No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
40 – 80
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
12 (estimated)
Sponsor
Wake Forest University Health Sciences · Other
Who this trial is looking for
This trial is looking for adults with moderate depression who want to improve their deep sleep. Participants will wear a device that records brain activity and provides electrical stimulation during sleep, while also completing sleep and mood questionnaires.
Are You a Good Fit for This Trial?
Rules you outSubstance use disorderCurrent suicidal ideationSevere insomniaSevere untreated sleep apneaPregnancy
You may be able to join if
I can complete an overnight sleep study with EEG leads.
I can read and understand English.
I have moderate depression.
I have self-reported cognitive complaints.
You may not be able to join if
I have had a bad reaction to brain stimulation before.
I have any implanted devices in my head.
I have metal in my head.
I am allergic to silver.
I have a significant neurologic disease.
I have a history of significant head trauma.
I have a history of stroke or other ischemic events.
I have been diagnosed with schizophrenia or bipolar disorder.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The goal of this pilot study is to determine if non-invasive brain stimulation during sleep can increase deep sleep in adults with depression. It will also determine if increased deep sleep improves cognitive performance and mood ratings. Participants will be asked to wear a non-invasive device that records their brain activity and delivers transcranial electrical stimulation during sleep. Partici…
The goal of this pilot study is to determine if non-invasive brain stimulation during sleep can increase deep sleep in adults with depression. It will also determine if increased deep sleep improves cognitive performance and mood ratings. Participants will be asked to wear a non-invasive device that records their brain activity and delivers transcranial electrical stimulation during sleep. Participants will also wear an actigraphy watch that measures activity levels throughout the study. In addition, participants will complete several cognitive assessments and mood and sleep questionnaires throughout the study.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Ability to complete overnight sleep study including placement of EEG leads
* Ability to read and understand English.
* Moderate depression
* Self-reported cognitive complaints
Exclusion Criteria:
* Previous adverse reaction to transcranial electrical stimulation
* Presence o…
Inclusion Criteria:
* Ability to complete overnight sleep study including placement of EEG leads
* Ability to read and understand English.
* Moderate depression
* Self-reported cognitive complaints
Exclusion Criteria:
* Previous adverse reaction to transcranial electrical stimulation
* Presence of implanted devices (e.g. intracranial device, cochlear implant)
* Presence of metal in head (e.g. surgical clip)
* Sensitivity or allergy to silver
* Presence of significant neurologic disease (e.g. Parkinson's disease, epilepsy/seizure disorder, severe migraine disorder)
* History of significant head trauma
* History of stroke or other ischemic event
* Diagnosed with schizophrenia, bipolar disorder, substance use disorder, or presence of current suicidal ideation
* Currently taking medications that could alter EEG or cognitive function
* Presence of severe insomnia
* Presence of severe, untreated sleep apnea
* Currently pregnant
* Planned travel outside time zone during the study
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