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Can a smartphone app keep COPD patients moving after rehab?

NCT ID NCT07262229

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jul 14, 2026 · Updated 2 times

Summary

This pilot study tests a mobile app called Respir'air BPCO designed to help people with COPD stay physically active after completing a pulmonary rehabilitation program. About 50 participants will either use the app plus usual care or just usual care alone. Researchers will check if the app is easy to use, acceptable, and whether it helps improve activity levels, self-management, and quality of life over 6 months.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

23 people

The number who actually took part.

Started

Jan 2026

Expected to finish

Nov 2026

An estimate. End dates often move.

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.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: 1. a GOLD COPD diagnosis stage 1 to 4, classification B or E; 2. admitted electively at Hospital for PR; 3. had completed the pulmonary rehabilitation program; 4. age over 18 years; 5. ability to provide informed consent; 6. internet access; 7. ownership of a smartphone or tablet; 8. self-assessed perceived ease of use of digital devices. Exclusion Criteria: 1. clinical instability confirmed by the team of healthcare professionals; 2. severe cardiovascular disease confirmed by medical diagnosis; 3. recent history of neoplasia or autoimmune disease; other physical activity-limiting clinical condition confirmed by medical diagnosis (e.g. neurological disease); 4. other respiratory disease as primary diagnosis; e) inability to read, understand or speak French; f) cognitive impairment diagnosed by the medical team.

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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

  • Pôle de pneumologie de l'Hôpital de Rolle

    Rolle, Switzerland

More trials for these conditions

Other studies related to the condition(s) this trial covers.