NCT01680380

Brief Summary

The purpose of this study is to evaluate the feasibility of tracking breathing during sleep with non-contact sensors (for example, microphones or wireless movement sensors). The investigators will use the data collected with these sensors to develop algorithms for tracking breathing during sleep. The investigators will assess the performance of the algorithms by comparing automatic output against manually-generated labels.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Oct 2012

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 4, 2012

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 7, 2012

Completed
24 days until next milestone

Study Start

First participant enrolled

October 1, 2012

Completed
3.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2016

Completed
Last Updated

July 7, 2016

Status Verified

July 1, 2016

Enrollment Period

3.8 years

First QC Date

September 4, 2012

Last Update Submit

July 5, 2016

Conditions

Keywords

sleep apneasnoring

Outcome Measures

Primary Outcomes (1)

  • Breathing sounds are evident in overnight audio recordings

    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.

    Night of recording

Study Arms (1)

At-Home

Overnight sleep at home

Eligibility Criteria

Age21 Years - 89 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Participants will be recruited from the PI's department (OHSU faculty, Ph.D. students) by email and the investigators' personal acquaintances. Participants must be age 21-100 and have no self-reported sleep breathing problems.

You may qualify if:

  • Age 21-89
  • No self-reported sleep breathing problems

You may not qualify if:

  • Positive diagnosis for sleep breathing problem (e.g., obstructive sleep apnea)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Center for Spoken Language Understanding

Portland, Oregon, 97239, United States

Location

MeSH Terms

Conditions

Sleep Apnea SyndromesSnoring

Condition Hierarchy (Ancestors)

ApneaRespiration DisordersRespiratory Tract DiseasesSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesRespiratory SoundsSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Alexander Kain, Ph.D.

    Oregon Health and Science University

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

September 4, 2012

First Posted

September 7, 2012

Study Start

October 1, 2012

Primary Completion

August 1, 2016

Study Completion

August 1, 2016

Last Updated

July 7, 2016

Record last verified: 2016-07

Locations