Effect of Comprehensive Rehabilitation at Beitostølen Healthsports Centre

Physically Disabled Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01788397
• Other study ID #: BHSS
• Status: Completed
• Phase: N/A
• First received: February 7, 2013
• Last updated: January 11, 2015
• Start date: September 2010
• Est. completion date: December 2014

Study information

• Verified date: January 2015
• Source: Beitostølen Health Sports Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: Norway: Ethics Committee
• Study type: Interventional

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

Description:

nn

Recruitment information / eligibility

• Status: Completed
• Enrollment: 247
• Est. completion date: December 2014
• Est. primary completion date: December 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 67 Years

Eligibility

Inclusion Criteria:

• Patients with physical disabilities admitted to treatment at BHC

Exclusion Criteria:

• Patients with severe cognitive disorders

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

• Physically Disabled

Intervention

Behavioral:
• Physical activity
Swimming, physiotherapy, water therapy, alpine skiing, xc-skiing, hippotherapy, climbing, cycling, rowing

Locations

Country	Name	City	State
Norway	Beitostolen Healtsports Centre	Beitostolen	Oppland

Sponsors (2)

Lead Sponsor	Collaborator
Beitostølen Health Sports Center	Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Self efficacy	Self-Efficacy for Managing Chronic Disease 6-Item Scale; Exercise Regularly Scale (3-item scale); Social/Recreational Activities Scale (2-item scale); Stanford Patient Education Research Centre: Lorig K, Stewart A, Ritter P, González V, Laurent D, & Lynch J, Outcome Measures for Health Education and other Health Care Interventions. Thousand Oaks CA: Sage Publications, 1996, pp.24-25,41-45.	8 weeks	No
Primary	Quality of life	Short Form 12 v2	Eight weeks	No
Secondary	Pain	VAS Pain	8 weeks	No
Secondary	Behavioural Regulation in Exercise Questionnaire (BREQ 2)	Measures motivational regulation	8 weeks	No
Secondary	Physical Activity Scale for Individuals with Physical Disabilities (PASIPD)	Measures Physical Activity level	8 weeks	No