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Clinical Trials/NCT02405299
NCT02405299
Completed
Not Applicable

Evaluation Des rééducations Neuropsychologiques Des Troubles de l'Inhibition Chez l'Enfant Avec un TDAH

L'hôpital Nord-Ouest - Villefranche Villefranche sur Saône1 site in 1 country60 target enrollmentOctober 2013
ConditionsADHD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
ADHD
Sponsor
L'hôpital Nord-Ouest - Villefranche Villefranche sur Saône
Enrollment
60
Locations
1
Primary Endpoint
scores to neuropsychological testing inhibition before and after rehabilitation in experimental groupe
Status
Completed
Last Updated
last year

Overview

Brief Summary

This research aims to assess the cognitives rehabilitations in attention deficit disorder (ADHD) in children. the objective is to demonstrate what are the most relevant cognitive factors for rehabilitative to improve the inhibition of disorders in ADHD.

Detailed Description

This study examines the effect of neuropsychological rehabilitation on the disorder inhibtion in the child with ADHD. Sample includes 60 subjects aged 9-13 years with disorder of inhibition evalued with neuropsychological test. Neuropsychological rehabilitation protocol was developed and evaluated. This study use baseline and includes a control group and an experimental group. The type of cognitive procedure (up / down, or rehabilitative / metacognitive) is examined.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
December 2016
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
L'hôpital Nord-Ouest - Villefranche Villefranche sur Saône
Responsible Party
Principal Investigator
Principal Investigator

Coline Perrier

Ms. Seguin Charlotte, neuropsychologist psychologist

L'hôpital Nord-Ouest - Villefranche Villefranche sur Saône

Eligibility Criteria

Inclusion Criteria

  • presence of a disorder of inhibition (assessed by neuropsychological subtests) as part of an ADHD with normal intellectual potential (ICV WISC4) in children born at term or preterm (-33SA)

Exclusion Criteria

  • patient refusal and family to participate in the study
  • subjects with sensory disorders, psychological or unsupported, subjects carrying other cognitive disorders prevalent disorder of inhibition
  • subjects with psychostimulant treatment at inclusion in the study

Outcomes

Primary Outcomes

scores to neuropsychological testing inhibition before and after rehabilitation in experimental groupe

Time Frame: 5 months

comparison of the results obtained by the experimental subjects neuropsychological tests before and after rehabilitation (standard notes to NEPSY subtests, TAP, TEA-ch, Stroop test)

Secondary Outcomes

  • scores to neuropsychological testing inhibition before and after rehabilitation in control group(5 months)

Study Sites (1)

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