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The Validity and Reliability of the Turkish Version of the Heart Failure Somatic Perception Scale

H

Hacettepe University

Status

Not yet enrolling

Conditions

Heart Failure

Study type

Observational

Funder types

Other

Identifiers

NCT06681714
SBA 24/702

Details and patient eligibility

About

The aim of this study is to evaluate The Validity and Reliability of the Turkish Version of the Heart Failure Somatic Perception Scale in patients with heart failure.

Full description

Heart failure is a global health issue that serves as the endpoint for many cardiovascular conditions, particularly coronary heart disease and hypertension. Common symptoms of heart failure include fatigue, dyspnea, edema, cough, lack of energy, orthopnea, paroxysmal nocturnal dyspnea, palpitations, and dizziness. These symptoms significantly affect the health-related quality of life of individuals with heart failure, especially in the palliative phase of the disease. Additionally, heart failure patients often experience physical limitations, reduced quality of life, and an increased rate of hospital admissions due to symptoms such as breathlessness and fatigue. The Heart Failure Somatic Perception Scale assesses the presence and severity of 18 common physical signs and symptoms of heart failure (e.g. chest pain), as well as dyspnea and its impact on daily activities through six items. Robust and rigorous measures are needed to assess the complexity of heart failure symptoms, and evidence suggests that evaluating a broad range of heart failure symptoms can be beneficial in guiding rehabilitation approaches, clinical decision-making, and survival prediction.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

A diagnosis of heart failure. Use of optimal pharmacological treatment according to current guidelines for at least 3 months.

Functional capacity classified as New York Heart Association (NYHA) Class I-IV (ambulatory).

Age 18 or older. Ability to cooperate with measurements.

Exclusion criteria

Known cognitive impairment. Having undergone acute coronary syndrome, percutaneous coronary intervention, or heart surgery within the past three months.

Trial design

100 participants in 1 patient group

Heart Failure
Description:
Patients with heart failure

Trial contacts and locations

1

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Central trial contact

Aynur Demirel, PT, PhD; Hidaye Yamikan, PT,MSc

Data sourced from clinicaltrials.gov

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