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Can a home rehab system help COPD patients breathe easier?

NCT ID NCT05314686

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study tested whether a telerehabilitation system can reliably track heart rate, oxygen levels, and step counts in people with chronic obstructive pulmonary disease (COPD). In the first phase, 40 patients used the system during exercise sessions; in the second phase, they used it at home for eight weeks. The goal was to see if the technology works accurately and is practical for home use.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
telerehabilitation system (remote monitoring devices: pulse oximeter and physical activity tracker)
What this could lead to
If successful, this could pave the way for remote pulmonary rehabilitation programs for COPD patients, making care more accessible.
What could go wrong
This is a small, early feasibility study (40 participants) focused on technical performance, not health outcomes. The system may not work for all patients or in all home settings.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

40 people

The number who actually took part.

Started

Nov 2022

Finished

Aug 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Chronic obstructive pulmonary disease

Ages

18 years and older

Sex

Anyone

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * 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. Exclusion Criteria: * Consent withdrawal

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • ADIR Association

    Bois-Guillaume, ADIR Association, 76230, France

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