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Clinical Trials in Turkey / NCT07538596
Starting soon Not applicable

Medication Training Via Ignite Based on Roy Model in Heart Failure: Medication Adherence and Symptom Management

NCT07538596 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-04-15
Last updated
2026-04-20

Condition(s) studied

Hearth Failure With Reduced Ejection Fraction (HFrEF)

Investigational drug(s) / intervention(s)

Ignite-Based Medication Management Training

Ignite-Based Medication Management Training: The intervention is a structured medication management training program based on the Roy Adaptation Model. It is delivered using an Ignite digital presentation format and sent to participants via WhatsApp. The content is developed using current evidence-based heart failure guidelines (AHA and ESC) and focuses on improving patients' adaptation to illness through four adaptive modes (physiological, self-concept, role function, and interdependence). Participants receive the training after discharge and are followed up at 4 and 12 weeks using standardized symptom and medication adherence scales.

Study summary

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

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Must be 18 years of age or older. * Individuals who are willing to participate in the study * No communication problems * Having been diagnosed with KY for at least 6 months * Having the ability to read, write and speak Turkish . * Mildly reduced ejection fraction (left ventricular EF 41-49%) * Individuals with WhatsApp application * Individuals who can use a smartphone Exclusion Criteria: * Not being willing to participate in the study don't be under the age of 18 * Lack of ability to read, write and speak Turkish * Low ejection fraction (left ventricle EF. 40%) * Preserved ejection fraction (left ventricular EF.50%)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Suleyman Yalcin City Hospital Istanbul Kadikoy

More Saglik Bilimleri Universitesi trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07538596 on ClinicalTrials.gov ↗ ← All trials in Turkey