NCT07413419Not yet recruiting
Evaluation of Remote Motivational Interviewing for Disease Management in Heart Failure Patients and Their Carers
REMIND HF - Evaluation of Remote Motivational Interviewing for Disease Management in Heart Failure Patients and Their Carers
Source: ClinicalTrials.gov · Last updated 17 Feb 2026
Brief summary (registry, in English)
Heart failure (HF) is a chronic and progressive condition that significantly affects patients' quality of life and increases the burden on family caregivers. Many patients struggle with self-care, including medication adherence, diet, and symptom monitoring. The REMIND HF (REmote Motivational INterviewing for Disease Management in Heart Failure) study aims to evaluate the effectiveness of remote motivational interviewing (MI) as a behavioral intervention to improve disease management and self-care among heart failure patients and their informal caregivers. The intervention consists of a series of online motivational interviews conducted by trained nurses over a 12-month period, focusing on lifestyle modification, self-monitoring, and patient-caregiver cooperation. The study will be conducted at the Wroclaw Medical University and collaborating centers. It will enroll 300 patients with heart failure (The New York Heart Association Functional Classificaion - NYHA class: II-IV) and their primary caregivers. Outcomes will include self-care behaviors, quality of life, psychological well-being, and health service utilization. The results will contribute to developing accessible, patient-centered models of heart failure management based on telehealth and behavioral support.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 600 (estimated)
- First submitted
- 22 Jan 2026
- Start date
- 28 Feb 2026
- Primary completion date
- 31 Dec 2027
- Lead sponsor
- Wroclaw Medical University
- Diseases
- Heart failure
- NCT number
- NCT07413419
What you commit to
- Study type: Interventional
- Planned participants: 600
- From 28 Feb 2026 to the primary completion date, 31 Dec 2027
- 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
- Severe cognitive impairment that would limit the ability to participate in the intervention or complete study assessments.
- Acute coronary syndrome or other acute cardiac event within the last 3 months.
Other
- Residence in a nursing home or long-term care facility.
- Inability to participate in videoconferencing sessions.
- Participation in another interventional study that could interfere with the outcomes of this trial.
Who the study is looking for
- Adult patients aged 18 years or older.
- Diagnosis of heart failure.
- New York Heart Association (NYHA) functional class II-IV.
- Poor self-care as assessed at baseline.
- Receiving care at the participating heart failure clinic.
- Access to the internet and a device capable of videoconferencing.
- Ability to understand the study procedures and provide written informed consent.
- Having an identified primary informal caregiver willing to participate in the study.
- Informal caregivers aged 18 years or older.
- Caregivers identified by the patient as the primary person providing unpaid support in daily disease management.
- Caregivers able to understand the study procedures and provide written informed consent.
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 |
|---|---|---|---|
| University Clinical Hospital in Wroclaw Coordinator of this site? Confirm its status | Wroclaw | Poland | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.