CEPPPIA Pilot. Experimental Center of Participative and Individualized Predictive Prevention in Auvergne

University Hospital, Clermont-Ferrand

Status: Completed

Conditions: Chronic Disease; Diabetes Mellitus; Obesity; Cardiovascular Diseases; Cancers

Treatments: Behavioral: online questionnaire

Study type: Interventional

Funder types: Other

Identifiers

NCT03378895

CHU-358

2017-A00666-47 (Other Identifier)

Details and patient eligibility

About

The state of health in France appears to be good with regard to major indicators such as life expectancy at birth.

However, France is characterized by a high standardized rate of premature mortality (deaths occurring before the age of 65) in comparison with other European countries, with geographical disparities. Between 2006 and 2010, the standardized rate of premature mortality was higher in Auvergne than the national average.

Chronic diseases such as cardiovascular diseases, cancers and / or metabolic diseases (including diabetes and obesity) are the main causes of these premature deaths. These diseases have several causes: they depend on the genetic heritage, the way of life and the environment. Family history is a known risk factor for these chronic diseases. Eating habits, insufficient physical activity or physical inactivity, excessive drinking and smoking which promote the occurrence of these chronic diseases are the main risk factors that we can modify. Preventive measures are known and are regularly the subject of public health plans and awareness campaigns targeting lifestyles modification of the populations. These prevention campaigns affect entire population, while the risk factors for chronic diseases are different from one to another, this encourages personalization of preventive measures. The CEPPPIA pilot study falls within this framework and aims to evaluate the feasibility of setting up an individualized prevention program on the modification of health behaviors among people aged 35 to 55, who has a moderate risk of developing chronic diseases and residing in Auvergne territory.

Full description

The state of health in France appears to be good with regard to major indicators such as life expectancy at birth.

However, France is characterized by a high standardized rate of premature mortality (deaths occurring before the age of 65) in comparison with other European countries, with geographical disparities. Between 2006 and 2010, the standardized rate of premature mortality was higher in Auvergne than the national average.

Chronic diseases such as cardiovascular diseases, cancers and / or metabolic diseases (including diabetes and obesity) are the main causes of these premature deaths. These diseases have several causes: they depend on the genetic heritage, the way of life and the environment. Family history is a known risk factor for these chronic diseases. Eating habits, insufficient physical activity or physical inactivity, excessive drinking and smoking which promote the occurrence of these chronic diseases are the main risk factors that we can modify. Preventive measures are known and are regularly the subject of public health plans and awareness campaigns targeting lifestyles modification of the populations. These prevention campaigns affect entire population, while the risk factors for chronic diseases are different from one to another, this encourages personalization of preventive measures. The CEPPPIA pilot study falls within this framework and aims to evaluate the feasibility of setting up an individualized prevention program on the modification of health behaviors among people aged 35 to 55, who has a moderate risk of developing chronic diseases and residing in Auvergne territory.

Enrollment: 251 patients

Sex: All

Ages: 35 to 55 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Men or women aged 35 to 55 years
• Subjects identified as moderate risk (group G1) following the assessment of the level of risk
• Covered by the Social Security
• Having signed the information form and having given his / her free consent during the inclusion visit
• Judged able to understand the aims of the study and ready to accept the constraints

Exclusion criteria

• Age <35 years or> 55 years
• Person who has not completed and validated the FSI (online health questionnaire)
• Person belonging to group G1 but with a moderate pathological risk (P1) and no identifiable risk in the behavioral field (C0)
• Pregnant or lactating women
• Persons benefiting from a legal protection measure
• Persons refusing to sign information and consent form
• Person in an exclusion period from another study, or having received more than 4500 € in the year
• Person deprived of his liberty by judicial or administrative decision
• Medical or surgical history, judged by the investigator to be incompatible with the study
• Suspicion of psychiatric disorders judged by the investigator to be incompatible with the study

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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251 participants in 1 patient group

adults aged 35 to 55 years

Experimental group

Treatment:

Behavioral: online questionnaire