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Heart Failure Self-care Mobile Application to Reduce Readmissions Trial

Heart Failure Self-care Mobile Application to Reduce Readmissions Trial

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03982017
Acronym
HF-SMART
Enrollment
32
Registered
2019-06-11
Start date
2019-07-12
Completion date
2020-07-30
Last updated
2021-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

readmission, quality of life, self-care

Brief summary

This is a patient-centered comparative effectiveness feasibility pilot designed to examine an intervention to increase heart failure self-care and symptom recognition. The investigators will randomize 100 participants to receive either usual care at the time of discharge after heart failure admission or a smartphone application that enhances self-care.

Interventions

OTHERMobile Health Technology Platform

When the participant navigates to the program, s/he will follow the directions on how to use the program, sign the terms of agreement, put in a password and begin the welcome page. The participant will receive daily prompts to complete brief questionnaires and review specialized content.

OTHERUsual care

Routine care at the time of hospital discharge, to be provided at the discretion of the clinicians caring for the participant.

Sponsors

Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED
University of Pittsburgh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Inpatient admission for acute decompensated heart failure * Left ventricular systolic or diastolic heart failure * Owns a smartphone with a data plan

Exclusion criteria

* Hospice or life expectancy less than 6 months * Palliative inotrope use * Heart transplant listed, or status post transplant * Ventricular assist devise present, or awaiting placement * Not being discharged to home * Unable to provide consent or comply with the intervention * Current enrollment in a remote monitoring/ telehealth program

Design outcomes

Primary

MeasureTime frameDescription
Percent of participants readmitted within 30 days30 days post index discharge30-day readmission rate as determined by participant report or medical record query
Percent of participants readmitted within 90 days90 days post index discharge90-day readmission rate as determined by participant report or medical record query
Time to readmissionfrom the date of enrollment until the date of first documented admission or date of death from any cause, whichever comes first, assessed up to 90 daystime to readmission
Kansas City Cardiomyopathy Questionnaire at 30 days post enrollment30 days post index dischargeQuality of life, subjective level of function
Kansas City Cardiomyopathy Questionnaire at 90 days post enrollment90 days post index dischargeQuality of life, subjective level of function

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026