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Validating Innovative Biosensors for Rett Autonomic Symptom Tracking

Study acronym: VIBRANT
StatusActive, Not Recruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later Jun 2026 → Nov 2026
See other at-risk trials from Rett Syndrome Research Trust

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Enrollment closed, study ongoing
    • Primary and study completion pushed from Jun 2026 to Nov 2026
    • Study sites: 3 to 2
    v8
  2. Minor Primary and study completion dates: Dec 2025 to Jun 2026
    • Site contacts updated at 1 of 3 sites
    v7
  3. Notable Primary endpoints: 10 to 8
    • Site contacts updated at 1 of 3 sites
    • Study description shortened, about 5 words
    v6
  4. Minor Site contacts updated at 1 of 3 sitesv5
  5. Minor Site details revised at 1 of 3 sitesv4
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  1. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Dec 2025 to Mar 3, 2025
    • Study sites revised (3)
    v3
  2. Notable Primary and study completion dates: May 2025 to Dec 2025
    • Start date: May 2024 to Dec 2025
    • Study title shortened, about 1 word
    v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The VIBRANT study aims to validate biosensors to objectively and directly measure symptoms in Rett syndrome and create confidence in the use of these devices in clinical trials. VIBRANT will use several FDA-cleared wearable biosensors and a non-wearable device to collect symptom data from patients with Rett syndrome for up to 9 weeks. Symptoms of interest include heart rate, breathing, sleep, blood oxygen levels, and movement. Participants will use the biosensors intermittently at home, document device use and symptom status, and will come to the clinic for 1 overnight sleep study. A cohort of up to 10 participants receiving an intervention in a separate clinical trial may also enroll and participate on a custom device schedule for up to 1 year. The study will provide information on the feasibility and ease of use for families at home, biosensor data will be compared to data collected at the same time from the overnight sleep study to demonstrate how well they work in individuals with Rett syndrome, and Emerald will be developed to include movement as a measurable symptom.
Trial Details
NCT Number NCT06338267
Lead Sponsor Rett Syndrome Research Trust
Conditions
(from sponsor)
Rett Syndrome
Related terms Rett Syndrome
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov