Actively Recruiting
The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome, Williams Syndrome, and Fragile X Syndrome: Characterization, Treatment, and Connection to Developmental and Molecular Factors
Led by The Chaim Sheba Medical Center · Updated on 2026-03-18
400
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research investigates the psychiatric and cognitive characteristics in people with Velocardiofacial Syndrome (VCFS), Williams Syndrome (WS), and Fragile X Syndrome. It also explores connections between these conditions and developmental or molecular factors. The study is a phase 4 clinical trial aimed at better understanding these complex syndromes and their treatment responses. Participants will undergo evaluations that include cognitive testing both without and with the drug methylphenidate. The study also involves the use of other medications such as fluoxetine and risperidone to assess their effects. These treatments are being studied to observe their impact on psychiatric and cognitive symptoms in the syndromes mentioned. During the study, participants will have psychological assessments and molecular tests over a two-year period. Researchers will measure responsiveness to medical treatments and track changes in cognitive and psychiatric phenotypes. The study is non-blinded and sponsored by The Chaim Sheba Medical Center. Participants can expect monitoring and follow-up assessments to understand treatment effects and underlying biological factors.
CONDITIONS
Brief Title
The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Chromosomal deletion proven by FISH examination
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 2 years
Participants undergo cognitive and psychological evaluations, including assessments before and after administration of medications such as methylphenidate.
Multiple assessments over 2 years
Trial Site Locations
Total: 1 location
1
Schneider Children's Mediac Center of Israel
Petah Tikva, Israel, 49202
Actively Recruiting
Research Team
D
Doron Gothelf, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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