- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04350983
Physical Activity on Prescription and Enhanced Individual Support by Physiotherapist
Physical Activity on Prescription and Enhanced Individual Support by Physiotherapist A Comparative Study Between Individuals With One Diagnosis and Multimorbidity
Multimorbidity is common, especially in the elderly population and is associated with a higher risk of mortality and disability, lower quality of life, polypharmacy, increased healthcare use and costs. Physical inactivity increases the risk of multimorbidity and individuals with multimorbidity are more likely to be physically inactive. Physical activity can prevent and treat several diseases. Physical Activity on Prescription (PAP) is an evidence-based method used in health care to increase physical activity. The aim of this study was to investigate whether self-reported physical activity level increase and sedentary time decreases in individuals who have received PAP in health care completed with enhanced individual support by physiotherapist at PAP-reception in wellness center for six months and to compare individuals with one diagnosis to individuals with multimorbidity.
The study population consisted of 331 adults who received PAP in health care and enhanced individual support by a physiotherapist at PAP-reception during six months. Data has been collected retrospectively from a local register with questionnaires from the PAP-reception. Self reported physical activity minutes/week and hours of sedentary time/day were measured at baseline and at six months. Differences in physical activity minutes and sedentary time from baseline to six months have been compared between individuals with one diagnosis and individuals with multimorbidity.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Received physical activity on prescription from health care
- Contact with PAP-reception
Exclusion Criteria:
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical activity minutes/week
Time Frame: Change between baseline and six months follow up.
|
Self-assessment of two physical activity questions
|
Change between baseline and six months follow up.
|
|
Sedentary time hours/day
Time Frame: Change between baseline and six months follow up.
|
Self-assessment of one sedentary behaviour question
|
Change between baseline and six months follow up.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Diagnoses
Time Frame: Measured at baseline
|
Type and number of diagnoses
|
Measured at baseline
|
|
Visits and telephone contacts
Time Frame: Measured at six months follow up
|
Number of visits and telephone contacts
|
Measured at six months follow up
|
|
Socia demographic data
Time Frame: Measured at baseline
|
Age (years), sex (female/male)
|
Measured at baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Maria Larsson, PhD, Sahlgrenska academy, University of Gothenburg
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PAP enhanced support 271821
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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