Study of the Prevalence of Diabetes and Pre-diabetes in Réunion Island

NCT ID: NCT06473584

Last Updated: 2025-07-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

2000 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-04-02

Study Completion Date

2026-12-31

Brief Summary

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In view of the new priority given to diabetes in Réunion and the implementation of an ambitious plan to combat the disease at regional level, which includes the identification and management of pre-diabetes, the need for up-to-date data on the extent of these 2 diseases (diabetes and pre-diabetes) has become essential.

These two diseases have known risk factors: age, overweight, obesity, high waist circumference, family history, hypertension, eating habits and physical activity, all of which form part of a risk score for developing diabetes: the Findrisk recommended by the Haute Autorité de Santé for identifying people at risk of diabetes. Given the specific population characteristics of Réunion compared with Finland, where this score has been validated, it would seem important to be able to measure these risk indicators in the population as a function of carbohydrate status in order to check that the proposed thresholds are appropriate for the population of Réunion.

Finally, cardiovascular risk has been described as early as the pre-diabetes stage. Given the young age of onset of diabetes in Réunion and the high proportion of diagnoses of diabetes made following the occurrence of a cardiovascular complication, the study of the prognosis of carbohydrate status on the occurrence of complications using the social security information system will be offered on a voluntary basis to study subjects (via a probabilistic social security link).

Detailed Description

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Conditions

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Diabetes

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Detection of glycaemic anomalies

Group Type OTHER

Diabetes detection

Intervention Type DIAGNOSTIC_TEST

Fasting glycemia on blood sample

Interventions

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Diabetes detection

Fasting glycemia on blood sample

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Have lived in Réunion island for at least one year
* Be aged between 18 and 75
* Affiliated to or benefiting from a social security scheme
* Free, informed and signed consent

Exclusion Criteria

* No main residence on the island or fixed address for at least one year on the island
* Participation in experimental research
* Pregnant women
* Adults under guardianship or legal protection
* Not understanding French
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Agence Régionale de Santé de La Réunion

UNKNOWN

Sponsor Role collaborator

Centre Hospitalier Universitaire de la Réunion

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Catherine MARIMOUTOU, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

CHU La Réunion

Locations

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CHU La Réunion

Saint-Denis, , Reunion

Site Status RECRUITING

Countries

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Reunion

Central Contacts

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Catherine MARIMOUTOU, MD, PhD

Role: CONTACT

+262 (0)262 90 50 50

Florence LEFEBVRE D'HELLENCOURT

Role: CONTACT

+262 262 75 34 71

Facility Contacts

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Catherine MARIMOUTOU, MD

Role: primary

262+ 262 90 50 27

Laetitia BERLY, PhD

Role: backup

Other Identifiers

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2023/CHU/42

Identifier Type: -

Identifier Source: org_study_id

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