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Clinical Trials in France / NCT07570628
Starting soon Observational

Implementation of a Clinical Decision Support System in Primary Care for the Screening and Assessment of Frailty in Patients Aged 65 and Over

NCT07570628 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2027-01-02
Last updated
2026-05-13

Condition(s) studied

Frailty at Older AdultsPrimary CareGeriatric AssessmentImplementation ResearchInterprofessional Collaboration

Study summary

This observational study aims to evaluate the real-life use of a digital tool (Fragiclic) by general practitioners (GPs) and nurses to screen and assess frailty in adults aged 65 and over. Frailty is a syndrome that increases the risk of loss of autonomy, falls, hospitalizations, or death. The tool includes simple screening questionnaires (such as SEGAm) and a comprehensive assessment (CGA - Comprehensive Geriatric Assessment) to better manage patients' health.

The main question it aims to answer is:

* What proportion of patients aged 65 and over will benefit from frailty screening or assessment using Fragiclic over 12 months?

A secondary question is

\- Does the use of Fragiclic reduce the risk of unplanned hospitalizations or death in these patients?

For the secondary question, researchers will compare patients who received screening or assessment (with or without a Personalized Care Plan (PCP)) to those who did not, to determine if Fragiclic improves their health outcomes.

Participants will not have additional tasks: Their GP or nurse will use Fragiclic during routine consultations. Some patients may be asked to provide information about their health or quality of life (via their healthcare provider).

All data will be collected anonymously and securely

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Patients aged 65 years or older * Patient or trusted person who provided oral non-opposition after receiving full information about the protocol * Managed by the general practitioner if the patient or nurse during the study period. If patients are assessed by a nurse : Patients whose general practitioner is a participating physician in the study Exclusion Criteria: * Patients unable to express non-opposition or without a trusted person available to express non-opposition * Patients whose general practitioner (GP) is not a participating GP in the study * Patients or trusted persons who do not speak French

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
MSPU Torcy Torcy Rue Charlie-Chaplin

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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 NCT07570628 on ClinicalTrials.gov ↗ ← All trials in France