ADL- Training for Patients With Chronic Obstructive Pulmonary Disease (COPD)
Activities of Daily Living (ADL)-Training for Patients With Chronic Obstructive Pulmonary Disease (COPD)
1 other identifier
interventional
24
1 country
2
Brief Summary
ADL training of copd patients results in better execution of activities of daily living.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable chronic-obstructive-pulmonary-disease
Started May 2009
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 14, 2009
CompletedFirst Posted
Study publicly available on registry
April 24, 2009
CompletedStudy Start
First participant enrolled
May 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2010
CompletedJune 23, 2010
June 1, 2010
9 months
April 14, 2009
June 22, 2010
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Canadian Occupational Performance Measure(COPM) - Self-perception of occupational performance and satisfaction.
Baseline, 4 weeks; 3 months
Study Arms (2)
1: Standard rehabilitation programme
NO INTERVENTION2. Additional ADL training
EXPERIMENTALInterventions
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.
Eligibility Criteria
You may qualify if:
- COPD
- Referred for rehabilitation
- Age \> 18 years
- Symptoms affecting ADL function
- minute walk distance (6MWD) \< 400 meters
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- LHL Helselead
Study Sites (2)
Glittreklinikken
Hakadal, Akershus, 1485, Norway
Glittreklinikken
Hakadal, 1485, Norway
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Morten S Ryg, Dr philos
LHL Helse
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
April 14, 2009
First Posted
April 24, 2009
Study Start
May 1, 2009
Primary Completion
February 1, 2010
Study Completion
June 1, 2010
Last Updated
June 23, 2010
Record last verified: 2010-06