The Value of a Simple Tool for the Early Detection of Decompensated Heart Failure in People Over 55 on Réunion Island: A Preliminary Study in Hospitals (DEPIST'IC-RUN)

ConditionHeart Failure
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age55+
SponsorCentre Hospitalier Universitaire de la Réunion

About this trial

The goal of this study is to assess the discriminatory power of a previously developed tool for detecting decompensated heart failure-which includes, in particular, clinical signs-in a population of patients hospitalized in cardiology units in Réunion. The main question it aims to answer is : Would a simple and rapid screening tool for decompensated heart failure help identify a high probability of this condition in a population hospitalized in a cardiology unit in Réunion? This study includes patients aged 55 and older, who reside in Réunion, who were admitted on an unscheduled basis to the cardiology department at the Réunion University Hospital or the Ouest Réunion Hospital, for any reason (whether as an inpatient or in the intensive care unit)

The study is conducted in two phases:

Phase 1: Development of the new e-DELPHI consensus-based screening tool Phase 2: Administration of the Déspist'IC-Run early detection tool for decompensated heart failure and performance of the gold standard cardiology examination (RIPH3)

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 55 and older

Admitted on an unscheduled basis to the cardiology department at the CHU (North and South campuses) and the CHOR for any reason (in general wards or intensive care)

Residents of Réunion

Able to read and write French

Disqualifiers

Who cannot communicate in French

For whom it is impossible to administer the questionnaire

For whom the ETT and/or cardiology consultation are impossible

Who are under guardianship, conservatorship, or judicial protection

Trial population

Patients aged 55 or older who reside on Réunion Island and are hospitalized in the cardiology department of the University Hospital (CHU) or the Centre Hospitalier Ouest Réunion (CHOR)

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Early Detection Questionnaire

    Diagnostic test

    Questionnaire for the Early Detection of Heart Failure

Treatment groups

300 Participants
are divided into 1 treatment group
Group A: Cardiology patients1 intervention

Trial outcomes

Primary outcomes

1

Estimating the discriminant validity of a tool for detecting decompensated heart failure

The probability of having decompensated heart failure, as determined by a screening tool in the form of a questionnaire, will be calculated using the equation of a logistic regression model that explains the observed status (dependent variable) as determined by the gold standard test. The gold standard test for establishing a definitive diagnosis of decompensated heart failure will combine three tests: a clinical examination by a cardiologist, a transthoracic Doppler echocardiogram (TTE), and an electrocardiogram.

Time frame
"From enrollment to the end of the study, at 6 month

Secondary outcomes

1

Describe the operational phases involved in developing the screening tool.

The detailed description of the tool's development phase is a task that complements statistical modeling (of the tool's development) and is purely epidemiological in nature.

Time frame
From enrolment to the end of the study, at 6 month
2

Describe the sociodemographic and clinical characteristics, as well as the lifestyle habits, of the study population.

The following characteristics are collected: age, sex, socioeconomic status, residential area (north, south, west, east); cardiovascular risk factors (hypertension, diabetes, dyslipidemia, known heart disease, history of myocardial infarction, end-stage renal disease requiring dialysis); lifestyle factors (Body Mass Index (kg/m²), physical activity \> 30 min at least 3 times/week, current smoking, alcohol consumption \> 3 drinks/day).

Time frame
From enrollment to the end of the study at 6 months
3

Compare the sociodemographic and medical characteristics of this population of patients hospitalized in cardiology with those of other populations of patients with heart failure seen in private practices-whether in cardiology or general practice

Socio-demographic data (age, sex, residential area) and clinical data (cardiovascular history) for the population with heart failure in Réunion, obtained from the SNDS, will be compared with those of the sample in this study

Time frame
From enrollment to the end of the study at 6 month

Other outcomes

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