ClinicalTrials.gov. Wearable Technology in the Detection and Evaluation of Sleep-Related Breathing Disorders (ReSTech)

Publicamos el protocolo del proyecto ReSTech (SleepWear) en ClinicalTrails. El proyecto que estamos desarorllando en colaboración con el servicio de Neumología del Hospital Álvaro Cunqueiro de Vigo está ya disponible para su consulta y seguimiento a través de la plataforma ClinicalTrials. Este proyecto ha recibido ya el aprovado del Comité de ética de Investigación Clínica de Galicia el pasado 23 de julio de 2024. El objetivo es validar la calidad de medición de las pulseras deportivas de uso domñestico mcomo primer indicador de patologias de sueño.

ClinicalTrials.gov ID NCT06606691

Wearable Technology in the Detection and Evaluation of Sleep-Related Breathing Disorders (ReSTech)

Study Overview

This project is an observational study that aims to evaluate the accuracy of wearable devices in detecting potential sleep-related breathing disorders (SRBD) in individuals visiting the Sleep-Related Breathing Disorders and Home Ventilation Unit. The main goal of the study is to determine if wearable devices, like sleep and activity-tracking wristbands and watches, can effectively supplement the detection of these disorders.

The study will analyze various variables related to sleep quality and quantity. Participants will be asked to wear a Xiaomi Mi Band 8 device during an overnight hospital polygraphy test, which will be conducted for one day in their usual daily environment. Additionally, at the beginning of their participation, they will need to complete a questionnaire collecting information about sociodemographic variables, daily habits, routines, and their assessment using the Epworth Sleepiness Scale.

After completing the polygraphy test and using the Xiaomi device, participants will be required to answer another questionnaire addressing aspects related to their sleep quality and habits during this period.