Status:

TERMINATED

Nextsense Brain-sensing Buds Study

Lead Sponsor:

NextSense, Inc.

Conditions:

Sleep

Sleep Quality

Eligibility:

All Genders

25-65 years

Phase:

NA

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...

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 ...

Eligibility Criteria

Inclusion

  • 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

  • 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.

Key Trial Info

Start Date :

October 7 2024

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 15 2025

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT06602960

Start Date

October 7 2024

End Date

April 15 2025

Last Update

April 18 2025

Active Locations (1)

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Alethios (Virtual Study Platform)

San Francisco, California, United States, 94109