- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01680380
Tracking Breathing During Sleep With Non-contact Sensors
Study Overview
Status
Conditions
Detailed Description
Subjects will be asked to place non-contact sensors (for example, ambient microphones, wireless movement sensors) in their home sleep environment. No sensors will be attached to or otherwise in contact with the subject's body. The subjects will start the data collection before they fall asleep, and stop the data collection the next morning when they wake. The subjects will then return the sensors to the investigator for analysis.
The investigators will study the data and associated manual labeling. The investigators will develop algorithms that use statistical and machine-learning methods to train computer models designed to track breathing automatically. The investigators will compare the automatic output against manually generated labels to determine breath-tracking accuracy.
Study Type
Contacts and Locations
Study Locations
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Oregon
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Portland, Oregon, United States, 97239
- Center for Spoken Language Understanding
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age 21-89
- No self-reported sleep breathing problems
Exclusion Criteria:
- Positive diagnosis for sleep breathing problem (e.g., obstructive sleep apnea)
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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At-Home
Overnight sleep at home
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Breathing sounds are evident in overnight audio recordings
Time Frame: Night of recording
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This study aims to track breathing during sleep using a high-quality audio interface.
Our primary objective is to determine if quiet breathing sounds are visible (in the spectral domain) to trained human labelers.
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Night of recording
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Collaborators and Investigators
Investigators
- Principal Investigator: Alexander Kain, Ph.D., Oregon Health and Science University
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB00008533
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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