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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02899676
Other study ID # 2013.801
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 18, 2014
Est. completion date May 9, 2018

Study information

Verified date March 2019
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study was to identify neural correlates involved in arthmetics processing in adults and children aged 8 to 14 with normal cognitive function. Brain area will be identified by functional magnetic resonance imaging (IRMf).


Recruitment information / eligibility

Status Completed
Enrollment 79
Est. completion date May 9, 2018
Est. primary completion date May 9, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years to 24 Years
Eligibility Inclusion Criteria:

- children aged 8 to 14 with parents' consent

- adults aged 18 to 24

- right-handed

- affiliated to the French social security

Exclusion Criteria:

- known neurological disorders including epilepsia

- known psychiatric disorders including Attention Deficit Disorder

- birth complications needing intensive care

- central nervous system treatment

- important hearing disabilities

- not corrected impaired vision

Study Design


Related Conditions & MeSH terms

  • Neural Bases of Arithmetic Processing

Intervention

Other:
neuropsychological testing

functional magnetic resonance imaging

simple arithmetic operations


Locations

Country Name City State
France Médecine nucléaire, Groupement Hospitalier Est, HCL Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Brain area activity in arithmetic processing will be identified by IRMf Brain activity is identified by IRMf up to 60 days after inclusion
Secondary Parietal region activity in arithmetic processing will be identified by IRMf comparison between group aged to 12to 14 and group aged to 8 to 11 up to 60 days after inclusion