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Digital Acoustic Surveillance for Early Detection of Respiratory Disease Outbreaks

Digital Acoustic Surveillance for Early Detection of Respiratory Disease Outbreaks: An Exploratory Observational Study in Navarra, Spain

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04762693
Enrollment
930
Registered
2021-02-21
Start date
2020-11-11
Completion date
2022-05-24
Last updated
2022-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cough, Covid19

Keywords

chronic cough, Covid19, Acoustic surveillance

Brief summary

An observational study to evaluate the accuracy of a digital cough monitoring tool to reflect the incidence of COVID-19 and other respiratory infections at the community level in the city of Pamplona, Spain.

Detailed description

This is a single-center prospective observational study that pretends to evaluate the accuracy of an acoustic surveillance mobile app to detect individual episodes of cough among a monitored population, as well as the barriers and facilitators that might affect uptake of similar platforms at a population level. The app in question, Hyfe cough tracker, runs in the background of smartphones, and records short snippets (\<0.5 seconds) of explosive, putative cough sounds. These are then classified as cough or non-cough, using a convolutional neural network (CNN) model, and matched to GPS and time data collected by the smartphone. The night-time cough of participants will be monitored for a 30-day period, and their clinical records will be reviewed regularly, specifically looking for diagnoses of cough-producing diseases, and with special emphasis on COVID-19. Cough data will be used to create a heatmap of cough density and geographic distribution. Aggregated cough registries will be used to calculate the coughs per person-hour registered in the cohort. These data will be used to carry out an ARIMA analysis on three parallel time series at the community level: The incidence of respiratory disease in the monitored cohort, in the entire study area (including the Universidad de Navarra, and the neighbouring Cendea de Cizur), and the cough frequency per monitored hours. Changes in cough frequency will also be compared to other environmental variables such as temperature and pollution level registered in the study area.

Interventions

A mobile app that runs in the background of smartphones and detects putative cough sounds.

Sponsors

Centre de Recherche du Centre Hospitalier de l'Université de Montréal
CollaboratorOTHER
Clinica Universidad de Navarra, Universidad de Navarra
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
13 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* Be aged 13 or above, * Own and regularly use a smartphone able to run the cough-tracking system, * Be willing to install and regularly use it, * Be current residents of Navarra, and * Have an active relationship with the university (having interest in the study, or being a student or worker, be a patient with a cough-related diagnosis at the Clínica Universidad de Navarra, or Cizur's health centre).

Exclusion criteria

* Inability to accept the privacy policy and terms of use of the cough-tracking system. * Inability to grant access to medical records.

Design outcomes

Primary

MeasureTime frameDescription
Correlation between registered coughs per person-hour and incidence of respiratory diseases1 yearThe investigators will run an ARIMA analysis with three parallel time series: aggregated incidence of respiratory diseases in the observed cohort, in the entire study area, and aggregated cough data.

Secondary

MeasureTime frameDescription
Uptake of the surveillance system1 yearThe investigators will calculate the proportion of the total reached, eligible population that installs the app and regularly uses it in the requested way.
Barriers and facilitators affecting uptake of the surveillance system1 monthA sub-sample of 25 participants will be randomly recruited for focus group discussions. In the focus groups, researchers will ask participants the following general questions: (1) What do you like about the app, (2) what do you think of this app relative to other health apps, (3) what doesn't work well, (4) what keeps you committed (or not) to using the app, (5) what do you think the purpose of the app is, (6) do you think the app has commercial value, and (7) what advice do you have for the developers?

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026