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Clinical Trials/NCT01788397
NCT01788397CompletedNot Applicable

Effect of Comprehensive Rehabilitation at Beitostølen Healthsports Centre. A Randomized Study.

Beitostølen Health Sports Center2 sites in 1 country247 target enrollmentStarted: September 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
247
Locations
2
Primary Endpoint
Quality of life

Study Overview

Brief 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

Detailed Description

nn

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Investigator)

Eligibility Criteria

Ages
18 Years to 67 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients with physical disabilities admitted to treatment at BHC

Exclusion Criteria

  • Patients with severe cognitive disorders

Arms & Interventions

Physical activity

Experimental

Physical activity 2-4 times pr. day

Intervention: Physical activity (Behavioral)

Control group

No Intervention

No intervention in the control group

Outcomes

Primary Outcomes

Quality of life

Time Frame: Eight weeks

Short Form 12 v2

Secondary Outcomes

  • Pain(8 weeks)
  • Behavioural Regulation in Exercise Questionnaire (BREQ 2)(8 weeks)
  • Physical Activity Scale for Individuals with Physical Disabilities (PASIPD)(8 weeks)

Investigators

Sponsor
Beitostølen Health Sports Center
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hakon Dalen

MD

Beitostølen Health Sports Center

Study Sites (2)

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