Ring-type Pulse Oximeter for Evaluation for Sleep Assessment Study

NCT ID: NCT06221124

Last Updated: 2024-01-24

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-07-15

Study Completion Date

2023-06-12

Brief Summary

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Recently, various electronic lifestyle activity monitoring devices (ELAM) are increasingly commercially available. However, the quality and reliability of the data from ELAM are unclear, compared with polysomnography (PSG), which is the gold-standard sleep assessment method. Thus, combining ELAM with PSG will validate ELAM and improve its clinical and research utilization.

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.

Detailed Description

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Conditions

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Sleep-Disordered Breathing Sleep Architecture

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

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.

Group Type EXPERIMENTAL

Belun Ring Pulse Oximeter

Intervention Type DEVICE

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.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Age between 18 to 80 years old. Ideally balanced for sex and age (18 to 80 years old)
* 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

* Presence of any significant systemic or unstable medical condition which could lead to difficulty complying with the protocol, suicidality, current regular use of psychiatric medications, opiates, or thyroid medications, dementia, current substance abuse, post-traumatic or psychotic disorders, bipolar disorder; any significant neurologic disease, including possible and probable dementia, Parkinson's or Huntington's disease, brain tumor, progressive supranuclear palsy, seizure disorder, subdural hematoma, multiple sclerosis, history of significant head trauma, history of alcohol or substance use disorder within the past 2 years (DSM V criteria);
* If positive airway pressure (PAP) titration study or split night study (diagnostic and PAP titration study combined)
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stanford University

OTHER

Sponsor Role collaborator

Belun Technology Company Limited

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Stanford Sleep Medecine Center

Redwood City, California, United States

Site Status

Countries

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United States

Other Identifiers

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SPO#179613

Identifier Type: -

Identifier Source: org_study_id

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