At a glance
ClinicalIndex Comparison RecordN/ACompleted· 31 enrolled
Drug / intervention
Muse-S™ headband systemdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
MUSE Device to Improve Sleep Quality in Midlife Women
In Brief
A clinical study evaluating Muse-S™ headband system for Women's Health and 2 related conditions. Completed, enrolled 31 participants across 1 site.
Detailed Summary
The purpose of this study is to see if it is feasible for midlife women to wear a brain activity sensing headband (Muse-S) for management of sleep disturbances such as insomnia and sleep disruption
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsWomen's Health, Insomnia, Sleep Disturbance
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
202420252026
Enrollment StartAug 2023
First PostedAug 2023
Primary CompletionJan 2025
TodayJul 2026
First PostedAug 2, 2023
Enrollment StartAug 1, 2023
Primary CompletionJan 12, 2025
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 2.9 years ago
Interventions
Muse-S™ headband systemdevice
Clinical grade, headband-style wireless EEG (electroencephalogram is a test used to evaluate the electrical activity in the brain) system and designed to interact with a mobile device (a smartphone or tablet). The device is a soft, stretchy band that fits around the forehead to the back of the head.