Clinical Trials Directory

Trials / Completed

CompletedNCT04120857

A Tele-Health Symptom Management Program for Patients With Heart Failure: Pall-Heart

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
University of Virginia · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

Heart failure is common in adults and is the most common hospital diagnosis in older adults. Patients with heart failure suffer numerous distressing symptoms daily. Although palliative care can improve suffering, rural-dwelling heart failure patients have poor access to specialized palliative care. The investigators propose to pilot test a tele-health palliative care intervention, PALL-HEART, in rural dwelling heart failure patients who live in Virginia and Kentucky. Study specific objectives are: Primary Aims: * AIM 1: Compare HF patients who participate in a home-delivered tablet-based HF health education and gentle stretching intervention, to a health education (HE) group on: a) HF symptoms (weight gain, breathlessness, fatigue), b) psychological symptoms (depression, diminished QOL, resilience, self-care, and heart rate variability), c) physical function (endurance, strength, balance), and d) health care utilization rates (ED visits, office visits, hospitalizations). * Hypothesis 1: HF symptoms (weight gain, breathlessness, fatigue), psychological symptoms (depression, diminished QOL, resilience, self-care), physical function (endurance, strength, balance) will improve in the intervention group. * Hypothesis 2: Health care utilization rates (ED visits, office visits, hospitalizations) will decrease in the intervention group. Secondary: * AIM 2: Acceptability - Acceptability of the intervention will be determined using: a) participation and satisfaction rates (participant logs), b) intervention retention rates, and c) barriers to participation (technology and participant motivation issues). * Hypothesis: Subjects in the intervention group will have \>80% participation and satisfaction rates and be willing to identify barriers to participation. acceptability of the intervention for future refinement and large scale testing.

Conditions

Interventions

TypeNameDescription
BEHAVIORALGentle Stretching60 minutes fo gentle stretching twice weekly for 8 weeks

Timeline

Start date
2019-06-01
Primary completion
2020-09-30
Completion
2020-09-30
First posted
2019-10-09
Last updated
2020-11-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04120857. Inclusion in this directory is not an endorsement.