Rett Syndrome Clinical Trials

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Auditory EEG and Behavioral Assessments in Individuals With Rett Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

This observational research study is designed to learn more about how the brain processes sound in individuals with Rett syndrome. Participants will complete a noninvasive electroencephalogram (EEG) recording while listening to simple sounds through headphones. In addition, parents or caregivers will complete questionnaires and an interview about the participant's symptoms, communication abilities, daily functioning and overall health. The information collected from this study may help researchers better understand brain activity patterns and clinical features associated with Rett syndrome and support future research efforts.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Healthy Volunteers: t
View:

• Have a clinical diagnosis of classic Rett syndrome

• Have a pathogenic MECP2 genetic variant confirmed via genetic testing

• Are past the clinical regression stage

• Are within the eligible age range for the study (2 years or older)

• Are able to tolerate the noninvasive EEG recording

• Parent or caregiver is willing and able to provide parental permission and complete questionnaires and interviews

• Neurologically healthy individuals ages 2 years or older

• Are able to tolerate the noninvasive EEG recording

Locations
United States
New York
Center for Advanced Brain Imaging and Neurophysiology, University of Rochester Medical Center
RECRUITING
Rochester
Time Frame
Start Date: 2025-07-31
Estimated Completion Date: 2027-08
Participants
Target number of participants: 60
Treatments
Rett Syndrome Participants
Individuals with Rett syndrome who participate in this observational study will undergo a noninvasive electroencephalogram (EEG) recording while listening to simple sounds through headphones. Parents or caregivers will complete questionnaires and interviews related to the participant's symptoms, communication abilities, daily functioning and overall health. A Rett syndrome severity scale may also be completed by a clinician or trained member of the research team.
Age- and sex-matched controls
Individuals who are age- and sex-matched to Rett syndrome participants in this study will be enrolled as controls. Control participants must have no medical history of genetic, neurological, or psychiatric disorders, no history of special education services, and no hearing impairment. Control participants in this study will undergo a noninvasive electroencephalogram (EEG) recording while listening to simple sounds through headphones. Control participants (or their parent) will also complete a demographics questionnaire.
Related Therapeutic Areas
Sponsors
Leads: University of Rochester

This content was sourced from clinicaltrials.gov