| NCT ID | NCT06988995 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Florida |
| Condition | LVAD Caregivers |
| Study Type | INTERVENTIONAL |
| Enrollment | 40 participants |
| Start Date | 2025-12-01 |
| Primary Completion | 2026-12 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 40 participants in total. It began in 2025-12-01 with a primary completion date of 2026-12.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Research has shown that LVAD patients and their caregivers typically experience increased mental health concerns and decreased quality of life following LVAD implantation and hospital discharge. The purpose of this study is to explore how to improve quality of life for LVAD patients and their caregivers in the initial transition from hospital to home after LVAD implantation. Over the course of the study, participants will complete 2 surveys: one when participants are in the hospital and one at a 2-month post-hospital follow-up appointment with the participants' cardiologist. Participants may be contacted if there is data missing from surveys. Participants may also be provided with information on improving mental health in the form of handouts or a brief meeting with a psychology provider.
Eligibility Criteria
Inclusion Criteria: * LVAD implantation or caregiver or patient with LVAD; over 18 years old; primary caregiver is a family member Exclusion Criteria: * Currently or in the past 3 months received psychotherapy or psychosocial or peer support; hospitalized for psychiatric reasons in the past 6 months; current, active suicidal thoughts or a reported suicide attempt within the past year; a current alcohol/substance use disorder that required immediate treatment; or a current or past thought disorder, psychosis, or unmanaged bipolar disorder; enrolled in another investigational research/clinical trial; toxic/negative dynamic between pt and caregiver; extended post-LVAD implantation course (i.e., more than 2 months in the hospital).
Frequently Asked Questions
Who can join the NCT06988995 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying LVAD Caregivers. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06988995 currently recruiting?
Yes, NCT06988995 is actively recruiting participants. Visit ClinicalTrials.gov or contact University of Florida to inquire about joining.
Where is the NCT06988995 trial being conducted?
This trial is being conducted at Gainesville, United States.
Who is sponsoring the NCT06988995 clinical trial?
NCT06988995 is sponsored by University of Florida. The trial plans to enroll 40 participants.