NCT06378554

Cereset Research for Performance Improvement in a Hospital Nursing Unit

Enrolling by Invitation
NAAges 18+InterventionalSupportive care
Wake Forest University Health Sciences
~40 participants
Updated 2026-02-17 on ClinicalTrials.gov
What's tested:Cereset Research

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percent of ortho trauma unit staff who complete Cereset intervention
Measured over up to 2 years
Health Personnel
Stress
Anxiety
Insomnia
Depression
1 sites across 1 states
North Carolina1
  • Charles H Tegeler, MD · PRINCIPAL_INVESTIGATOR · Wake Forest University Health Sciences

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

Ability to comply with basic instructions and be able to sit still, comfortably during sessions.
Healthcare worker in the Orthopedic Trauma Unit at Atrium Health Wake Forest Baptist, aged 18 years and older.

Exclusion

Unable, unwilling, or incompetent to provide informed consent.
Physically unable to come to the study visits.
Severe hearing impairment (because CR involves acoustic stimulation that participants would need to be able to hear).
Weight is over the chair limit (400 pounds).
Currently enrolled in another Cereset Research study.
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). Individuals will be given the opportunity to discontinue these techniques for one month and then enroll.
Known seizure disorder.
Thoughts of active suicide within the last 3 months.
  • Percent of ortho trauma unit staff who complete Cereset interventionup to 2 years

    Percent of ortho trauma unit staff who complete CR Intervention