Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
NCT06594627

Smart Pillows for Enhancing Sleep Quality

Led by Indiana University · Updated on 2025-08-29

24

Participants Needed

1

Research Sites

85 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Smart Pillows for Enhancing Sleep Quality

Who Can Participate

Age: 50Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals 50 years of age or older
  • Individuals who experience snoring issues and/or obstructive sleep apnea affecting sleep quality
  • Individuals currently using or not using snoring or OSA treatments
  • Individuals who have a smartphone or smart device with Apple iOS 15 or higher or Android 10 or higher
  • Individuals with or without a sleep partner
  • Individuals without a pacemaker
  • Individuals without intracranial electrodes
  • Individuals without neck pain from cervical spine problems including disc, muscle, or neurological issues
  • Sleep partners aged 18 years and older
  • Sleep partners who share the same sleeping space with the participant more than four times a week
  • Sleep partners whose participant agrees to join the study
Not Eligible

You will not qualify if you...

  • Anyone unable to consent or complete study procedures independently as judged by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Indiana University

Indianapolis, Indiana, United States, 46202

Actively Recruiting

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Research Team

C

Chang Dae Lee, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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