen within 8 weeks or within 16 weeks. The groups waiting for rehabilitation is compared with the group receiving rehabilitation


Clinical Trial Description

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Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01788397
Study type Interventional
Source Beitostølen Health Sports Center
Contact
Status Completed
Phase N/A
Start date September 2010
Completion date December 2014

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