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Validation of the C-mo System - Cough Monitoring
Sponsor: Cough Monitoring Medical Solutions
Summary
The goal of this clinical study is to validate C-mo System's ability to automatically detect and characterise cough, in patients over 2 years old with cough as a key or refractory symptom. The main questions it aims to answer are: 1. Can C-mo System detect cough events? (automatic cough detection) 2. Can C-mo System characterise cough events? (calculation of cough intensity, identification of cough type and presence of wheeze in detected coughs) Participants will be asked to: * Wear the C-mo Wearable device for 24 hours (1 day); * Complete a diary with relevant activities throughout the monitoring period; * Fill-out questionnaires related to coughing frequency and intensity, usability of the device, and impact of cough on quality of life.
Key Details
Gender
All
Age Range
2 Years - Any
Study Type
INTERVENTIONAL
Enrollment
300
Start Date
2023-12-11
Completion Date
2026-09
Last Updated
2026-04-08
Healthy Volunteers
No
Conditions
Interventions
C-mo System
Patients will use C-mo System for a period of 24h, to assess cough characteristics.
Locations (8)
HPAV - Trofa Saúde Hospital de Alfena
Alfena, Portugal
HFF - Hospital Professor Doutor Fernando Fonseca
Amadora, Portugal
Lab3R - Laboratório de Investigação e Reabilitação Respiratória da Escola Superior de Saúde da Universidade de Aveiro
Aveiro, Portugal
CHUC - Centro Hospitalar e Universitário de Coimbra
Coimbra, Portugal
HDE - Hospital Dona Estefânia
Lisbon, Portugal
NMS Research - Laboratório de Exploração Funcional | Fisiopatologia
Lisbon, Portugal
CHUSJ - Centro Hospitalar Universitário de São João
Porto, Portugal
ICUFP - Instituto CUF Porto
Porto, Portugal