Cereset Research Exploratory Study
Recruiting now · Not applicable
Conditions studied: Neurological Diseases or Conditions, Cardiovascular Conditions After Birth, Psychophysiologic Disorders
In brief
The purpose of this study is to evaluate the use of Cereset Research to improve autonomic function in participants with symptoms of stress, anxiety, or insomnia.
Key facts
- Study ID
- NCT03777267
- Run by
- Wake Forest University Health Sciences
- People needed
- 200
- Starts
- 2019-04-12
- Expected to finish
- 2028-04-01
- Last updated by the study team
- 2026-07-20
Who can join
Age: 11 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects must have the ability to comply with basic instructions and be able to sit still comfortably with the sensor leads attached
- Subjects experiencing symptoms of stress, anxiety, or insomnia, who meet threshold scores on one or more self-reported inventories for the same. This includes the Insomnia Severity Index (ISI, ≥ 8), the Perceived Stress Index (PSS, ≥ 14), or the Generalized Anxiety Disorder 7-item (GAD-7, ≥ 5) scale.
You may not qualify if…
- Unable, unwilling, or incompetent to provide informed consent/assent.
- Physically unable to come to the study visits, or to sit comfortably in a chair for up to 1.5 hours.
- Severe hearing impairment (because the subject will be using ear buds during CR).
- Weight is over the chair limit (285 pounds).
- Currently in another active intervention research study.
- Prior use of HIRREM, Brainwave Optimization, Cereset, or a wearable configuration of the same (B2, or B2v2) within the last 3 years.
- Prior use of electroconvulsive therapy (ECT).
- Prior use of transcranial magnetic stimulation (TMS), transcranial direct current stimulation (TDCS), alpha stimulation, neurofeedback, biofeedback, or deep brain stimulation (DBS) within one month before enrollment.
- Known seizure disorder.
Where it is running
- Wake Forest University Health Scienc\ess — Winston-Salem, North Carolina, United States (enrolling)
Full record on ClinicalTrials.gov
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