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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

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