Clinical Trials Directory

Trials / Completed

CompletedNCT05537688

Identification of Graphic Markers of Neurocognitive Disorders (MG)

Identification of Graphic Markers of Neurocognitive Disorders Such as Primary Progressive Aphasia (PPA) and Early-stage Alzheimer's Disease (AD) (MG)

Status
Completed
Phase
Study type
Observational
Enrollment
53 (actual)
Sponsor
Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal · Other Government
Sex
All
Age
50 Years
Healthy volunteers
Accepted

Summary

The diagnosis of neurocognitive disorders such as early Alzheimer's disease (AD) or primary progressive aphasia (PPA) is particularly difficult and constantly evolving, often leading to diagnostic erraticity. However, several studies have shown that graphic parameters are affected in people with moderate to severe Alzheimer's disease. The use of new technologies in the study and analysis of the abilities of people with neurodegenerative diseases is increasingly recommended. The use of a digital tablet with a stylus makes it possible to objectivize the kinematic parameters of writing (pressure, inclination, speed, jerk, time of writing task) and thus would allow a low-cost diffusion of this technology in particular by including it in already existing screening batteries. The overall objective of the project is to characterize and compare the graphical markers of a writing task, either language-based (writing words, non-words, sentences) or non-language-based (drawing shapes), in patients with PPA, early-stage Alzheimer's disease (i.e., at the stage of minor neurocognitive disorders and major neurocognitive disorders at the beginning of the disease), and in people with no cognitive disorders.

Conditions

Interventions

TypeNameDescription
BEHAVIORALIdentification of Graphic MarkersThe study consists of a single physical visit to the research team's site. Participants will take a graphic task included in a validated test for language impairment in adults and older adults (DTLA). This test with writing data has a maximum completion time of 15 minutes. Diagnostic data will be collected from the patient's chart, frailty data and socio-demographic data will be collected by self-questionnaires. Participants will be evaluated by the principal investigator or his or her representatives from the research team.

Timeline

Start date
2022-06-27
Primary completion
2023-06-27
Completion
2023-08-27
First posted
2022-09-13
Last updated
2024-02-23

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05537688. Inclusion in this directory is not an endorsement.