Skip to main content
Clinical Trials/NCT00594360
NCT00594360
Unknown
Phase 2

Exercise on Prescription: Effects and Comparison of Psychological Parameters Physical Activity, Physical Fitness, and Health Physical Between Participants in a Danish Version of Exercise on Prescription.

University of Southern Denmark1 site in 1 country200 target enrollmentNovember 2005

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Physical Inactivity
Sponsor
University of Southern Denmark
Enrollment
200
Locations
1
Primary Endpoint
Patient-reported Self-efficacy level at 4, 10 and 16 months. Patient-reported Decisional balance level at 4, 10 and 16 months. Patient-reported Readiness to change level at 4, 10 and 16 months.
Last Updated
18 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the effect of a primary healthcare intervention called 'Exercise on Prescription' aimed at increasing level of physical activity and psychological parameters in a population of sedentary patients with increased risk of developing lifestyle diseases. The effect is evaluated using patient-reported variables.

Detailed Description

Exercise prescriptions are used for initiating a physical active lifestyle in sedentary populations. A Danish project called 'Exercise on Prescription' (EoP) is implemented in primary healthcare. Patients eligible for EoP are non-institutionalised adults with medically controlled lifestyle diseases or risk factors of lifestyle diseases, who are motivated to change lifestyle, able to improve health status through a physical active lifestyle, and willing to pay a fee of €100 for the intervention. The purpose of this study is to assess the effect on: 1) Self-efficacy, 2) Readiness to change, 3) Decisional balance, 4) physical activity level, and 5) health related quality of life. The EoP-group is compared to an intervention group receiving only motivational counselling.

Registry
clinicaltrials.gov
Start Date
November 2005
End Date
May 2008
Last Updated
18 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All patients referred to the Exercise on Prescription scheme by their general practitioner
  • Volunteer to participate in the trial

Exclusion Criteria

  • BMI over 35

Outcomes

Primary Outcomes

Patient-reported Self-efficacy level at 4, 10 and 16 months. Patient-reported Decisional balance level at 4, 10 and 16 months. Patient-reported Readiness to change level at 4, 10 and 16 months.

Time Frame: 16 months

Secondary Outcomes

  • Patient-reported physical activity level at 4, 10 and 16 months. . Patient-reported health related quality of life at 4, 10 and 16 months. Patient-reported compliance with national guidelines for physical activity at 4, 10 and 16 months.(16 months)

Study Sites (1)

Loading locations...

Similar Trials