Fixed tES: Fixed stimulation parameters for all participants
Personalized tES: Stimulation parameters personalized for each participant
Study summary
The purpose of this study is to look at the effects of targeted brain stimulation when falling asleep and on sleep quality.
Eligibility
Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
Accepted
Inclusion Criteria:
* 18-75 year olds
Exclusion Criteria:
* Epilepsy
* Seizure History
* Serious head injury or brain surgery
* Migraines
* Metal implants in head
* Pacemaker or implanted devices
* Pregnancy
* Any serious medical condition other than insomnia
Primary outcome measure(s)
Sleep Efficiency Change — up to 6 weeks Sleep efficiency (time slept as a percentage time spent in bed) changes across the different interventions for each subject and aggregate that across subjects
Sleep Onset Change — 1 day to 6 weeks Changes in time to fall asleep across the different interventions for each subject and aggregate that across subjects
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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