ADL- Training for Patients With Chronic Obstructive Pulmonary Disease (COPD)
June 22, 2010 updated by: LHL Helse
Activities of Daily Living (ADL)-Training for Patients With Chronic Obstructive Pulmonary Disease (COPD)
ADL training of copd patients results in better execution of activities of daily living.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
24
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Hakadal, Norway, 1485
- Glittreklinikken
-
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Akershus
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Hakadal, Akershus, Norway, 1485
- Glittreklinikken
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- COPD
- Referred for rehabilitation
- Age > 18 years
- Symptoms affecting ADL function
- 6 minute walk distance (6MWD) < 400 meters
Exclusion Criteria:
- Patients who smokes or has smoked during the last three months.
- LTOT
- Patients who has another disability
- Patients who can't read or speak Norwegian
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: 1: Standard rehabilitation programme
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|
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Experimental: 2. Additional ADL training
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The control group gets the standard rehabilitation programme which includes one hour ADL- training.
The experimental group also gets the standard rehabilitation program, but instead of one hour they get an additional five hours ADL- training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Canadian Occupational Performance Measure(COPM) - Self-perception of occupational performance and satisfaction.
Time Frame: Baseline, 4 weeks; 3 months
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Baseline, 4 weeks; 3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Morten S Ryg, Dr philos, LHL Helse
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2009
Primary Completion (Actual)
February 1, 2010
Study Completion (Actual)
June 1, 2010
Study Registration Dates
First Submitted
April 14, 2009
First Submitted That Met QC Criteria
April 23, 2009
First Posted (Estimate)
April 24, 2009
Study Record Updates
Last Update Posted (Estimate)
June 23, 2010
Last Update Submitted That Met QC Criteria
June 22, 2010
Last Verified
June 1, 2010
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GK-63
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.