Cereset Research Long-Term Healthcare Worker Study (LT-HW)
Stress, Anxiety, Autonomic Dysregulation
About this trial
This is an interventional supportive care trial for Stress focused on measuring stress, anxiety, insomnia, Cereset Research, hyperarousal, brain electrical activity, autonomic dysregulation, neurotechnology, HIRREM, allostasis, neuromodulation, acoustic stimulation, COVID-19, healthcare worker
Eligibility Criteria
Inclusion Criteria: Employed healthcare workers aged 18 years and older. Have availability and interest in participating in a 1 year study. Ability to comply with basic instructions and be able to sit still, comfortably during sessions. Experiencing symptoms of stress meeting threshold score on the Perceived Stress Scale (PSS ≥ 14). Exclusion Criteria: No internet access, as some visits collected electronically Unable, unwilling, or incompetent to provide informed consent. Physically unable to come to the study visits, or to sit still, comfortably in a chair for up to 1 hour. Severe hearing impairment (because the subject will be using ear buds during CR). Weight is over the chair limit (400 pounds). Currently enrolled in another active intervention research study. Prior use of: HIRREM, HIRREM-SOP, Brainwave Optimization (BWO), Cereset, Cereset Research, Cereset Home, or a wearable configuration of the same (B2, or B2v2). Prior use of the following modalities within one month before enrollment: electroconvulsive therapy (ECT), prior use of transcranial magnetic stimulation (TMS), transcranial direct current stimulation (TDCS), alpha stimulation, eye movement desensitization and reprocessing (EMDR), brain spotting, neurofeedback, biofeedback, or deep brain stimulation (DBS). Known seizure disorder. Thoughts of active suicide within the last 3 months. Current medical student.
Sites / Locations
- Atrium Wake Forest Baptist Health
Arms of the Study
Arm 1
Arm 2
Active Comparator
Other
Cereset Research Tune-Up Intervention Group
Cereset Research Control Group
All study participants will receive 4 initial CR sessions. Afterwards, they will be randomized, and this group will receive an additional tune-up (maintenance) session every 6 weeks for one year. There will be a CR session at weeks 6, 12, 18, 24, 30, 36, 42, and 48.
All study participants will receive 4 initial CR sessions. Afterwards, they will be randomized, and this group will continue their current care for 1 year with no additional CR sessions.