Validation Study With a Non-CE Marked Medical Device (MD)

NACompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

March 2, 2023

Primary Completion Date

November 22, 2024

Study Completion Date

November 22, 2024

Conditions
Chronic Cough
Interventions
DEVICE

SIVA-MVP

Participants receive a small, wearable data recorder, wear it during the day and charge it on the nightstand during sleep for 14x24 hours. The encrypted, recorded segments are uploaded to a server. The server provides a secure environment where the segments are decrypted after receiving the required keys from the patient's SIVA smartphone application. The decrypted segments are then classified as cough by a machine learning algorithm. Participants respond to questions on a smartphone once a day for additional context data. The audio data from the first 24 hours after the patient started wearing the device are used for the validation of the performance of the cough detection algorithm.

Trial Locations (1)

98225

Bellingham Asthma, Allergy & Immunology Clinic, Bellingham

All Listed Sponsors
lead

Siva Health AG

INDUSTRY