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临床试验/NCT06474351
NCT06474351已完成不适用

Development and Fine-tuning of a Medical-grade Wearable Device with Interpretable Artificial Intelligence System for the Obstructive Sleep Apnea-hypopnea Syndrome (OSAHS) Screening

PranaQ Pte. Ltd.1 个研究点 分布在 1 个国家目标入组 240 人开始时间: 2023年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
240
试验地点
1
主要终点
Apnea Hypopnea Index(AHI)

研究概览

简要总结

The clinical study aims to develop and fine-tune the TipTraQ system, created by PranaQ, for home sleep apnea screening. The system comprises a wearable device and a cloud-based AI for estimating Total Sleep Time (TST) and Apnea-Hypopnea Index (AHI). This open-label, non-randomized study will recruit 240 subjects aged 20 and older from the Veteran General Hospital, Taipei.

详细描述

Sleep Breathing Disorders (SBD) is a common disorder in the population. However, a lot of patients are not aware of this disease and do not receive proper treatment, which not only impacts their personal health but also causes public disasters. Thus, a screening tool to find those patients becomes a critical point-of-care issue. To achieve this goal, a wearable device that is suitable for the screening is needed. The goal of this study is developing and fine-tuning a new sleep screening platform, TipTraQ, developed by PranaQ. TipTraQ is composed of a wearable device designed as a convenient screening device based on the photoplethysmography (PPG) technique and an interpretable artificial intelligent (AI) system that takes the PPG signal recorded by the wearable device as input and outputs and outputs estimated total sleep time (TST) and apnea-hypopnea index (AHI).

The study is open-label and non-randomized, planning to recruit 240 subjects. Participants will use the TipTraQ device alongside a companion mobile app, with data analysis supported by AI technology hosted on a cloud server. The TipTraQ device will be worn over fingertip. The primary goal is to assess the robustness of the TipTraQ system and fine-tuned the algorithm by comparing its output against the gold standard PSG annotations made by sleep experts.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects from the age of 20 and older that have an indication for an in-lab PSG study. The subject should be able to understand the study and sign the informed consent before being enrolled in the study. During the study period, the subject can withdraw from the study any time.

排除标准

  • Subjects with the following medical conditions will be excluded from this study:
  • Heart transplant
  • Heart failure, New Youk Heart Association (NYHA) classification III or IV
  • Chronic opioid medication user Devastating Severe strokes, with the modified Rankin score (mRS)≥4
  • Tracheostomy
  • Incapable of comprehending and signing the informed consent and questionnaires, including but not limited to subjects with severe Alzheimer's, unconscious by head trauma, or of someone with limited mental capacity
  • Cannot correctly follow the order to use the TipTraQ device

结局指标

主要结局

Apnea Hypopnea Index(AHI)

时间窗: From the start of a single polysomnography study to the end of the recording. Usually range from 4 to 10 hours

the combined average number of apneas and hypopneas that occur per hour of sleep

Total Sleep Time(TST)

时间窗: From the start of a single polysomnography study to the end of the recording. Usually range from 4 to 10 hours

Total sleep time during the polysomnography (PSG)

Oxygen Desaturation Index(ODI)

时间窗: From the start of a single polysomnography study to the end of the recording. Usually range from 4 to 10 hours

Average desaturation episodes with a decrease in the oxygen saturation of ≥4% or 3% per hour

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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