RECRUITING

Smart Pillows for Enhancing Sleep Quality

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Smart Pillows for Enhancing Sleep Quality_Pilot Study

Quick Facts

Study Start:2024-11-18
Study Completion:2025-07-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06594627

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Inclusion criteria for individuals with snoring issues or OSA
  2. * Individuals 50 years of age or older.
  3. * Individuals who experience snoring issues and/or OSA that may impact their perceived sleep quality or that of their sleep partner.
  4. * 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.)
  5. * Individuals who have a smartphone or a smart mobile device (Apple iOS 15 and higher or Android 10 or higher).
  6. * Individuals with and without a sleep partner.
  7. * Individuals who do not have a pacemaker.
  8. * Individuals who do not have intracranial electrodes.
  9. * individuals who do not have cervical spine problems, including disc, muscle, and neurological issues.
  10. * Individuals aged 18 years and older.
  11. * Individuals who share the same sleeping space with their sleep partner (who has snoring issues and/or OSA) more than four times a week.
  12. * Individuals whose sleep partner (who has snoring issues and/or OSA) agrees to participate in this study.
  1. * Any participant who is not able to consent or complete study interventions independently, as determined by investigator.

Contacts and Locations

Study Contact

Chang Dae Lee, PhD
CONTACT
317-274-5365
cl150@iu.edu

Principal Investigator

Chang Dae Lee, PhD
PRINCIPAL_INVESTIGATOR
Indiana University

Study Locations (Sites)

Indiana University
Indianapolis, Indiana, 46202
United States

Collaborators and Investigators

Sponsor: Indiana University

  • Chang Dae Lee, PhD, PRINCIPAL_INVESTIGATOR, Indiana University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-11-18
Study Completion Date2025-07-11

Study Record Updates

Study Start Date2024-11-18
Study Completion Date2025-07-11

Terms related to this study

Keywords Provided by Researchers

  • assistive device
  • sleep quality
  • snoring
  • obstructive sleep apnea

Additional Relevant MeSH Terms

  • Snoring
  • Obstructive Sleep Apnea