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NCT06100185Recruiting

Wearable tES for Insomnia

Wearable Neurotechnology for Treatment of Insomnia (tES)
Uniformed Services University of the Health SciencesClinicalTrials.govdeviceDevice trial
Verified
Study focus
Disease/Condition
Insomnia
Drug/Device/Intervention
PeakSleep
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Uniformed Services University of the Health Sciences
Location
Bethesda, United States of America
Timeline & enrollment
Phase
N/A
Start date
Oct 25, 2023
End date
Sep 01, 2025
Enrollment
60 participants
Primary outcome

Sleep Onset Latency Change from Baseline

Summary

The purpose of this study is to investigate the ability of a translational device, Teledyne
 PeakSleep, to reduce sleep onset latency, reduce time awake after sleep onset and improve
 restfulness and the subjective benefits of sleep in a patient population with insomnia via
 transcranial direct current stimulation (tDCS) applied to frontal lobe circuits.

ICD-10 classifications
Nonorganic insomniaDisorders of initiating and maintaining sleep [insomnias]Sleep disordersSleep disorder, unspecifiedOther sleep disorders
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06100185
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06100185 through Pure Global AI's free database. This phase not specified trial is sponsored by Uniformed Services University of the Health Sciences and is currently Recruiting. The study focuses on Insomnia. Target enrollment is 60 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.