Brace Monitoring for Adolescent Idiopathic Scoliosis (AIS)

Recruiting N/A Interventional Study
Adolescent Idiopathic Scoliosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
8 – 17
Sex
Female
Study type
Interventional
Purpose
Device Feasibility
Participants needed
87 (estimated)
Sponsor
Columbia University · Other
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About This Trial
The overall aim of the study is to utilize a novel device and smartphone application in order to improve measurement of patient compliance with at-home bracing for scoliosis as well as create a more accurate assessment of brace fit via continuous and objective measures of tension. These ground-breaking metrics will provide analyzable data to more accurately reflect and predict actual patient compl…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Diagnosis of Adolescent Idiopathic Scoliosis (AIS) * Sanders skeletal stage 4 or earlier * Clinician-recommended Rigo bracing * Patient receiving brace treatment Exclusion Criteria: \- Prior spine surgery
Contacts

Benjamin D. Roye, MD, MPH

(212) 305-5475

bdr5@columbia.edu

CONTACT