Assessment of Empathetic Process by Scanpath Study of an Artwork

NCT ID: NCT04665622

Last Updated: 2022-03-09

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-04-01

Study Completion Date

2019-12-31

Brief Summary

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Analysis of gaze patterns during social cognition tasks and standardised exploration of a specific artwork, between elderly subjects without cognitive disorders and subjects with neurodegenerative diseases such as Fronto-Temporal Dementia, Alzheimer's Dementia or Parkinson's Disease

Detailed Description

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Conditions

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Alzheimer Dementia Parkinson Disease Fronto-Temporal Dementia

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

A monocentric prospective, descriptive, comparative study.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Fronto-temporal Dementia

10 subjects

Group Type OTHER

Eye-Tracking / Neuropsychological evaluations

Intervention Type OTHER

Use of Eye-Tracking / Neuropsychological évaluations in 4 groups

Alzheimer's Dementia

20 subjects

Group Type OTHER

Eye-Tracking / Neuropsychological evaluations

Intervention Type OTHER

Use of Eye-Tracking / Neuropsychological évaluations in 4 groups

Parkinson's Disease

20 subjects

Group Type OTHER

Eye-Tracking / Neuropsychological evaluations

Intervention Type OTHER

Use of Eye-Tracking / Neuropsychological évaluations in 4 groups

Healthy volunteers

20 subjects

Group Type OTHER

Eye-Tracking / Neuropsychological evaluations

Intervention Type OTHER

Use of Eye-Tracking / Neuropsychological évaluations in 4 groups

Interventions

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Eye-Tracking / Neuropsychological evaluations

Use of Eye-Tracking / Neuropsychological évaluations in 4 groups

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Male or Female.
* 60 years old and above.
* Sufficient written and oral expression in French.
* Benefit from French or Monaco Social security.
* Written informed consent signed by the patient.
* For the control group: voluntary subjects, without cognitive impairment.
* For the FTD / AD / PD groups: patients diagnosed with one of these diseases, and volunteers to participate in the study.

Exclusion Criteria

* General anaesthesia within 3 months.
* Ophthalmological problems preventing a video-oculography examination.
* Oculomotor disorders such as "fixation disorders" or "ocular tracking disorders".
* History of stroke.
* Cognitive disorders of the type: visual agnosia, visuo-spatial disorder, visuo-perceptual disorder or aphasia.
Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Association de Recherche Bibliographique pour les Neurosciences

OTHER

Sponsor Role collaborator

Centre Hospitalier Princesse Grace

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centre Hospitalier Princesse Grace

Monaco, , Monaco

Site Status

Countries

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Monaco

Other Identifiers

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EYE-EMPATH

Identifier Type: -

Identifier Source: org_study_id

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