Understanding Sleep Problems in Smith-Magenis Syndrome
This study is creating a database to better understand sleep problems in people with Smith-Magenis Syndrome (SMS). It involves collecting information about SMS and sleep disturbances through a web or phone survey. You can participate if you are a parent or legal guardian of an individual with SMS, aged 3 to 65 years. The study aims to track the number of individuals with SMS in the database over five years, which will help create awareness about SMS and its characteristic sleep issues. The current recruitment status is unclear.
- Study design
- This is an observational study aiming to enroll 1000 participants. It involves collecting data through surveys.
- What's involved
- You would provide data related to Smith-Magenis Syndrome and sleep disturbances through a web or phone survey.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary endpoint is measured at 5 years, indicating a long-term data collection period.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Development of Clinical Database of Individuals With Smith-Magenis Syndrome and Sleep Disturbances
At a glance
Conditions
NCT03154697
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Vanda Pharmaceuticals
Washington D.C., District of Columbiastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
Exclusion
What this trial measures
- Number of individuals with Smith- Magenis syndrome5 years