Psychometric Validation of the Competitive Attention Test
- Conditions
- Attention Deficit Hyperactivity Disorder
- Registration Number
- NCT03942835
- Lead Sponsor
- Hospices Civils de Lyon
- Brief Summary
This project aims at validating a new neuropsychological test to measure voluntary and involuntary attention for clinical use to diagnose attentional deficits.
This project proposes:
* a test-retest procedure in healthy subjects aged from 6 to 90 year-old;
* testing in attention deficit hyperactivity disorder (ADHD) patients before psychostimulant treatment;
* testing in attention deficit hyperactivity disorder (ADHD) patients before psychostimulant treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 26
healthy major participants:
- Age from 18 to 90 year-old
- Informed consent to participate in the study
- No neurological or psychiatric disorder
- No history of neuro-psychiatric disorder or neurodevelopmental type dysphasia, dyslexia, dyspraxia, attention deficit disorder
healthy minor participants:
- Age from 6 to 17 year-old
- Informed consent of parents or guardians for the child's participation in the study
- No neurological or psychiatric disorder
- No history of neuro-psychiatric disorder or neurodevelopmental type dysphasia, dyslexia, dyspraxia, Attention deficit disorder
ADHD minor patients:
- Age from 6 to 17 year-old
- Informed consent of parents or guardians for the child's participation in the study
- ADHD Diagnosis with or without hyperactivity
- No psychiatric history other than ADHD.
- For Experience 3: treatment in progress.
healthy major participants
- Age below 18 or above 90 year-old
- unaffiliated or non-beneficiaries of the social security scheme
healthy minor participants:
- Age below 6 or above 18 year-old
- unaffiliated or non-beneficiaries of the social security scheme
ADHD minor patients:
- Age below 6 or above 18 year-old
- unaffiliated or non-beneficiaries of the social security scheme
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Reaction times in healthy subjects and patients with ADHD. 6 weeks Reaction times in milliseconds obtained with the CAT test in healthy participants and in patients with ADHD.
- Secondary Outcome Measures
Name Time Method Percentage of correct responses in healthy subjects and patients with ADHD. 6 weeks Percentage of correct responses obtained with the CAT test in healthy participants and in patients with ADHD.
Trial Locations
- Locations (1)
Centre de Recherche en Neurosciences de Lyon, INSERM U1028
🇫🇷Bron, France