Cereset for Health Care Workers

Overseen By Charles H Tegeler, MD

Age: 18+

Sex: Any

Trial Phase: Academic

Sponsor: Wake Forest University Health Sciences

Disqualifiers: Severe hearing impairment, Seizure disorder, Suicide thoughts, others

No Placebo Group All trial participants will receive the active study treatment (no placebo)

Compensation: Varies

Number of Visits: 4

40 Participants Needed

What You Need to Know Before You Apply

What is the purpose of this trial?

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.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. However, if you are using certain brain stimulation or therapy techniques, you must stop them for one month before joining the study.

Who Is on the Research Team?

Charles H Tegeler, MD

Principal Investigator

Wake Forest University Health Sciences

Are You a Good Fit for This Trial?

This trial is for healthcare workers in a hospital nursing unit who may be experiencing anxiety, stress, depression, sleep disorders or insomnia. Specific eligibility criteria are not provided.

Inclusion Criteria

I am an adult working in the Orthopedic Trauma Unit at Atrium Health Wake Forest Baptist.

Ability to comply with basic instructions and be able to sit still, comfortably during sessions

Exclusion Criteria

Severe hearing impairment (because CR involves acoustic stimulation that participants would need to be able to hear)

Currently enrolled in another Cereset Research study

I am unable to give informed consent.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Implementation

Implementation of the Cereset Research intervention among nursing unit staff

4 sessions

4 visits (in-person)

Post-implementation Evaluation

Evaluation of individual-level behavioral symptoms and nursing performance metrics post-intervention

up to 2 years

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

• Cereset Research

Trial Overview The study is testing the impact of Cereset Research (CR) on quality measures within a single hospital nursing unit after it's offered to staff members.

How Is the Trial Designed?

Group I: Cereset Intervention Group Active Control 1 Intervention

This system uses the same core technology and algorithms to echo brainwaves in real-time using audible tones, as with High-resolution, relational, resonance-based, electroencephalic mirroring (HIRREM).

Group II: No Intervention Active Control 1 Intervention

No Intervention

Who Is Running the Clinical Trial?

Wake Forest University Health Sciences

Lead Sponsor

Trials

1,432

Recruited

2,506,000+

Susanne Marcus Collins Foundation, Inc.

Collaborator

Trials

2

Recruited

130+

The Susanne Marcus Collins Foundation, Inc.

Collaborator

Trials

5

Recruited

430+