NCT06594627 Smart Pillows for Enhancing Sleep Quality
| NCT ID | NCT06594627 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Indiana University |
| Condition | Snoring |
| Study Type | INTERVENTIONAL |
| Enrollment | 24 participants |
| Start Date | 2024-11-18 |
| Primary Completion | 2026-07-11 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 24 participants in total. It began in 2024-11-18 with a primary completion date of 2026-07-11.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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 partners. Furthermore, this study will explore whether enhancements in sleep quality positively influence depressive symptoms, physical activity, heart rate, blood oxygen levels, and cognitive functions.
Eligibility Criteria
Inclusion Criteria: * 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 Criteria: * Any participant who is not able to consent or complete study interventions independently, as determined by the investigator.
Contact & Investigator
Chang Dae Lee, PhD
PRINCIPAL INVESTIGATOR
Indiana University
Frequently Asked Questions
Who can join the NCT06594627 clinical trial?
This trial is open to participants of all sexes, aged 50 Years or older, studying Snoring. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06594627 currently recruiting?
Yes, NCT06594627 is actively recruiting participants. Contact the research team at cl150@iu.edu for enrollment information.
Where is the NCT06594627 trial being conducted?
This trial is being conducted at Indianapolis, United States.
Who is sponsoring the NCT06594627 clinical trial?
NCT06594627 is sponsored by Indiana University. The principal investigator is Chang Dae Lee, PhD at Indiana University. The trial plans to enroll 24 participants.