NCT07017751Completed
Pender HPM-Based Online Education and Telephone Follow-Up in Adults With Heart Failure
Effects of Pender's Health Promotion Model-Based Online Education and Telephone Follow-Up on Symptom Burden, Dietary Behaviors, and Medication Adherence in Adults With Heart Failure: A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 7 Oct 2026
Brief summary (registry, in English)
This randomized controlled trial evaluated the effects of Pender's Health Promotion Model (HPM)-based structured online education combined with planned telephone follow-up on heart failure symptom burden, heart failure-related dietary behaviors, and medication adherence among adults with heart failure. Sixty participants were randomly allocated in a 1:1 ratio to an intervention group or a control group. The intervention group received routine clinical care plus individualized synchronous online education and two planned telephone reinforcement contacts, whereas the control group received routine clinical care. The three primary outcomes were assessed at baseline and 2 months after baseline.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 60 (actual)
- First submitted
- 4 Jun 2025
- Start date
- 20 Dec 2025
- Primary completion date
- 15 Feb 2026
- Lead sponsor
- Naile ALANKAYA
- Diseases
- Heart failure
- NCT number
- NCT07017751
What you commit to
- Study type: Interventional
- Participants enrolled: 60
- From 20 Dec 2025 to the primary completion date, 15 Feb 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Having severe cognitive impairment or an active psychiatric illness that could interfere with participation in the study.
- Having severe visual, hearing, or speech impairment that could prevent effective communication and participation in the intervention.
- Being on a heart transplantation waiting list or having recently undergone heart transplantation and being under post-transplant follow-up.
Who the study is looking for
- Aged 18 years or older.
- Having a cardiologist-confirmed diagnosis of heart failure.
- Having access to the technological resources required for online participation (smartphone, tablet, or computer with internet access).
- Being literate and able to read, understand, and write in Turkish.
- Providing written informed consent to participate in the study.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Çanakkale Onsekiz Mart University, Faculty of Health Sciences Coordinator of this site? Confirm its status | Merkez | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.