Pulmonary Rehabilitation in Patients With Sarcoidosis
NCT02044939 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 38
Last updated 2026-04-07
Summary
The primary objective of the study is to assess the improvement of daily activity in subjects with Stage IV Pulmonary Sarcoidosis one year after the conduct of a pulmonary rehabilitation program.
The secondary objectives are the following:
* assess the improvement of daily activity at several times : 2, 6 and 12 months after the beginning of a pulmonary rehabilitation program
* assess the improvement of exercise capacity by tests used in medical practice
* assess the correlation between daily activity and exercise capacity
* assess the improvement of dyspnea
* assess the improvement of quality of life and psychological state
Conditions
- Stage 4 Pulmonary Sarcoidosis
Interventions
- OTHER
-
Pulmonary rehabilitation program
Pulmonary rehabilitation program should follow ATS/ERS Guidelines (2006)
Sponsors & Collaborators
-
University Hospital, Lille
lead OTHER
Principal Investigators
-
Benoît WALLAERT, MD PhD · Clinique des Maladies Respiratoires, CHRU de Lille
-
Frédéric BART, MD · Service de Pneumologie, CH Béthune
-
Dominique VALEYRE, MD PhD · Service de pneumologie, Hôpital Avicenne AP-HP
-
Dominique ISRAEL-BIET, MD PhD · Service de Pneumologie, Hôpital européen Georges Pompidou. AP-HP
-
Jean AMOURETTE, MD · Service de Pneumologie, CH Arras
-
Yves PACHECO, MD PhD · Centre Hospitalier Lyon Sud
-
Vincent COTTIN, MD PhD · Service de Pneumologie, Hôpital Louis Pradel, Lyon
-
Martine REYNAUD-GAUBERT, MD PhD · CHU Nord, APHM Marseille
-
Sylvie LEROY, MD · Service de Pneumologie, Hôpital Pasteur - Pavillon H, CHU de Nice
-
Gaëtan DESLEE, MD · Hôpital Maison Blanche, CHU de Reims
-
François STEENHOUWER, MD · Service de Pneumologie, Hôpital Victor Provo, Roubaix
-
Alain DIDIER, MD · Clinique des Voies Respiratoires, Hôpital Larrey, Toulouse
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-07-10
- Primary Completion
- 2017-07-06
- Completion
- 2017-07-06
Countries
- France
Study Locations
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