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NCT Number: NCT07714460

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

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Pôle Santé Sarthe et Loir, La Flèche, Sarthe, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

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.

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.

Primary outcomes

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

    Time frame: 6-8 weeks after the intervention.

    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

Secondary outcomes

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

    Time frame: 6-8 weeks after the intervention.

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

    Time frame: 6-8 weeks after the intervention.

  3. 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).

    Time frame: 6-8 weeks after the intervention.

Study contacts

Contact information is provided by the study sponsor or research team.

Christelle JADEAU

CONTACT

[email protected]

+332 44 71 07 81

Cyrielle HOUALARD, MD

CONTACT

[email protected]

+332 43 43 43 43

Sponsors and collaborators

Lead sponsor

Centre Hospitalier le Mans

Other

Registry information

Official study title

Effect of Implementing Prevention Measures Through Personalized Information in Emergency Departments on Adherence to Prevention Measures: A Multicenter, Randomized Controlled Exploratory Trial

Acronym: PREV-URG

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Jul 20, 2026
Registry last updated
Jul 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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