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Active, not recruiting Not applicable

AZ@GAME-Eco: Economic Assessment of Serious Games for the Management of Alzheimer's Disease and Related Disorders

NCT03208491 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2017-09-30
Last updated
2026-06-15

Condition(s) studied

Alzheimer Disease

Investigational drug(s) / intervention(s)

serious games useusual care

serious games use: This program has enabled several SGs to be developed that allow physical and cognitive workouts to be carried out with a therapist

usual care: usual care of patient

Study summary

The main objective of AZ@GAME ECO is to evaluate the cost-utility of the management of patients suffering from Alzheimer's disease using a serious game providing cognitive and physical straining compared to a usual management. Among the secondary objectives it is important to assess the real life feasibility in different types of care structures.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Male or Female ≥ 60 years of age; * Subjects diagnosed with Alzheimer's Disease or related disorders associated with mild to moderately severe (CIM 10) * a score between 12 and 24 on the Mini Mental score evaluation * Subject treated in one of the participating centers * To have the social welfare insurance * Signature of the free and informed consent in the case of a patient under guardianship with signature of the guardian Exclusion Criteria: * history of epilepsy * major walking or balance disorder. * Subject without freedom by judicial or administrative decision

Primary outcome measure(s)

  • cost utility ratio — at 3 months
    Measurement of the incremental cost-utility ratio of the management of patients suffering from Alzheimer's disease

Trial sites (1)

FacilityCityRegionStatus
CHU de Nice Nice France
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 NCT03208491 on ClinicalTrials.gov ↗ ← All trials in France