Last updated: February 22, 2024
Sponsor: Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal
Overall Status: Completed
Phase
N/A
Condition
Speech Disorders
Neurologic Disorders
Memory Loss
Treatment
Identification of Graphic Markers
Clinical Study ID
NCT05537688
2023-1632
Ages > 50 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- = > 50 years old For control group :
- not have a diagnosis of minor or major neurocognitive disorder. For AD :
- Have mild stage Alzheimer's disease: 1/ Be diagnosed according to ICD-10 criteria forthe following conditions: Alzheimer's disease and 2/ Have an MMSE score between 20 and 27, corresponding to a major TNC of mild stage or have a diagnosis of minor TNC withan MMSE score between 25 and 30, the validity period of a previously done MMSE is 3months. For PPA :
- Have Primary Progressive Aphasia according to the Gorno-Tempini criteria (Gorno-Tempini et al., 2011) and have an MMSE score between 20 and 27, correspondingto major mild TNC or have a diagnosis of minor TNC with an MMSE score between 25 and 30, the validity period of a previously made MMSE is 3 months.
Exclusion
Exclusion Criteria:
- Presence of pathologies of the dominant upper limb(s) (left, right or ambidextrouslateralization) disabling such as osteoarthritis, finger amputation, etc.
- History of stroke.
- Illiterate person.
- Participate in a concurrent experimental clinical study, to avoid interference withour study.
- Not understand oral and written French. The speakers are French-speaking and thelanguage task is performed in French.
Study Design
Total Participants: 53
Treatment Group(s): 1
Primary Treatment: Identification of Graphic Markers
Phase:
Study Start date:
June 27, 2022
Estimated Completion Date:
August 27, 2023
Connect with a study center
CRIUGM
Montréal, Quebec H3W 1W5
CanadaSite Not Available

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