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Heart pump patients to test Smartwatch-Guided home workouts

NCT ID NCT07611188

Symptom relief Sponsor: Puerta de Hierro University Hospital Source: ClinicalTrials.gov ↗

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a 12-week home exercise program, guided by a mobile app and smartwatch, can improve exercise capacity and quality of life in people with a left ventricular assist device (LVAD). About 78 participants who recently got an LVAD and cannot attend hospital rehab will be randomly assigned to either the home exercise program or usual care. The study will measure walking distance, safety, and emotional well-being.

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 78 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Dec 2030

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 (must meet all): * Recent LVAD Implantation (\<6 months) * Clinical stability (defined as meeting all of the following criteria): discharge from the LVAD implantation hospitalization, absence of inotropic medication, hemoglobin \>9 g/dL, and no active infection. * Inability to participate in a supervised rehabilitation program (due to lack of availability, or inability because geographical reasons). Exclusion Criteria (any): * Functional Inability to Perform Cardiopulmonary Exercise Testing * Prior Participation in a Supervised Rehabilitation Program (after the LVAD implantation)

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Conditions

The condition(s) this trial relates to.

advanced heart failure heart failure

As listed by the trial registrant

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

Advanced heart failure Cardiac rehabilitation Cardiopulmonary exercise test Conditioning therapy Exercise training Heart failure Left ventricular assist device LVAD Quality of life Remote exercise Six-minute walk test Telemedicine Telerehabilitation Ventricular assist device

How to take part

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

  1. The places running it

    10 sites. 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

  • Complejo Hospitalario Universitario Santiago de Compostela

    Santiago de Compostela, Galicia, 15706, Spain

  • Complejo Hospitalario Universitario de A Coruña

    A Coruña, Galicia, 15006, Spain

  • Hospital 12 de Octubre

    Madrid, Madrid, 28041, Spain

  • Hospital Clinic de Barcelona

    Barcelona, Catalonia, 03036, Spain

  • Hospital Clinico San Carlos

    Madrid, Madrid, 28040, Spain

  • Hospital Puerta de Hierro

    Majadahonda, Madrid, 28028, Spain

  • Hospital Ramon y Cajal

    Madrid, Madrid, 28034, Spain

  • Hospital Universitari de Bellvitge

    Barcelona, Catalonia, Spain

  • Hospital Universitario de Salamanca

    Salamanca, Castille and León, 37007, Spain

  • Hospital Virgen del Rocío

    Seville, Andalusia, 41013, Spain

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