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Technical Feasibility Study on Screening Sleep Related Breathing Disturbances and Sleep Apnoea With Wearable Sensors

NCT05235984 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2023-10-11

No results posted yet for this study

Summary

In this study the feasibility of detecting sleep apnoeas with unobtrusive wearable sensors and sounds recorded with a smartphone is studied by making an overnight recording to patients with high probability of sleep apnoeas. The data acquired with the aforementioned devices is: ECG, acceleration, bioimpedance of thorax and processed and raw audio. In data analysis phase it will be studied which combinations of these signals would enable detecting sleep apnoeas with high enough sensitivity and specificity when compared to a night polygraphy reference (Nox T3 device using airflow, breathing movements, audio, position, movement, oxygen saturation, pulse and leg EMG).

Conditions

Sponsors & Collaborators

  • CSEM Centre Suisse d'Electronique et de Microtechnique SA - Recherche et Developpement

    collaborator INDUSTRY

  • Firstbeat Technologies Oy

    lead INDUSTRY

Principal Investigators

  • Juha K Heiskala, LM, DSc · Neurophysiologist at HUS (Hospital district of Helsinki and Uusimaa) and at KNF-Laboratoriot Oy

  • Ilkka Korhonen, DSc · CTO at Firstbeat Technologies and Associate Professor at Tampere University

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-18
Primary Completion
2023-09-30
Completion
2023-09-30

Countries

  • Finland

Study Locations

More Related Trials

Entities

Diseases

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 NCT05235984 on ClinicalTrials.gov