HIRREM Hot Flashes Study

Wake Forest University (WFU)

Status: Completed

Conditions: Menopause; Hot Flashes; Vasomotor Symptoms

Treatments: Other: Continued Current Care; Device: HIRREM

Study type: Interventional

Funder types: Other

Identifiers

NCT03512002

IRB00049252

Details and patient eligibility

About

The purpose of this research study is to determine the effects of a technique called High-resolution, relational, resonance-based, electroencephalic mirroring (HIRREM®), for women in any stage of menopause, who are experiencing menopause-related hot flashes.

Full description

The purpose of this research study is to determine the effects of a technique called High-resolution, relational, resonance-based, electroencephalic mirroring (HIRREM®), for hot flashes. HIRREM uses scalp sensors to monitor brain electrical activity, and computer software algorithms translate selected brain frequencies into audible tones in real time. Those tones are reflected back to participants via ear buds in as little as four to eight milliseconds, providing the brain an opportunity for self-adjustment of its electrical pattern.

This study will compare acoustic stimulation linked to brainwave activity (HIRREM, along with continued current care, HCC), with continued current clinical care alone (CCC). Both groups will continue their other current care throughout, including non-pharmacological, and lifestyle modification therapies.

Enrollment: 8 patients

Sex: Female

Ages: 40+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Women, age 40 and above
• Intact uterus and ovaries
• Have at least 5 hot flashes per day (with at least one being categorized as moderate to severe, in a stable pattern for one month).

Exclusion criteria

• Less than 5 hot flashes per day
• Does not experience at least 1 moderate to severe hot flash per day
• Unable, unwilling, or incompetent to provide informed consent
• Physically unable to come to the study visits, or to sit comfortably in a chair for up to two hours
• Known seizure disorder
• Known or potential pregnancy (females with last menstrual period less than one year from enrollment will be tested for pregnancy prior to randomization)
• Severe hearing impairment (because the subject will be using headphones during the interventions)
• Ongoing need for treatment with opiate, benzodiazepine, or anti-psychotic medications, anti-depressant medications such as SSRI, SNRI, or tricyclic, and sleep medications such as zolpidem or eszopiclone
• Use of pharmaceuticals for treatment of vasomotor symptoms or any type of hormone replacement therapy
• Use of supplements for improvement of vasomotor symptoms including but not limited to black cohosh, soy isoflavone extract, and red clover leaf extract
• Menopausal symptoms resulting from, or associated with surgery, chemotherapy, radiation, or use of other chemicals or medications
• Anticipated and ongoing use of recreational drugs, alcohol, or energy drinks
• Ongoing need for treatment with thyroid medications
• Weight is over the chair limit (285 pounds)
• Are enrolled in another research study that includes an active intervention
• Have previously received brainwave optimization (BWO), used a B2 or a B2v2 wearable device, or previously participated in a HIRREM research study

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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8 participants in 2 patient groups

HIRREM

Active Comparator group

Description:

High-resolution, relational, resonance-based, electroencephalic mirroring (HIRREM) is a novel, noninvasive, closed-loop, brainwave mirroring, acoustic stimulation neurotechnology to support relaxation and auto-calibration of neural oscillations, using auditory tones to reflect brain frequencies in near real time.

Treatment:

Other: Continued Current Care

Device: HIRREM

Continued Current Care

Other group

Description:

Participants will continue their current care.

Treatment:

Other: Continued Current Care

Device: HIRREM