Cereset for Health Care Workers

Recruiting in Palo Alto (17 mi)

Overseen byCharles H Tegeler, MD

Age: 18+

Sex: Any

Travel: May Be Covered

Time Reimbursement: Varies

Trial Phase: Academic

Waitlist Available

Sponsor: Wake Forest University Health Sciences

No Placebo Group

Trial Summary

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.

Eligibility Criteria

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.

+5 more

Participant Groups

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.

2Treatment groups

Active Control

Group I: Cereset Intervention GroupActive Control1 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 InterventionActive Control1 Intervention

No Intervention