Can a team of specialists boost quality of life for heart pump patients?
NCT ID NCT05388019
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
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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
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About 110 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2022
- Expected to finish
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May 2026
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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.
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The places running it
1 site. The list below names each one and where it is.
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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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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
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Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
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