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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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07067047
Acronym
HF-DSS-Nursing
Enrollment
60
Registered
2025-07-15
Start date
2024-09-01
Completion date
2025-03-31
Last updated
2025-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Brief summary

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.

Interventions

BEHAVIORALNursing Decision Support System

A behavioral intervention involving a nurse-led decision support system designed to manage fluid volume overload in heart failure patients. The intervention guided nursing care planning, monitoring, and evaluation during hospitalization and through home follow-up visits.

Sponsors

Leyla Biçen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* Presence of additional comorbidities other than cardiac risk factors (e.g., dialysis-dependent renal failure, lymphedema, oncology patients, etc.) * Presence of severe valvular stenosis * History of amputation * Classified as morbidly obese * Isolated right heart failure * 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 * Development of poor general condition during follow-up * Transferred to intensive care units during follow-up * Extended hospitalization due to infection or other secondary causes

Design outcomes

Primary

MeasureTime frameDescription
Congestion Score ImprovementBaseline to 30 days post-dischargeAssessment of the reduction in fluid volume overload symptoms based on a standardized congestion scoring system. The score evaluates parameters such as edema, shortness of breath, and weight changes.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026