Actively Recruiting

Phase 4
All Genders
ID00768820

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

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Chromosomal deletion proven by FISH examination
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

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

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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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