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Recruiting Observational

Development, Standardisation and Standardisation Project for a New Memory Assessment

NCT06564779 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2024-11-22
Last updated
2026-04-30

Condition(s) studied

Memory Disorders

Investigational drug(s) / intervention(s)

New memory assessment

New memory assessment: The intervention is part of the neuropsychological assessment carried out as part of routine care. It consists of carrying out the neuropsychological tests traditionally used to investigate the diagnostic hypothesis of Alzheimer's disease.

Study summary

Episodic memory (EM) is a neuropsychological marker of Alzheimer's disease (AD) (Thomas-Anterion, 2006). Current tests for its assessment do not take into account the identity and emotional aspects of memory (Van der Linden et al., 2018). However, there are models that integrate links with identity, self-awareness and experience. Pause et al. (2013) propose criteria to create ecological tools, including consideration of the emotional valence of memories and the spatio-temporal context of acquisition. In line with these criteria, we have developed a new tool: the NEM (New evaluation of Episodic Memory). Preliminary studies show different response profiles on the NEM among patients (Launay et al., 2023). We now want to evaluate the relevance of this tool in the differential diagnosis of AD.

Eligibility

Sex
ALL
Min age
50 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 50 years * Ability to understand judged sufficient by the assessor; * Amnesic MCI profile (Petersen, 2003) during the 1st medical consultation prior to the assessment being prescribed. Exclusion Criteria: * Severe auditory and/or visual sensory impairment not compatible with neuropsychological assessment; * Judged fit to take the test by the assessor; * Patient under guardianship, curatorship or family guardianship; * Opposition to data processing.

Primary outcome measure(s)

  • Score total NEM (new memory assessment) — baseline
    Sum of the episodic elements

Trial sites (1)

FacilityCityRegionStatus
University hospital Tours France Recruiting
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 NCT06564779 on ClinicalTrials.gov ↗ ← All trials in France