NCT05314686Completed
Telerehabilitation - Technical Validity and Clinical Feasibility
Technical Validity and Clinical Feasibility of Using a Telerehabilitation System Using Advanced Telehealth Technologies
Source: ClinicalTrials.gov · Last updated 4 Sept 2025
Brief summary (registry, in English)
This prospective study will be held in two steps. The aim of the first step is to assess the technical validity of transmitting data remotely from different devices connected to a telerehabilitation system. These will include real-time oximetry data during exercise on a cycle ergometer (heart rate and transcutaneous oxygen saturation) as well as daily step count from a commercially available physical activity tracker. The aim of the second step of the study is to assess the clinical feasibility of using the telerehabilitation system in real life conditions (in the home environment). Briefly, participants will benefit from a eight weeks pulmonary rehabilitation program performed at home, using the telerehabilitation system. Further details about the content of the program and the outcomes are provided below.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 40 (actual)
- First submitted
- 25 Mar 2022
- Start date
- 15 Nov 2022
- Primary completion date
- 31 Jul 2025
- Lead sponsor
- ADIR Association
- Diseases
- COPD
- NCT number
- NCT05314686
What you commit to
- Study type: Observational
- Participants enrolled: 40
- From 15 Nov 2022 to the primary completion date, 31 Jul 2025
- 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.
Other
- Consent withdrawal
Who the study is looking for
- Age superior to eighteen years.
- Stable (\> four weeks) chronic obstructive pulmonary disease, GOLD stage II to IV
- Referred to pulmonary rehabilitation (no contraindication to exercise training on a cycle ergometer).
- With or without oxygen during exercise.
- Specific inclusion criteria for the first step of the study:
- Able to perform forty-five minutes of exercise training on a cycle ergometer.
- Specific inclusion criteria for the second phase of the study:
- Person of legal age who may be present during home exercise sessions (relatives).
- Non-inclusion Criteria:
- Pregnancy or likely to be.
- Guardianship.
- Unable to consent.
- Referred to pulmonary rehabilitation before lung cancer surgery.
- Referred to pulmonary rehabilitation before lung volume reduction surgery scheduled in the next few months.
Age in the registry: 18 years to - · Sex: All
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| ADIR Association Coordinator of this site? Confirm its status | Bois-Guillaume | France | Unknown status |
Related publications
- Technical and clinical feasibility of a pulmonary telerehabilitation model for people with COPD.Arch Phys Med Rehabil · 2026 · PMID 42863686
This page is information, not medical advice. Discuss any trial with your doctor.