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Dispersed Clinical Validation of the Hyfe Cough Monitoring System

NCT06775301 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 31

Last updated 2025-09-05

No results posted yet for this study

Summary

This study will test the accuracy of the Hyfe Cough Monitoring System. This system uses a smartwatch to record the number and pattern of coughs (like a "Fitbit for cough").

The investigators will compare the coughs counted by the Hyfe device with manual cough counts from environmental sounds recordings in the same period.

This is a dispersed observational study and will include individuals with a variety of cough related conditions including but not limited to refractory or unexplained cough, Bronchiectasis, COPD, COVID-19, non-tuberculous mycobacterial infection, tuberculosis, or upper respiratory tract infection.

Conditions

  • Cough Frequency

Interventions

DIAGNOSTIC_TEST

Hyfe Cough Monitoring System

Smartwatch-based cough monitoring

Sponsors & Collaborators

Principal Investigators

  • Peter M Small, MD · Hyfe Inc

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-02
Primary Completion
2025-07-08
Completion
2025-08-29
FDA Device
Yes

Countries

  • Canada

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06775301 on ClinicalTrials.gov