Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03128125
Other study ID # MOHPI (RB 16.145)
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 6, 2017
Est. completion date August 22, 2018

Study information

Verified date October 2020
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of this study is to determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children.


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date August 22, 2018
Est. primary completion date August 22, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 16 Years
Eligibility Inclusion Criteria:

All participants :

- Informed consent of the child and both parents obtained

- Affiliated to Social Security

- Participants must be between 6 and 16 years of age.

Child with high intellectual potential :

- Score = 130 on an intellectual efficiency scale administered by a psychologist

Control child :

- They will have to be intellectually efficient in the standard. To ensure this, the two sub-tests of the Intellectual Efficiency Scale (WISC-V) most closely correlated with intelligence (Vocabulary and Matrices) will be administered to them. Thus, the child must meet one of the following criteria in order to be included:

- Have two standard notes between -1 and +1 DS (between 7 and 13);

- Have one of its two notes between -1 and + 1DS (between 7 and 13) and the other between -2DS and <+ 2DS (between 5 and 15).

Exclusion Criteria:

All participants :

- Neurological history (epilepsy, cranial trauma, prematurity ...)

- Psychiatric history (Autistic Spectrum Disorder ...),

- Known genetic disease,

- Motor deficiency (eg hemiplegia),

- Elementary sensory disorder (auditory and visual) or insufficient command of French, limiting the understanding and participation in the study likely to impact the results to the protocol.

- Gnosic visual or linguistic deficiency.

- Sensory disorder

- Psychotropic Intake

Control child :

- High intellectual potential

- Known or suspected learning disability (no dyslexia-dysorthography, dysphasia, dyspraxia, dyscalculia).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
clinical examination in neurology
This examination is based on the movement of the child in a standing position (forward and backward on a straight line, jumping on a foot ...), seated (visual continuation ...) and elongated (tone, patellar and achillian reflexes, superficial sensitivity ...) . This makes it possible to evaluate all the neurological systems.
neuropsychological examination
This examination is based on the use of standardized psychometric tools and validated with children, usually used in clinical practice.
anamnestic elements
Several elements will be collected during the clinical interview to inform the history of the child's development, such as neonatal data (term of pregnancy, APGAR score ...), age of appearance of the first words , seating, walking, possible care, level of education ans level of education of the parents.

Locations

Country Name City State
France University Hospital Brest

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children with WISC-V scale (Wechsler). 1 day
Primary Neurological assessments Dysfunction (yes/no) for children with high intellectual potential compared to control children. 1 day
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children. With Purdue Pegboard test. 1 day
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children. With subtest Fluence Verbale (NEPSY-II) 1 day
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children. With subtest of motricity (NEPSY-II) 1 day
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children. With Rey test 1 day
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children. With writing test (BHK) 1 day
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children. With New card sorting test 1 day
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children. With comportemental scale (BRIEF) 1 day
Primary Neuropsychological assessment Determine whether children with high intellectual potential have gestural and / or executive difficulties compared to control children. With M-ABC-II questionary 1 day
See also
  Status Clinical Trial Phase
Completed NCT03563196 - Diagnosis Of Pulmonary Complications After Cardiac Surgery In Children
Completed NCT02553486 - Internationally Adopted Children Quality of Life N/A
Completed NCT02918890 - Intensive Unimanual (CIMT) and Bimanual Training (HABIT) in Children With Hemiplegia N/A
Completed NCT02903134 - Early Risk of Asthma in Children Exposed to In-utero Maternal Obesity
Active, not recruiting NCT01874847 - PLAY GAME: Post-concussion Syndrome in Youth - Assessing the GABAergic Effects of Melatonin Phase 2/Phase 3
Enrolling by invitation NCT01971827 - Effectiveness of a Physical Activity Intervention to Prevent Obesity and Improve Academic Performance N/A
Enrolling by invitation NCT01971840 - Effectiveness of a Physical Activity Intervention on Preventing Obesity During the Adiposity Rebound Period. N/A
Completed NCT01738308 - The Effects of Healing Touch on Post Operative Pediatric Patients N/A
Completed NCT01864811 - Effect of Baby-CIMT in Infants Younger Than 12 Months N/A
Completed NCT01693926 - Effect of Physical Activity an Stress in Children N/A
Completed NCT01943760 - Tamadol Wound Infiltration in Children Under Inguinal Hernioplasty Phase 4
Completed NCT01323010 - Efficacy and Safety of Increasing Doses of Inhaled Albuterol in Children With Acute Wheezing Episodes N/A
Completed NCT01277224 - Effectiveness of a Physical Activity Intervention on the Obesity of Schoolchildren N/A
Active, not recruiting NCT00989547 - Cord Blood Infusion for Type 1 Diabetes Mellitus (T1DM) Phase 1
Completed NCT04051723 - Pre-emptive Scalp Infiltration With Dexamethasone Plus Ropivacaine for Post-Craniotomy Pain in Children Phase 4
Completed NCT03236337 - Effectiveness of MOVI Interventions on Adiposity, Cognition and Subclinical Atherosclerosis: MOVI-daFit! N/A
Completed NCT03236363 - Effectiveness of MOVI Interventions on Adiposity, Cognition and Motor Competence: MOVI-da10! N/A
Not yet recruiting NCT03427697 - Effect of VR and Accommdation Relax on Controlling Myopia in Children N/A
Completed NCT05603507 - Inspiratory Muscle Training in Children With Chest Burn N/A
Not yet recruiting NCT06267339 - Effects of Transcranial Random Noise Stimulation on Motor Learning in Typically Developing Adolescents Early Phase 1