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Home workouts via video call may ease breathing in lung hypertension patients

NCT ID NCT07535398

Symptom relief Sponsor: Marmara University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Updated 1 time

Summary

This study tests whether supervised exercise sessions done at home through video calls can improve breathing, fatigue, and quality of life in people with elevated pulmonary artery pressure. Twelve adults with stable symptoms will be randomly assigned to either telerehabilitation or breathing exercises for 8 weeks. Researchers will measure changes in exercise capacity and symptom severity before and after the program.

What this could mean

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

Active substance
synchronous telerehabilitation (supervised exercise via videoconferencing)
What this could lead to
If it works, this could offer a convenient home-based option to improve exercise capacity and reduce breathlessness in people with elevated pulmonary artery pressure.
What could go wrong
This is a very small early trial with only 12 participants, so results may not apply to everyone. The intervention is short-term (8 weeks) and may not produce lasting benefits.

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

About 12 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Aug 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 to 65 years

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: * Adults aged 18 to 65 years * Elevated pulmonary artery pressure identified by echocardiography, defined as systolic pulmonary artery pressure (sPAP) of 50 mmHg or higher * Clinically stable and receiving medical treatment under cardiology follow-up World Health Organization functional class I or II * New York Heart Association (NYHA) functional class I or II * Living with a caregiver, family member, or another person who can provide assistance if needed * Access to the internet and adequate visual, cognitive, and functional ability to participate in videoconference-based sessions * Willing to participate and able to provide informed consent Exclusion Criteria: * Requirement for oxygen therapy * Musculoskeletal problems limiting participation in exercise * Ongoing treatment for psychiatric or psychological disorders * Cognitive impairment based on Mini-Mental State Examination findings * Severe chronic obstructive pulmonary disease (COPD) * Other significant cardiac disease that may interfere with participation or assessment

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Conditions

The condition(s) this trial relates to.

pulmonary hypertension

As listed by the trial registrant

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

Elevated pulmonary artery pressure

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Tokat Gaziosmanpaşa University

    RECRUITING

    Tokat Province, Turkey (Türkiye)