Effect of Implementing Prevention Measures Through Personalized Information in Emergency Departments on Adherence to Prevention Measures

NCT07714460 | Not Yet Recruiting

• 1 other identifier: CHM-2025/S02/17
• Study Type: interventional
• Target: 658
• Locations: 1 country
• Sites: 2

Brief 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.

Conditions

Prevention

Keywords

personalized prevention

Outcome Measures

Primary Outcomes (1)

• proportion of patients who adhered to at least 25% of the preventive measures

  The primary outcome measure is the proportion of patients who adhered to at least 25% of the preventive measures for which they were eligible, as assessed 6-8 weeks after the intervention. Adherence is defined as the completion of a preventive measure or the initiation of steps leading to its completion in the short term

  6-8 weeks after the intervention.

Secondary Outcomes (3)

• The proportion of patients who adhered to each of the preventive measures studied.

  6-8 weeks after the intervention.

• The proportion of preventive measures taken by the patient, relative to the measures for which the patient is eligible.

  6-8 weeks after the intervention.

• The enrollment rate for each epidemiological subgroup (age, sex, whether the patient has a primary care physician, whether the patient has a chronic condition, socioeconomic status).

  6-8 weeks after the intervention.

Study Arms (2)

A - Intervention

EXPERIMENTAL

The first "intervention" group, designated A, is exposed to personalized information via a digital educational tool based on the characteristics entered for them.

Procedure: personalized preventive health information

B - Control

EXPERIMENTAL

The second "control" group, designated B, receives non-personalized information. Using the same digital tool, 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.

Procedure: non-personalized preventive health information

Interventions

non-personalized preventive health information PROCEDURE

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.

B - Control

personalized preventive health information PROCEDURE

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.

A - Intervention

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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

You may not qualify if:

• 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.

Sponsors & Collaborators

• Centre Hospitalier le Mans: lead

Study Sites (2)

Pôle Santé Sarthe et Loir

La Flèche, Sarthe, 72205, France

Location

Centre Hospitalier du Mans

Le Mans, Sarthe, 72000, France

Location

Central Study Contacts

Christelle JADEAU

CONTACT

+332 44 71 07 81; cjadeau@ch-lemans.fr

Cyrielle HOUALARD, MD

CONTACT

+332 43 43 43 43; choualard@ch-lemans.fr

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 15, 2026
• First Posted: July 20, 2026
• Study Start: July 27, 2026
• Primary Completion (Estimated): November 27, 2026
• Study Completion (Estimated): January 27, 2027
• Last Updated: July 22, 2026

Record last verified: 2026-07

Locations

FR (2)