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This is a minimal risk case-controlled single arm intervention study, including 10 patients with a prior history of takotsubo and 10-age and sex matched healthy controls. Subjects will undergo in laboratory testing to measure autonomic function. They will then undergo a 15-week program of device-guided breathing with remote measures of autonomic function obtained at home. Analysis will determine the reproducibility of home autonomic measures and the provide preliminary data to determine the efficacy of device-guided breathing on autonomic measures and quality of life in patients with takotsubo.
Age
21 - No limit years
Sex
ALL
Healthy Volunteers
No
New York University School of Medicine
New York, New York, United States
Start Date
October 1, 2021
Primary Completion Date
June 1, 2027
Completion Date
June 1, 2027
Last Updated
March 5, 2026
24
ESTIMATED participants
Tako Breath
DEVICE
Lead Sponsor
NYU Langone Health
Data Source & Attribution
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