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Study identifier: NCT07655492 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Developing a Tailored Neuropsychological Rehabilitation for Sturge-Weber Syndrome

Condition: Sturge - Weber Syndrome (SWS)  ·  Sponsor: University of Roma La Sapienza

PhaseN/A
Planned participants40
Who can joinAll sexes, 2 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this observational study is to learn about the neuropsychological profile of Sturge-Weber Syndrome (SWS) in children and adults with this rare neurocutaneous condition. SWS affects approximately 1 in 50,000 live births and is characterized by brain blood vessel malformations, facial port-wine stains, and abnormal vascularization in the brain, skin, and eyes. Patients are at high risk for epileptic seizures, stroke-like episodes, glaucoma, and motor and cognitive difficulties. The main questions it aims to answer are: * What are the specific cognitive strengths and weaknesses in visuospatial abilities, working memory, and executive functions in individuals with SWS? * What is the detailed neuropsychological profile of patients with SWS who do not have intellectual disability? * Are there different cognitive-behavioral phenotypes between patients with and without the characteristic facial port-wine stain (PWS)? * How do clinical variables such as seizure history and brain involvement patterns relate to specific cognitive deficits? Participants will undergo a comprehensive neuropsychological assessment battery that includes: * Intellectual functioning tests (K-BIT2) to measure verbal and non-verbal intelligence * Executive function evaluation (BRIEF2) assessing behavioral regulation, emotional regulation, and cognitive regulation * Language assessment including receptive vocabulary (PPVT) and grammatical comprehension (TCGB-2) * Visuospatial skills testing (Beery-…

This description comes directly from the study's public registry record.

Talk to the study team

Laura Piccardi, PhD  ·  +39 06 49917527  ·  laura.piccardi@uniroma1.it

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Psychology University of RomeRoma, Roma, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT07655492