Phase
Condition
Autism
Neuronal Ceroid Lipofuscinoses (Ncl)
Holoprosencephaly
Treatment
Proprioception and tactile localization with manual or ocular response and/or free hand grasp
Clinical Study ID
Ages 9-40 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male or female
Aged 9 to 11 or 18 to 40
Affiliated to a health care organism
Signed written informed consent (adult subjects)
One of the legal guardians of children subjects providing their free, informed andwritten consent to participate in the study; With the child also giving orally hisconsent to participate.
For participants with Developmental coordination disorder:
Subjects fulfilling the diagnostic criteria for dyspraxia of DSM-5 (these criteriawill be verified by the principal investigator)
Total MABC-2 score below the 15th percentile (if this MABC-2 assessment is alreadyavailable).
Exclusion
Exclusion Criteria:
Prematurity
Known neurological pathology (other than dyspraxia)
Intellectual disability
Visual impairment
Surgery or trauma to the upper limbs that has occurred too recently to allow propertesting
Subject under tutorship or curatorship
Subject deprived of liberty by a judicial or administrative decision
For healthy volunteers only:
- History of developmental coordination disorder in close relatives (parents,children, siblings).
Study Design
Connect with a study center
Equipe IMPACT du CRNL INSERM U1028, CNRS UMR 5292
Bron, Rhone Alpes 69676
FranceActive - Recruiting
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