Emotions Analysis in Patients With Chronic Phase of Stroke Basal Ganglia

NCT ID: NCT02884882

Last Updated: 2018-11-28

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

TERMINATED

Clinical Phase

NA

Total Enrollment

149 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-12-31

Study Completion Date

2018-04-30

Brief Summary

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Compare the emotional experience of patients with focal lesions of the basal ganglia by ischemic or hemorrhagic damage and healthy participants. These anomalies will be highlighted by neuropsychological and electrophysiological assessments.

Detailed Description

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Conditions

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Stroke Basal Ganglia

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Emotional induction in stroke population

Six films are presented, each after a relaxation period after which the basal score is measured.

Group Type OTHER

Emotional induction

Intervention Type OTHER

Score (from 1 to 10) rated the felt for each target emotions for the following 6 dimensions: joy, sadness, fear, disgust, anger, no emotion, after the presentation of short sequences of standardized films.

Emotional induction in healthy volunteers

Six films are presented, each after a relaxation period after which the basal score is measured.

Group Type PLACEBO_COMPARATOR

Emotional induction

Intervention Type OTHER

Score (from 1 to 10) rated the felt for each target emotions for the following 6 dimensions: joy, sadness, fear, disgust, anger, no emotion, after the presentation of short sequences of standardized films.

Interventions

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Emotional induction

Score (from 1 to 10) rated the felt for each target emotions for the following 6 dimensions: joy, sadness, fear, disgust, anger, no emotion, after the presentation of short sequences of standardized films.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* For cases :

* right-handed patient
* ischemic or hemorrhagic stroke older than 3 months with single lesion preferably less than 20 mm in diameter affecting the basal ganglia and sparing cortex
* Rankin score estimated prior stroke must be equal to 0 and after stroke \<3 (at inclusion).
* For participants control : right-handed patient

Exclusion Criteria

* For cases : severe aphasia - Prosopagnosia apperceptive - cerebral neurological pathology associated history, especially dementia - History of depression and psychiatric disorders treated - another stroke vascular territory than that for which the patient is included - diffuse lesions of the white matter Fazekas a score of\> 2 (periventricular or subcortical) - Contraindications to MRI
* For participants control : No history neurosurgical - No history of head trauma with loss of consciousness - not known neurological disease - not known psychiatric illness - No psychotropic treatment
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Brest

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Serge TIMSIT

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Régional de Brest

Locations

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Centre Hospitalier Régional Universitaire de Brest

Brest, , France

Site Status

Countries

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France

Other Identifiers

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KALISS RB10.077

Identifier Type: -

Identifier Source: org_study_id

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