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Assessment of Neurocognitive Rehabilitations of Inhibition of Disorders in ADHD in Children (ERNTITDAH)

L

L'hôpital Nord-Ouest - Villefranche Villefranche sur Saône

Status

Completed

Conditions

ADHD

Treatments

Other: experimental groupe

Study type

Interventional

Funder types

Other

Identifiers

NCT02405299
HNOVillefranche

Details and patient eligibility

About

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.

Full 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.

Enrollment

60 patients

Sex

All

Ages

9 to 13 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups, including a placebo group

Experimental Group
Experimental group
Description:
neuropsychological reeducation disorder specific of inhibition (bottom-up and top-down protocol): 24 bi-weekly sessions (30 subjects)
Treatment:
Other: experimental groupe
Control Group
Placebo Comparator group
Description:
non-specific and general cognitive neuropsychological reeducation (comprehension, syntactic, visuospatial) : 24 bi-weekly sessions (30 subjects)
Treatment:
Other: experimental groupe

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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