Cereset Research for Performance Improvement in a Hospital Nursing Unit

Enrolling by invitation · Not applicable

Conditions studied: Health Personnel, Stress, Anxiety, Insomnia, Depression

In brief

The purpose of this study is to explore whether an implementation process composed of offering CR to staff in a single hospital nursing unit has any potential impact on unit-level quality measures post-implementation.

Key facts

Study ID

NCT06378554

Run by

Wake Forest University Health Sciences

People needed

40

Starts

2024-07-02

Expected to finish

2027-07-01

Last updated by the study team

2026-02-17

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• Wake Forest University Health Sciences — Winston-Salem, North Carolina, United States

Full record on ClinicalTrials.gov

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