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Clinical Trials in France / NCT07714460
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Effect of Implementing Prevention Measures Through Personalized Information in Emergency Departments on Adherence to Prevention Measures

NCT07714460 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-07-27
Last updated
2026-07-22

Condition(s) studied

Prevention

Investigational drug(s) / intervention(s)

personalized preventive health informationnon-personalized preventive health information

personalized preventive health information: The intervention involves providing personalized preventive health information regarding recommended preventive measures based on age, biological sex, weight, height, bedtime and wake-up times, the presence of chronic conditions, and tobacco or alcohol use.

non-personalized preventive health information: The intervention involves providing non-personalized preventive health information. The patient receives all the preventive health information without it being tailored to the patient. The patient therefore does not see any information specific to him or her.

Study summary

Prevention, a cornerstone of public health, remains underutilized despite its proven effectiveness. Vaccinations, screenings, reduced consumption of toxic substances, and healthy lifestyle and dietary habits can significantly reduce morbidity and mortality. However, participation rates in France remain low compared to those of neighboring European countries, particularly with regard to cancer screenings and vaccination coverage. A lack of information, motivation, or unequal access hinders adherence to preventive measures. Some of these factors can be addressed.

Emergency departments, although rarely utilized for prevention, serve a diverse population and could serve as a strategic lever for educating the public about preventive health measures.

Personalized information, supported by a digital tool, could improve adherence to preventive measures. An interactive questionnaire was developed to tailor the information provided to patients based on their personal characteristics. The information delivered in this way would be more targeted for each patient and more likely to have a positive impact on the implementation of various preventive measures.

The purpose of this study is to determine whether a digital tool that provides personalized prevention information is more effective than general, non-personalized information in improving adherence among patients visiting the emergency department to the preventive measures recommended for them.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patients (≥ 18 years of age) * Patients seen in the emergency departments of Le Mans University Hospital and the PSSL * Patients who have given their free and informed oral consent Exclusion Criteria: * Patients who have previously participated in the study * Patients with limited understanding of the French language * Patients unable to give informed consent * Individuals not enrolled in or not eligible for a social security program * Individuals deprived of their liberty by judicial or administrative order * Individuals receiving involuntary psychiatric care * Individuals subject to a legal protective measure * Pregnant or breastfeeding patients.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Pôle Santé Sarthe et Loir La Flèche Sarthe
Centre Hospitalier du Mans Le Mans Sarthe

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07714460 on ClinicalTrials.gov ↗ ← All trials in France