NCT05565872Completed
Effects of Supervision During a Community-based Exercise Intervention (Urban Training) in Patients With COPD
Effects of Face-to-face Versus Telematic Supervision During a Community-based Exercise Intervention (Urban Training) Plus Therapeutic Education Programme on Exercise Tolerance in Patients With Chronic Obstructive Pulmonary Disease
Source: ClinicalTrials.gov · Last updated 25 Nov 2024
Brief summary (registry, in English)
This project plans on a community-based exercise intervention (Urban Training) combined with therapeutic education program, by using public spaces and urban walkable trails, adapted to each patient needs and capabilities in patients with chronic obstructive pulmonary disease (COPD). The main objective of the present study is to evaluate the effects comparing different levels of supervision (face-to-face vs telematic) in the short-, medium- and long-term with respect to: (primary outcome): exercise capacity, and (secondary outcomes): physical activity, quality of life, mental health and COPD exacerbations.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 80 (actual)
- First submitted
- 27 Sept 2022
- Start date
- 5 Oct 2022
- Primary completion date
- 20 Jun 2024
- Lead sponsor
- Universidad Complutense de Madrid
- Diseases
- COPD
- NCT number
- NCT05565872
What you commit to
- Study type: Interventional
- Participants enrolled: 80
- From 5 Oct 2022 to the primary completion date, 20 Jun 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previous inclusion in a rehabilitation programme (previous 6 months)
Other illness
- Neuromuscular or neurological disorders and/or psychiatric or cognitive conditions that hindered they ability to cooperate
Other
- Comorbidity that could interfere with study intervention (e.g., severe orthopaedic problems)
Who the study is looking for
- age \> 18 years
- COPD diagnosed by pulmonary function tests during clinical stability, with a ratio of forced expiratory volume in one second (FEV1) to forced vital capacity (FVC) ≤ 0.70
- Clinical stability, defined as at least 6 weeks without COPD exacerbation
Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Zona Básica de Salud Torrejón de Ardoz Coordinator of this site? Confirm its status | Torrejón de Ardoz | Spain | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.