Chromosome 22q11.2 deletion syndrome (22q11DS) is a neurogenetic condition associated with a high risk of psychiatric disorders, including schizophrenia spectrum disorders. This population is characterized by a specific neurocognitive profile and atypical brain development. Methylphenidate is a psychostimulant used in the treatment of attention deficit with/without hyperactivity (ADHD). Although ADHD is one of the most important co-morbidities in 22q11DS, affecting 35-45% of patients, to date only two studies have focused on quantifying the efficacy of this treatment in this population. The objective of this study is to quantify the improvement in cognitive performance as well as the differences in brain connectivity associated with the methylphenidate molecule in a population at risk of cognitive impairment and the development of schizophrenia.
Age range
8 Years – 25 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Conners' Continuous performance test, third edition (CPT-3)
Timeframe: CPT-3 pre-treatment
Conners' Continuous performance test, third edition (CPT-3)
Timeframe: CPT-3 6 days of treatment
Conners' Continuous performance test, third edition (CPT-3)
Timeframe: CPT-3 one month after the end of treatment
Stroop task
Timeframe: Stroop inhibition ratio pre-treatment
Stroop task
Timeframe: Stroop inhibition ratio 6 days of treatment
Stroop task
Timeframe: Stroop inhibition ratio one month after the end of treatment
Letter-number sequencing
Timeframe: Letter-number Sequencing pre-treatment
Letter-number sequencing
Timeframe: Letter-number Sequencing 6 days of treatment
Letter-number sequencing
Timeframe: Letter-number Sequencing one month after the end of treatment
Color Trails test (CTT)
Timeframe: CTT flexibility ratio pre-treatment
Color Trails test (CTT)
Timeframe: CTT flexibility ratio 6 days of treatment
Color Trails test (CTT)
Timeframe: CTT flexibility ratio one month after the end of treatment
Cambridge Neuropsychological Test Automated Battery (CANTAB)
Timeframe: CANTAB pre-treatment
Cambridge Neuropsychological Test Automated Battery (CANTAB)
Timeframe: CANTAB 6 days of treatment
Cambridge Neuropsychological Test Automated Battery (CANTAB)
Timeframe: CANTAB one month after the end of treatment
15 signes & 15 words
Timeframe: 15 signes & 15 words pre-treatment
15 signes & 15 words
Timeframe: 15 signes & 15 words 6 days of treatment
15 signes & 15 words
Timeframe: 15 signes & 15 words one month after the end of treatment
ADHD symptoms
Timeframe: ADHD symptoms pre-treatment
ADHD symptoms
Timeframe: ADHD symptoms 13 days of treatment
ADHD symptoms
Timeframe: ADHD symptoms one month after the end of treatment