Condition: Chronic Obstructive Pulmonary Disease (COPD) · Sponsor: ADIR Association
Background and study aims: Chronic obstructive pulmonary disease is a leading cause of mortality worldwide. Pulmonary rehabilitation is recommended for patients to improve dyspnea, exercise capacity, and quality of life. Paradoxically, as few as 5 to 10% of eligible patients undergo pulmonary rehabilitation due to barriers such as transportation difficulties and limited availability of pulmonary rehabilitation centers. Home-based pulmonary rehabilitation using advanced telehealth technologies (telerehabilitation) may offer a solution to improve access. This study aims to compare the relative effectiveness of a home-based telerehabilitation program with center-based program. The primary objective is to assess changes in exercise endurance capacity, measured by endurance time, before and after participation of the rehabilitation program. Who can participate? Adults between 45 and 80 years old who are referred for pulmonary rehabilitation and have a confirmed diagnosis of chronic obstrucitve pulmonary disease (GOLD stage II to IV) at any of the participating centers are eligible to participate, whether or not they use oxygen during exercise. Participants must live at home with another adult who is present during exercise sessions. They must not have experienced any exacerbation in the month prior to study inclusion, nor have participated in a pulmonary rehabilitation program within the past year. Participants must not have any scheduled surgery within the next four months, i…
This description comes directly from the study's public registry record.
Tristan Bonnevie, PhD · 0235592970 · t.bonnevie@adir-hautenormandie.com
Always discuss trial participation with your own doctor first.
| Groupe Hospitalier du Havre | Montivilliers, France | Not Yet Recruiting |
| Centre Hospitalier des Pays de Morlaix | Morlaix, France | Not Yet Recruiting |
| Association ADIR | Rouen, France | Recruiting |
| Hôpital La Musse | Saint-Sébastien-de-Morsent, France | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT07025382