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NOT YET RECRUITING
NCT02998502
NA
The Use of a FDA Cleared, Drug-free, Breathing System for Anxiety and Panic Disorders in Children and Teens
Sponsor: Johns Hopkins University
View on ClinicalTrials.gov
Summary
This study will test the efficiency of the Freespira Breathing System in youth.
Official title: Efficacy of a Biofeedback Breathing System for Anxiety and Panic Disorders
Key Details
Gender
All
Age Range
9 Years - 17 Years
Study Type
INTERVENTIONAL
Enrollment
73
Start Date
2026-08-01
Completion Date
2027-03-01
Last Updated
2026-03-09
Healthy Volunteers
No
Conditions
Interventions
DEVICE
Freespira Breathing System
Over an 8-week period the efficacy of the FBS system in youth will be tested, with those in the randomized active device group. The control group will not receive the device until completion of the 8 week baseline.
Locations (1)
Johns Hopkins University
Baltimore, Maryland, United States