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Clinical Trials/NCT00692796
NCT00692796
Completed
N/A

Pulmonary Rehabilitation for Idiopathic Pulmonary Fibrosis

National Jewish Health1 site in 1 country60 target enrollmentApril 2008

Overview

Phase
N/A
Intervention
Not specified
Conditions
Idiopathic Pulmonary Fibrosis
Sponsor
National Jewish Health
Enrollment
60
Locations
1
Primary Endpoint
Exercise capacity
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to determine the effects of Pulmonary Rehabilitation (PR) on shortness of breath, exercise capacity, symptom control, mental health, cognitive function, and quality of life in patients with Idiopathic Pulmonary Fibrosis (IPF). Pulmonary rehabilitation has already been shown to benefit patients with other chronic respiratory diseases, such as chronic obstructive pulmonary disease (COPD). We believe that pulmonary rehabilitation will benefit patients with IPF as well.

Detailed Description

The goals of this project are to assess the effect of PR on a number of important outcomes in patients with IPF. Once enrolled in the study, subjects will complete a battery of questionnaires and tests that assess symptoms, quality of life, cognition, and mental health, and then subjects will complete a six week outpatient PR program (at National Jewish Medical and Research Center or other PR programs). Subjects will complete the same battery of questionnaires and tests immediately after completion of the PR program and again six months later.

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
March 2010
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age 40 years or older
  • Diagnosis of IPF according to American Thoracic Society criteria
  • Exclusion criteria:
  • Patients who have completed a PR program within the last two years
  • Patients with unstable medical conditions that would make PR unsafe

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Exercise capacity

Time Frame: 6 weeks and again at 6 months

Secondary Outcomes

  • Anxiety(6 weeks and again at 6 months)
  • Depression(6 weeks and again at 6 months)
  • Cognition(6 weeks and again at 6 months)
  • Quality of life(6 weeks and again at 6 months)
  • Fatigue(6 weeks and again at 6 months)

Study Sites (1)

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