Pulmonary Rehabilitation
OtherStructured education and supervised exercise program, lasting between 6 and 9 weeks.
NCT Number: NCT01055730
The purpose of this study is to determine if pulmonary rehabilitation has any effect on breathlessness, quality of life, physical function and depression in persons with interstitial lung disease.
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Notify Me19 year and older
All sexes
Observational
University of British Columbia, Vancouver, British Columbia, Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Structured education and supervised exercise program, lasting between 6 and 9 weeks.
Time frame: Immediately following completion of pulmonary rehabilitation and 6 months following the start of pulmonary rehabilitation
Time frame: Immediately following completion of pulmonary rehabilitation and 6 months following the start of pulmonary rehabilitation
Time frame: Immediately following completion of pulmonary rehabilitation and 6 months following the start of pulmonary rehabilitation
Time frame: Immediately following completion of pulmonary rehabilitation and 6 months following the start of pulmonary rehabilitation
University of California, San Francisco
Other
The Impact of Pulmonary Rehabilitation in Interstitial Lung Disease: A Prospective Cohort Study
Acronym: PR-ILD
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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