NCT07067047Completed
The Effect of Nursing Care Decision Support System Designed for Fluid Volume Excess of Patients With Heart Failure on Clinical Outcomes of Patients and Home Self-Care Outcomes
Source: ClinicalTrials.gov · Last updated 15 Jul 2025
Brief summary (registry, in English)
This study aims to evaluate the effects of a nursing care decision support system designed to reduce fluid overload in patients with heart failure. The goal is to examine its impact on clinical outcomes both during hospitalization and after discharge at home. The study focuses on improving nursing interventions and patient follow-up through structured, evidence-based decision-making tools.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 60 (actual)
- First submitted
- 4 Jul 2025
- Start date
- 1 Sept 2024
- Primary completion date
- 31 Mar 2025
- Lead sponsor
- Leyla Biçen
- Diseases
- Heart failure
- NCT number
- NCT07067047
What you commit to
- Study type: Interventional
- Participants enrolled: 60
- From 1 Sept 2024 to the primary completion date, 31 Mar 2025
- 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
- Presence of additional comorbidities other than cardiac risk factors (e.g., dialysis-dependent renal failure, lymphedema, oncology patients, etc.)
- History of amputation
- Isolated right heart failure
- Development of poor general condition during follow-up
- Extended hospitalization due to infection or other secondary causes
Other
- Presence of severe valvular stenosis
- Classified as morbidly obese
- Inadequate cooperation or communication skills
- Terminal stage patients
- Absence of echocardiographic evaluation
- BNP level not measured
- Criteria for Discontinuation During the Study:
- Inaccessible by phone
- Withdrawal of consent
- Transferred to intensive care units during follow-up
Who the study is looking for
- Diagnosed with heart failure (HF)
- Aged 18 years or older
- Ejection fraction below 50%
- Presence of +1 or greater pitting edema in the extremities
- Voluntary agreement to participate in the study
- Sufficient cognitive and communicative ability to participate in interviews and complete scales/forms
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 |
|---|---|---|---|
| İzmir Katip Çelebi University Atatürk Training and Research Hospital Coordinator of this site? Confirm its status | Izmir | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.