Development of the Effectiveness of Rehabilitation Tools for Neurovisual Disorders in Patients With Posterior Cortical Atrophy
NCT ID: NCT04041089
Last Updated: 2023-03-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
3 participants
INTERVENTIONAL
2019-09-02
2022-06-15
Brief Summary
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The present study thus has a double objective: the development of a complete tool to work on the recognition, localization and/or manipulation of objects; and the evaluation of the effectiveness of this type of management.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Recognition of objects
Patients will do the therapy in the following order: object location, object manipulation and object recognition
Recognition of objects
* Name of shapes / colors / images / objects
* Classification of shapes / colors / images / objects
Location of objects
Patients will do the therapy in the following order: object recognition, object location, and object manipulation
Location of objects
* Search for frequent/rarse targets among distractors sharing one or more characteristics with the target
* Hit/catch a stationary/mobile target as quickly as possible
Manipulation of objects
Patients will do the therapy in the following order: object manipulation, object recognition and object location
Manipulation of objects
* Storage of shapes/objects
* Use of everyday objects (pen, cutlery, etc.)
Interventions
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Recognition of objects
* Name of shapes / colors / images / objects
* Classification of shapes / colors / images / objects
Location of objects
* Search for frequent/rarse targets among distractors sharing one or more characteristics with the target
* Hit/catch a stationary/mobile target as quickly as possible
Manipulation of objects
* Storage of shapes/objects
* Use of everyday objects (pen, cutlery, etc.)
Eligibility Criteria
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Inclusion Criteria
* Male or Female
* Patients with a diagnosis of PCA according to the criteria of Tang-Wai et al (2004)
* MMS\>15
* Voluntary, written and informed consent of the patient himself or its legal representative (guardian/curator), with oral consent of the patient in all cases
* Anti-Alzheimer's and psychotropic treatments stable for one month, if taken by the patient
* Affiliation to a social security system
Exclusion Criteria
* Person under the protection of justice
* Pregnant women (a pregnancy test will be performed in premenopausal women)
50 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Nice
OTHER
Responsible Party
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Principal Investigators
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MOUTON Aurélie, Ph
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier Universitaire de Nice
Locations
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Institut Claude Pompidou - Centre Mémoire de Ressources et de Recherche du CHU de Nice
Nice, Alpes-Maritime, France
Countries
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Other Identifiers
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18-AOI-02
Identifier Type: -
Identifier Source: org_study_id
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