Palliative Care for Patients with Long-Term LVAD Support

This study is looking at whether a special type of care called palliative care can improve the health-related quality of life for people living with a Left Ventricular Assist Device (LVAD) for a long time. An LVAD is a mechanical pump that helps your heart pump blood. Palliative care focuses on providing comfort and support to patients and their families. This study will involve about 90 participants who are at least 18 years old and have had their LVAD for at least one year. You cannot join if you are listed for a heart transplant, are pregnant, or have received outpatient palliative care recently. The study will measure how many people join, how many stay in the study, and the use of medications related to palliative care over 6 months.

Study design
This is an interventional study planning to enroll 90 participants. It will test a palliative care intervention delivered by a specialist nurse.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed from enrollment to the end of the intervention at 6 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07445932

Palliative Care Intervention to Improve Health Related Quality of Life for Patients on Long-Term LVAD Support

Not Yet Recruiting
NAAges 18+InterventionalSupportive care
Medstar Health Research Institute
~90 participants
Updated 2026-03-03 on ClinicalTrials.gov
What's tested:Palliative care intervention

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Trial enrollment
Measured over From enrollment to end of intervention at 6 months
+7 more outcomes measured
Advanced Heart Failure
Mechanical Circulatory Support
Left Ventricular Assist Device
Palliative Care

NCT07445932

Where you'd take part

This study runs at 2 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Inova Schar Heart and Vascular Institute

    Fairfax, Virginiastudy coordinator listed

  • MedStar Washington Hospital Center

    Washington D.C., District of Columbiastudy coordinator listed

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Richa Gupta, MD · PRINCIPAL_INVESTIGATOR · Medstar Health Research Institute

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Eligibility criteria

Inclusion

LVAD patients \>= 18 years of age
\>= 1 year post-LVAD implantation

Exclusion

Listed for heart transplantation. Undergoing evaluation for heart transplantation, however, is not an exclusion.
Non-English speaking
Receiving outpatient palliative care in the last 6 months
Renal replacement therapy
Non-cardiac terminal illness
Women who are pregnant or planning to become pregnant
Inability to comply with study protocol and follow up
Inabilty to provide consent.
Cognitive impairment or intellectual disability that prohibits successful completion of the HRQoL scales or compliance with the study protocol and follow up.
  • Trial enrollmentFrom enrollment to end of intervention at 6 months

    Number of individuals consenting to enroll in the trial.

  • Intervention retentionFrom enrollment to end of intervention at 6 months

    Number of patients completing the 6 month intervention

  • Palliative care services - medicationsFrom enrollment to end of intervention at 6 months

    Number of supportive medications prescribed per patient

  • Palliative care services - referralsFrom enrollment to end of intervention at 6 months

    Number of referrals placed per patient to members of the palliative care interdisciplinary team, psychiatry/behavioral health, or cardiac rehab services. Rates of follow up to each referral placed.

  • Advance care planningFrom enrollment to end of intervention at 6 months

    We will track number of patients that have completed advance care planning

  • Patient satisfaction with interventionFrom enrollment to end of intervention at 6 months

    Survey scores (Likert scale)

  • Patient perspectives of interventionFrom enrollment to end of intervention at 6 months

    Themes/codes will be identified out of semi-structured interviews conducted with patients examining perspectives on and barriers/facilitators of the intervention. These will be quantified.

  • Provider perspectives of interventionFrom enrollment to end of intervention at 6 months

    Themes/codes will be identified out of semi-structured interviews conducted with providers examining perspectives on and barriers/facilitators of the intervention. These will be quantified.