Status:
RECRUITING
Smart Pillows for Enhancing Sleep Quality
Lead Sponsor:
Indiana University
Conditions:
Snoring
Obstructive Sleep Apnea
Eligibility:
All Genders
50+ years
Phase:
NA
Brief Summary
The purpose of this study is to examine the impact of smart pillows on the sleep quality of individuals who experience a snoring issue and/or obstructive sleep apnea (OSA), as well as their sleep part...
Detailed Description
The study's timeline consists of 3 phases: * a pre-evaluation, or baseline, phase during the 7 days prior to study pillow use, * an intervention phase, occurring for 14 days during study pillow use, ...
Eligibility Criteria
Inclusion
- Inclusion criteria for individuals with snoring issues or OSA
- Individuals 50 years of age or older.
- Individuals who experience snoring issues and/or OSA that may impact their perceived sleep quality or that of their sleep partner.
- Individuals who currently use and do not use snoring and/or OSA treatment (participants will not be asked or required to discontinue any current snoring and/or OSA treatments that they are prescribed or using.)
- Individuals who have a smartphone or a smart mobile device (Apple iOS 15 and higher or Android 10 or higher).
- Individuals with and without a sleep partner.
- Individuals who do not have a pacemaker.
- Individuals who do not have intracranial electrodes.
- Individuals who do not have neck pain related to the cervical spine problems, including disc, muscle, and neurological issues.
- Inclusion criteria for sleep partners
- Individuals aged 18 years and older.
- Individuals who share the same sleeping space with their sleep partner (who has snoring issues and/or OSA) more than four times a week.
- Individuals whose sleep partner (who has snoring issues and/or OSA) agrees to participate in this study.
Exclusion
- Any participant who is not able to consent or complete study interventions independently, as determined by the investigator.
Key Trial Info
Start Date :
November 18 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 11 2026
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT06594627
Start Date
November 18 2024
End Date
July 11 2026
Last Update
August 29 2025
Active Locations (1)
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1
Indiana University
Indianapolis, Indiana, United States, 46202