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Behavioural Intervention
EMBr Wave Device for Hot Flashes in Breast Cancer Survivors
N/A
Waitlist Available
Led By Sagar Sardesai, MBBS
Research Sponsored by Ohio State University Comprehensive Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Women with history of breast cancer, ductal breast carcinoma in situ (DCIS), or lobular breast carcinoma in situ (LCIS) (currently without evidence of malignant disease)
Presence of hot flashes for > 30 days prior to study entry
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 8 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial studies how well the EMBr Wave device works in reducing hot flashes in women with a history of breast cancer. These women cannot use hormone replacement therapy, so the device offers an alternative by providing heating or cooling sensations on the wrist to manage hot flashes.
Who is the study for?
This trial is for women with a history of breast cancer who experience frequent hot flashes (at least 28 times per week) and are not currently undergoing certain cancer treatments. Participants must be willing to wear the EMBr Wave device, use its mobile app, have a smartphone compatible with the app, and have an ECOG performance status of 0 or 1.
What is being tested?
The study tests if the EMBr Wave device can reduce hot flash severity in women who've had breast cancer. The wearable tech aims to provide relief without hormones by heating or cooling at the wrist. Participants will also complete questionnaires about their experiences.
What are the potential side effects?
Potential side effects are not detailed for this trial; however, since it involves wearing a non-invasive device on the wrist, risks may be minimal compared to drug therapies. Users should monitor for any skin irritation or discomfort due to wearing the device.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I had breast cancer or a non-invasive breast condition but currently show no signs of cancer.
Select...
I have been experiencing hot flashes for more than 30 days.
Select...
I am fully active or have some restrictions but can still care for myself.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 8 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 8 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Device usage
Patient satisfaction
Secondary study objectives
Effect of EMBr Wave using Hot Flash-Related Daily Interference Scale (HFRDIS)
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Arm A (EMBr Wave)Experimental Treatment2 Interventions
Patients utilize the EMBr Wave device for 4 weeks, then crossover to arm B for 4 weeks.
Group II: Arm B (crossover)Active Control2 Interventions
Patients receive no treatment for 4 weeks, then crossover to arm A for 4 weeks.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Hot flashes are commonly treated with hormone therapy, which works by supplementing estrogen to stabilize the body's thermoregulatory center in the hypothalamus. Nonhormonal treatments, such as selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs), modulate neurotransmitters to help regulate body temperature.
The EMBr Wave device, a nonhormonal option, uses thermal regulation by providing controlled heating and cooling sensations to the wrist, which can help manage the body's perception of temperature changes. This is particularly important for patients who cannot use hormone therapy due to contraindications, such as a history of breast cancer, offering them a safe and effective alternative for managing hot flashes.
Is placebo as effective as estrogen regimens on vasomotor symptoms in women with surgical menopause?Vasomotor symptoms in menopause: physiologic condition and central nervous system approaches to treatment.Estrogen with and without progestin: benefits and risks of short-term use.
Is placebo as effective as estrogen regimens on vasomotor symptoms in women with surgical menopause?Vasomotor symptoms in menopause: physiologic condition and central nervous system approaches to treatment.Estrogen with and without progestin: benefits and risks of short-term use.
Find a Location
Who is running the clinical trial?
Ohio State University Comprehensive Cancer CenterLead Sponsor
340 Previous Clinical Trials
294,200 Total Patients Enrolled
Embr Labs, Inc.Industry Sponsor
2 Previous Clinical Trials
80 Total Patients Enrolled
Sagar Sardesai, MBBSPrincipal InvestigatorOhio State University Comprehensive Cancer Center
1 Previous Clinical Trials
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am currently on, or plan to start, androgen therapy within 4 weeks.I had breast cancer or a non-invasive breast condition but currently show no signs of cancer.You have used EMBr Wave before.I am currently undergoing or planning to start chemotherapy within 4 weeks, but treatments targeting HER2 are okay.I have been on a stable dose of Tamoxifen, Raloxifene, or an aromatase inhibitor for at least 4 weeks.I have taken or plan to take Clonidine in the last 4 weeks.You are allergic to nickel.I experience severe hot flashes more than 28 times a week.I have been experiencing hot flashes for more than 30 days.I've been using local estrogen for vaginal atrophy for over 28 days without plans to change.I am using or plan to use gabapentin/pregabalin for hot flashes, not for pain.I am willing to use the EMBr Wave app.I am currently taking or plan to take progestogens.I am taking SSRIs or SNRIs for depression or hot flashes and won't change the dose during the study.I am fully active or have some restrictions but can still care for myself.You are expected to live for at least 6 more months.
Research Study Groups:
This trial has the following groups:- Group 1: Arm A (EMBr Wave)
- Group 2: Arm B (crossover)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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