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Can a team of specialists boost quality of life for heart pump patients?

NCT ID NCT05388019

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 adding a team of specialists—physical therapy, occupational therapy, palliative care, and social work—to standard clinic visits helps people with a ventricular assist device (VAD) feel better and function better. About 110 participants, including newly implanted and long-term VAD patients, will undergo exercise tests and fill out quality-of-life surveys. The goal is to see if this team approach reduces complications and hospital readmissions while improving daily life.

What this could mean

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

Active substance
multidisciplinary team clinic (physical therapy, occupational therapy, palliative care, social work) plus exercise tests and questionnaires
What this could lead to
If it works, this could show that adding a team of specialists to standard VAD care improves patients' quality of life and physical function.
What could go wrong
This is a small pilot study with no control group for the main comparison, so results may not be conclusive or apply to all VAD patients.

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 110 people

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

Started

Apr 2022

Expected to finish

May 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 for Group A (newly-implanted): * Ages 18+ * Individuals with ventricular assist device (VAD) implanted * Individuals who have not previously attended standard-of-care VAD follow-up clinic visits Exclusion Criteria for Group A: * Inability to answer quality of life questionnaires * Inability to perform the 6-minute walk test and Cardiopulmonary Exercise Test (CPET) * Individuals who have previously attended standard-of-care VAD follow-up clinic visits Inclusion Criteria for Group B (previously-implanted): * Ages 18+ * Individuals with ventricular assist device (VAD) implanted * Individuals who have previously attended standard-of-care VAD follow-up clinic visits Exclusion Criteria for Group B: * Inability to answer quality of life questionnaires * Inability to perform the 6-minute walk test and CPET

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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.

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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

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  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

  • Massachusetts General Hospital

    Boston, Massachusetts, 02114, United States

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