Roy Model Medication Training Heart Failure Trial
Summary
NIH registered clinical trial NCT07538596 on ClinicalTrials.gov evaluating an Ignite-Based Medication Management Training program for heart failure patients. The trial will enroll participants with heart failure with reduced ejection fraction (HFrEF), randomizing them to receive structured medication training via WhatsApp or standard discharge education. Participants will be followed for 12 weeks with questionnaires at baseline, 4 weeks, and 12 weeks to assess medication adherence and symptom management outcomes.
What changed
NIH registered clinical trial NCT07538596, a randomized controlled study evaluating whether an Ignite-Based Medication Management Training program based on the Roy Adaptation Model improves medication adherence and heart failure symptoms compared to standard discharge education. Participants will receive training through WhatsApp after hospital discharge.
This registry entry does not impose compliance obligations. Sponsors and clinical investigators conducting similar heart failure medication adherence studies may reference this trial's design and endpoints for competitive benchmarking or protocol development, but no regulatory action is required.
Archived snapshot
Apr 21, 2026GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.
Medication Training Via Ignite Based on Roy Model in Heart Failure: Medication Adherence and Symptom Management
N/A NCT07538596 Kind: NA Apr 20, 2026
Abstract
The goal of this clinical trial is to learn if a structured medication training program can help people with heart failure better manage their condition. The program is based on the Roy Adaptation Model and is designed to support how people adjust to their illness.
The main questions it aims to answer are:
Does the training program improve heart failure symptoms? Does the training program help participants take their medications as prescribed?
Researchers will compare a training program group to a control group receiving standard care to see if the program is effective.
Participants will:
Be randomly assigned to either a training program group or a control group Receive the training program through WhatsApp after hospital discharge or receive standard discharge education Be followed for 12 weeks Complete questionnaires at the start of the study, at 4 weeks, and at 12 weeks
Conditions: Hearth Failure With Reduced Ejection Fraction (HFrEF)
Interventions: Ignite-Based Medication Management Training
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