NCT00419289

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P75+ for not_applicable chronic-obstructive-pulmonary-disease

Timeline
Completed

Started Jan 2007

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2007

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

January 4, 2007

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 8, 2007

Completed
1.4 years until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2008

Completed
Last Updated

January 8, 2007

Status Verified

January 1, 2007

First QC Date

January 4, 2007

Last Update Submit

January 4, 2007

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

COPD, rehabilitation, quality of life

Outcome Measures

Primary Outcomes (2)

  • Disease specific Quality of Life

  • Work Capacity

Secondary Outcomes (1)

  • Number of days admitted to hospital

Interventions

follow-up rehabilitation of participants with COPDBEHAVIORAL

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • FEV1 \< 60% of expected

You may not qualify if:

  • Other severe chronic conditions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Internal Medicine M, Glostrup University Hospital

Copenhagen, Copenhagen, 2600, Denmark

Location

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Susanne Vest, MD

    Glostrup University Hospital, Copenhagen

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Susanne Vest, MD

CONTACT

susanne.vest@dadlnet.dk

Allan Linneberg, MD

CONTACT

alli@glostruphosp.kbhamt.dk

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

January 4, 2007

First Posted

January 8, 2007

Study Start

January 1, 2007

Study Completion

June 1, 2008

Last Updated

January 8, 2007

Record last verified: 2007-01

Locations

DK(1)