Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04373226
Other study ID # 2020-A00102-37
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 16, 2020
Est. completion date October 20, 2023

Study information

Verified date January 2022
Source Hôpital le Vinatier
Contact Caroline DEMILY, MD PH
Phone 0450915163
Email caroline.demily@ch-le-vinatier.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study ARITH22 will investigate the role of visuo-spatial attention on arithmetic abilities of children with 22q11.2 deletion syndrome.


Description:

Children with 22q11.2 deletion syndrome often have arithmetic learning disability because of magnitude representation impairment. Previous works suggested that magnitude representation impairment could be a result of endogenous visuo-spatial attention dysfunction in 22q11.2DS. Nevertheless this relationship is still poor explored. The influence of visuo-spatial abilities on arithmetic achievement could also be modulated by developmental age. The study ARITH22 will test these hypotheses thanks to magnitude comparisons tasks, in children with 22q11.2 deletion syndrome and matched children without developmental disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date October 20, 2023
Est. primary completion date July 20, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 11 Years
Eligibility Inclusion Criteria: - Diagnosis of 22q11.2 deletion syndrome or no developmental disease - Aged from 4 to 11 years old - French language Exclusion Criteria: - Diagnosis of intellectual deficiency according to DSM 5 criteria - Drug prescribed for somatic condition that could influence cerebral functioning

Study Design


Intervention

Behavioral:
Magnitude comparison tasks and neuropsychological testing
neuropsychological testing (ZAREKI-R) and magnitude comparison tasks with stimuli of different types (visual, visuo-spatial)

Locations

Country Name City State
France Hopital Vinatier Lyon Rhone Alpes

Sponsors (1)

Lead Sponsor Collaborator
Hôpital le Vinatier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of impaired scaled score percentage of impaired scaled score at ZAREKI-R single day
Secondary Percentage of correct responses percentage of correct responses in magnitude comparisons tasks single day
Secondary Mean reaction time mean reaction time in magnitude comparison tasks single day
See also
  Status Clinical Trial Phase
Terminated NCT04639960 - Neuroprotective Effects of Risperdal on Brain and Cognition in 22q11 Deletion Syndrome N/A
Completed NCT01781923 - Cognitive Remediation in 22q11DS N/A
Terminated NCT03284060 - Social Cognition Training and Cognitive Remediation N/A
Completed NCT02895906 - Safety and Efficacy Study of NFC-1 in Subjects Aged 12-17 Years With 22q11.2DS & Associated Neuropsychiatric Conditions Phase 1
Recruiting NCT04639388 - Understanding of Psychotic Disorders in Children With 22q11.2DS N/A
Completed NCT00916955 - Genetic Modifiers for 22q11.2 Syndrome
Recruiting NCT05924347 - Early Scoliotic Changes in Children at Increased Risk for Scoliosis Development
Recruiting NCT00556530 - Examining Genetic Factors That Affect the Severity of 22q11.2 Deletion Syndrome
Completed NCT02460328 - Resolution of Primary Immune Defect in 22q11.2 Deletion Syndrome N/A
Completed NCT04647500 - Effects of Methylphenidate on Brain and Cognition in 22q11 Deletion Syndrome N/A