Recruiting

Observational Study

Sponsor:

University of Pennsylvania

Code:

NCT06930417

Conditions

Williams Beuren Syndrome

Williams Syndrome

Williams Beuren Region Duplication

Dup7

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Accepted

Study Details

Brief summary:

The goal of this observational natural history study is to better characterize development, transition to adulthood, health and behavior of individuals diagnosed with Williams syndrome (WS) or carrying other variants of 7q11.23 chromosome and to build a DNA and tissue biobank with samples donated by affected individuals. The study has multiple arms focused on different aspects of WS. Participants with genetic diagnosis of WS or other variants of 7q11.23 and their family members are eligible to participate. Study participants may participate in one or multiple arms of the study:

1. Natural History Genotype-Phenotype Study to test the hypothesis that health, behavior, and developmental variability observed in WS is determined by genetic factors and to characterize those genetic changes. Participants of all ages are eligible to participate. Either a blood or saliva sample is required for participation.
2. Biobank: the research team is building a biobank enabling the development of new laboratory tools and models to study WS and test new treatment approaches. A blood sample is required for participation. Participants of all ages are eligible to participate.
3. Development arm of the study aims to delineate the development of language, cognition, personality, literacy and mathematics skills, and adaptive behavior from very early childhood through adulthood in individuals who have WS or Dup7. The purpose of this study also includes determining the predictors of specific aspects of development (e.g., word reading ability, language ability, spatial ability) for individuals with WS or Dup7. Affected individuals of all ages are eligible to participate.
4. Transition to Adulthood study aims to understand how young adults with WS make a successful transition out of high school into adulthood and to help them in this journey by providing a comprehensive psychosocial transition coupled with a medical transition plan. Individuals ages 14-25 years old are eligible to participate. Study requires three in person visits.
5. Health Outcomes, Resilience, Independence, and Executive functioning in Neurodevelopment (HORIZON) aims to characterize physical, mental health, cognitive, social, adaptive, aging, and quality of life outcomes for adults with WS, stress and resilience for caregivers, and the interplay between caregiver stress and resilience with outcomes for adults with WS.
6. Sleep and Activity Study aims to expand knowledge on sleep difficulties experienced by individuals with WS and to better understand the connection between sleep, activity (movement through the day), prescribed medications and other traits in WS.

Conditions

Williams Beuren Syndrome

Williams Syndrome

Williams Beuren Region Duplication

Dup7

Study ID

NCT06930417

Start date

Oct 21, 2024

Status verified date

Jun, 2026

Completion date

Oct 21, 2045

Anticipated

Primary completion date

Oct 21, 2040

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • clinical and/or molecular diagnosis of Williams syndrome (WS)
  • biological parents or siblings of individuals diagnosed with WS
  • molecular diagnosis of 7q11.23 duplication syndrome (Dup7)
  • molecular diagnosis of another abnormality in the 7q11.23 region

Exclusion Criteria:

\- No diagnosis of abnormalities in the 7q11.23 region, while not being a biological relative of affected individuals

Study Design

Enrollment

2000 participants

Anticipated

Interventions and Outcome Measures

Primary outcome measure

  • Assessment of medical concerns in individuals with Williams syndrome and other 7q11.23 variants through review of clinical records. [ Time Frame: Through study completion, an average of 5 years ]
  • Collection and storage of biological specimens (including saliva, blood, and residual tissues) from individuals with Williams syndrome and other 7q11.23 variants to support future translational and genomic research [ Time Frame: Through study completion, an average of 5 years ]
  • Assessment of quality of life of adolescents and adults with WS [ Time Frame: Through study completion, an average of 5 years ]
  • Characterization of behavioral concerns in individuals with Williams syndrome and other 7q11.23 variants through review of medical records. [ Time Frame: Through study completion, an average of 5 years ]
  • Characterizing a caregiver stress for the families affected with Williams syndrome [ Time Frame: Through study completion, an average of 5 years ]

Central Contacts and Locations

Central contacts

Armellino Center of Excellence for Williams syndrome

aceforws@pennmedicine.upenn.edu

Locations

University of Pennsylvania

Recruiting

Philadelphia, Pennsylvania, United States, 19104

Contacts

Armellino Center of Excellence for Williams syndrome

aceforws@pennmedicine.upenn.edu

Principal Investigator:

Carolyn Mervis, PhD

More Information

Sponsor

University of Pennsylvania

Last update posted

Jun 8, 2026

Last verified

Jun, 2026

Keywords

  • williams syndrome
  • Dup7
  • svas
  • 7q11.23
  • autism

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by University of Pennsylvania on 2026-06-08.