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NCT00419289 Clinical Trial

Optimizing the Effect of COPD Rehabilitation

Chronic Obstructive Pulmonary Disease Clinical Trial

Official title:
Rehabilitation of COPD Patients: Can the Effect be Prolonged by Follow-up and Continued Rehabilitation

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT00419289
Other study ID # KA20060179
Secondary ID
Status Not yet recruiting
Phase N/A
First received January 4, 2007
Last updated January 4, 2007
Start date January 2007
Est. completion date June 2008

Study information
Verified date January 2007
Source Glostrup University Hospital, Copenhagen
Contact Susanne Vest, MD
Email susanne.vest@dadlnet.dk
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 120
Est. completion date June 2008
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- FEV1 < 60% of expected

Exclusion Criteria:

- Other severe chronic conditions

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Behavioral:
• follow-up rehabilitation of participants with COPD

Locations
Country Name City State
Denmark Department of Internal Medicine M, Glostrup University Hospital Copenhagen

Sponsors (2)
Lead Sponsor Collaborator
Glostrup University Hospital, Copenhagen Ministry of the Interior and Health, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Disease specific Quality of Life
Primary Work Capacity
Secondary Number of days admitted to hospital
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