Optimizing the Effect of COPD Rehabilitation
Primary Purpose
Chronic Obstructive Pulmonary Disease
Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
follow-up rehabilitation of participants with COPD
Sponsored by
About this trial
This is an interventional prevention trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD, rehabilitation, quality of life
Eligibility Criteria
Inclusion Criteria:
- FEV1 < 60% of expected
Exclusion Criteria:
- Other severe chronic conditions
Sites / Locations
- Department of Internal Medicine M, Glostrup University Hospital
Outcomes
Primary Outcome Measures
Disease specific Quality of Life
Work Capacity
Secondary Outcome Measures
Number of days admitted to hospital
Full Information
NCT ID
NCT00419289
First Posted
January 4, 2007
Last Updated
January 4, 2007
Sponsor
Glostrup University Hospital, Copenhagen
Collaborators
Ministry of the Interior and Health, Denmark
1. Study Identification
Unique Protocol Identification Number
NCT00419289
Brief Title
Optimizing the Effect of COPD Rehabilitation
Official Title
Rehabilitation of COPD Patients: Can the Effect be Prolonged by Follow-up and Continued Rehabilitation
Study Type
Interventional
2. Study Status
Record Verification Date
January 2007
Overall Recruitment Status
Unknown status
Study Start Date
January 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2008 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Glostrup University Hospital, Copenhagen
Collaborators
Ministry of the Interior and Health, Denmark
4. Oversight
5. Study Description
Brief Summary
Patients with Chronic Obstructive Pulmonary Disease (COPD) may benefit from an 8-week pulmonary rehabilitation programme. However, the effect of the programme tends to attenuate with time. Patients who complete the programme are randomized to continued rehabilitation follow-up and control follow-up.
Detailed Description
Patients with Chronic Obstructive Pulmonary Disease (COPD) may benefit from an 8-week pulmonary rehabilitation programme according to guidelines of the Danish Society of Pulmonary Medicine. However, the effect of programme tends to attenuate with time. Patients who complete the programme are randomized to continued rehabilitation follow-up and control follow-up.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
COPD, rehabilitation, quality of life
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (false)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
follow-up rehabilitation of participants with COPD
Primary Outcome Measure Information:
Title
Disease specific Quality of Life
Title
Work Capacity
Secondary Outcome Measure Information:
Title
Number of days admitted to hospital
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
FEV1 < 60% of expected
Exclusion Criteria:
Other severe chronic conditions
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Susanne Vest, MD
Email
susanne.vest@dadlnet.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Allan Linneberg, MD
Email
alli@glostruphosp.kbhamt.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susanne Vest, MD
Organizational Affiliation
Glostrup University Hospital, Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Internal Medicine M, Glostrup University Hospital
City
Copenhagen
ZIP/Postal Code
2600
Country
Denmark
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Susanne Vest, MD
Email
susanne.vest@dadlnet.dk
First Name & Middle Initial & Last Name & Degree
Susanne Vest, MD
12. IPD Sharing Statement
Learn more about this trial
Optimizing the Effect of COPD Rehabilitation
We'll reach out to this number within 24 hrs