Ring-type Pulse Oximeter for Evaluation for Sleep Assessment Study
NCT ID: NCT06221124
Last Updated: 2024-01-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2020-07-15
2023-06-12
Brief Summary
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The investigators propose to conduct this study to validate ELAM device for sleep assessment. The investigators will compare Belun Ring data collection and overnight in-lab PSG measures of Sleep-Disordered Breathing (SDB) and sleep architecture in adults with obstructive sleep apnea (OSA) symptoms.
The investigators propose to recruit a total of 40 participants with symptoms of OSA. The overall accuracy, sensitivity and specificity of Belun Ring to assess SDB and sleep architecture will be validated by using PSG analysis as a gold standard.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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BEL-Participant
First, we will measure the size of the finger of the participant and select appropriate size of Belun Ring device and the participant will be instructed to wear it on a finger in addition to regular PSG set up on the night of sleep study. Simultaneous recording of Belun Ring data {pulse oximeter, pulse rate and actigraphy} and standard PSG will be performed for one night.
Belun Ring Pulse Oximeter
Belun Ring Pulse Oximeter allows measurement and analysis of oximetry, pulse rate, photo-plethysmography (PPG), and accelerometer signals from the proximal phalanx of index finger. Sleep stage (bSTAGES) and respiratory event index (bAHI) are estimated.
Interventions
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Belun Ring Pulse Oximeter
Belun Ring Pulse Oximeter allows measurement and analysis of oximetry, pulse rate, photo-plethysmography (PPG), and accelerometer signals from the proximal phalanx of index finger. Sleep stage (bSTAGES) and respiratory event index (bAHI) are estimated.
Eligibility Criteria
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Inclusion Criteria
* no more than 75% of subjects in one bin of: (male, female)
* no more than 50% of subjects in one age-group (18-29, 30-39, 40-49, 50-59, 60-80)
* Patients with OSA symptoms (snoring, excessive daytime sleepiness or witnessed apnea, etc.)
* Without any unstable medical or psychiatric co-morbidities that would be expected to interfere with the study.
* If taking any medication, must be on a stable dose of medication for a month
* Able to read and understand English
Exclusion Criteria
* If positive airway pressure (PAP) titration study or split night study (diagnostic and PAP titration study combined)
18 Years
80 Years
ALL
No
Sponsors
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Stanford University
OTHER
Belun Technology Company Limited
OTHER
Responsible Party
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Locations
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Stanford Sleep Medecine Center
Redwood City, California, United States
Countries
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Other Identifiers
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SPO#179613
Identifier Type: -
Identifier Source: org_study_id
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