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Clinical Trials/NCT06602960
NCT06602960
Terminated
Not Applicable

Nextsense Brain-sensing Buds Study

NextSense, Inc.1 site in 1 country40 target enrollmentOctober 7, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sleep
Sponsor
NextSense, Inc.
Enrollment
40
Locations
1
Primary Endpoint
Participant-reported Sleep Quality
Status
Terminated
Last Updated
last year

Overview

Brief Summary

The purpose of this clinical trial is to explore how the presentation of sleep data impacts sleep quality, sleep-related behaviors (such as sleepiness), and sleep-related anxiety and stress. The study aims to answer the following key questions:

  1. Does receiving sleep-related feedback from a wearable sleep tracker affect an individual's mindset about sleep?
  2. How does the mindset about sleep influence sleep quality, sleepiness, and stress/anxiety levels related to sleep?
  3. Does the feedback on sleep data moderate the relationship between one's mindset about sleep and their sleep quality?

Participants will:

  1. Be randomly assigned to receive different types of feedback about their sleep data to determine if the way sleep data is presented influences self-reported sleep quality, sleepiness, and sleep-related stress.
  2. During the baseline period (Weeks 1-2), complete daily and weekly surveys assessing their sleep habits, beliefs about sleep, anxiety, stress, and mindset regarding sleep.
  3. For Weeks 3-4, wear a Fitbit and Brain-Sensing earbuds, receiving daily feedback on their sleep.
  4. At the end of the study, provide feedback on their experience using the devices. Participants may choose to return the devices or keep them after the study concludes.

Detailed Description

With the growing prevalence of sleep-tracking wearables available to consumers, understanding the psychological and behavioral impacts they have on users is important. Recent advancements in wearable technology allow for monitoring various sleep parameters, providing users with extensive data on their sleep patterns. The study aims to examine how the presentation of sleep data influences user sleep quality, sleep-related behaviors, including sleepiness, and sleep-related anxiety and stress. It will evaluate how the presentation of sleep data affects individuals\' perceptions of sleep and related health issues, including daytime sleepiness and perceived sleep quality. Participants will receive sleep data feedback based on new methods assessed using Fitbit, brain-sensing earbuds, and other factors that might impact sleep. Additionally, the study seeks to offer valuable insights into sleep research, behavioral psychology, and wearable technology.

Registry
clinicaltrials.gov
Start Date
October 7, 2024
End Date
April 15, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All participants have the capacity to understand the informed consent for study participation and ability for subject to comply with the requirements of the study
  • Experiencing mild to moderate sleep disturbances, but without sleep disorder diagnosis
  • Naïve to sleep tracker use
  • Age 25-65

Exclusion Criteria

  • Participants who have used any type of sleep tracker, such as Oura, Fitbit, Google Fit, Garmin Connect, or Apple Watch Sleep
  • Health conditions (i.e., cancer, cognitive impairment, panic disorder, post-traumatic stress disorder, sleep apnea, insomnia, restless leg syndrome, Parkinson's disease)
  • Use of Modafinil (Provigil), Methylphenidate (Ritalin), Sodium oxybate (Xyrem), Melatonin, Benadryl, Wakix, Sunosi or prescription medications for ADHD Enrollment in other sleep studies
  • Women who are pregnant or who are currently nursing/breastfeeding will be excluded from this study.

Outcomes

Primary Outcomes

Participant-reported Sleep Quality

Time Frame: 4 weeks (Week 1 - Week 4): measured at baseline, in daily surveys.

Measured via self-report using the 15-item Groningen Sleep Quality Scale, with scores ranging from 1 to 14. A score of 14 indicates poor sleep quality the previous night.

Sleep data - Total hours of sleep

Time Frame: 2 weeks (Week 3 - Week 4): measured daily, sleep data tracked by Fitbit will be transmitted to the Alethios platform automatically once a day.

Total hours of sleep data tracked by Fitbit

Modified Karolinska Sleepiness Scale

Time Frame: 4 weeks (Week 1 - Week 4): measured at baseline, in daily surveys.

Sleepiness, measured via self-report using the 1-item modified Karolinska Sleepiness Scale, ranges from 1 to 10, with 1 indicating extreme alertness, 3 alert, 5 neither alert nor sleepy, 7 sleepy but no difficulty remaining awake, 9 extremely sleepy, fighting sleep, and 10 extremely sleepy, falling asleep all the time.

Fitbit tracked Sleep Quality

Time Frame: 2 weeks (Week 3 - Week 4): measured daily, sleep data tracked by Fitbit will be transmitted to the Alethios platform automatically once a day.

Fitbit sleep score, ranging from 0 to 100, indicates sleep quality: 90-100 is excellent, 80-89 good, 60-79 fair, and 0-59 poor, based on duration, disturbances, and restorative sleep.

Secondary Outcomes

  • Anxiety, Stress, and Mindset related to Sleep(4 weeks (Week 1 - Week 4): measured at baseline, in weekly surveys.)
  • Dysfunctional Beliefs and Attitudes about Sleep 16-item(4 weeks (Week 1 - Week 4): measured at baseline, in weekly surveys.)
  • Modified Insomnia Severity Index(Week 2 and Week 4: measured twice.)
  • Satisfaction with sleep(Week 2 and Week 4: measured twice.)
  • Sleep Problems Interference with Daily Functioning(Week 2 and Week 4: measured twice.)
  • Pre-Sleep Arousal Scale(4 weeks (Week 1 - Week 4): measured at baseline, in weekly surveys.)

Study Sites (1)

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