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Recruiting NCT05717491

Study of Diabetes' Risk Factors and Accelerated Aging According to Socio-economic Status in a Population From the North of France

Conditions: Diabetes, PreDiabetes

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Enrollment: 2233
Sponsor: Institut Pasteur de Lille

Location: France

Summary

Populations in precarious situations or with low socio-economic status have an increased risk of diabetes and accelerated aging. According to the population studied, the elements that can explain these health inequalities are not unequivocal and remain poorly known.The north of France, particularly affected by socio-economic disparities, has a prevalence of diabetes among the highest in metropolitan France. This is why investigators want to study the clinical, biological, social and behavioural risk factors of the entry into diabetes and accelerated aging among a large population in the North of France.This study aims to characterize the population (among which a majority (55%) suffers from precarious conditions) who come to carry out their health examination at the Pasteur Institute in Lille in order to study the risk factors to better explain these health inequalities.This research consists of a main descriptive observational, cross-sectional study carried out on 2233 volunteers (main group) over 18 months, and a complementary analytical case-control study that will be offered to 216 participants (sub-group).

Eligibility Criteria

Inclusion Criteria:Adult, male or femaleConsultant for the health prevention examination at the Examination Centre of Health of the Institut Pasteur of LilleAvailable to follow the constraints generated by the studySignature of the informed consentStatus of insured person in FranceExclusion Criteria:Participation in another clinical study or in a period of exclusion from another studyAdult deprived of liberty or under judicial protectionImpediment to give the free and informed consent (understanding, persons under guardianship/curators, etc.)Incompatible schedulingOther reason (state of health or concomitant treatments,...) considered by the principal investigator or a qualified co-investigator not compatible with the proper conduct of the clinical study

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05717491). StuddyBuddy aggregates publicly available trial information.