Cereset Research for Performance Improvement in a Hospital Nursing Unit (NCT06378554) | Clinical Trial Compass
By InvitationNot Applicable
Cereset Research for Performance Improvement in a Hospital Nursing Unit
United States40 participantsStarted 2024-07-02
Plain-language summary
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.
Who can participate
Age range18 Years – 100 Years
SexALL
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Inclusion Criteria:
* 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 Criteria:
* 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.
What they're measuring
1
Percent of ortho trauma unit staff who complete Cereset intervention