- FDA-Approved At-Home Therapy
Proliv™Rx
- Understanding Proliv™Rx
What is Proliv™Rx?
Proliv™Rx is the first FDA-approved (Class II PMA), prescription, clinician-directed neuromodulation therapy that can be administered at home. It delivers focal, multi-channel, external Combined Occipital and Trigeminal Afferent Stimulation (eCOT-AS) through a non-invasive wearable headset.
The device applies gentle electrical pulses to targeted neural pathways associated with depression—without invasive procedures and with low risk of systemic side effects. At Resiliency Mind+Body Medicine®, we are proud to be part of the initial rollout of this groundbreaking therapy.
FDA-approved (Class II PMA) for MDD
At-home treatment under physician supervision
Non-invasive with low systemic side effects
App-guided with symptom tracking
At-Home
FDA-Approved Therapy
- The Challenge
When Antidepressants Aren't Enough
#1
Leading cause of disability globally
5%
Of US adults experience major depression
700K+
Annual suicide deaths worldwide
30%+
Show treatment resistance to antidepressants
$71B
Estimated annual economic burden in the US
- The Science
How Proliv™Rx Works
Trigeminal Stimulation
Forehead electrodes stimulate the supraorbital and supratrochlear trigeminal nerve branches bilaterally.
Occipital Stimulation
Rear electrodes stimulate the two greater occipital nerve branches at the back of the head.
Brainstem Pathway
Electrical pulses travel through sensory nerves to the brainstem, then into thalamo-cortical and limbic networks.
Mood Regulation
Signals modulate brain regions involved in mood, arousal, and autonomic regulation to alleviate depression.
- Your Journey
Clinician-Directed Care at Home
01
Prescribed by Clinician
Your physician evaluates your history and prescribes Proliv™Rx. The device is delivered to your home.
02
Self-Administer at Home
Wear the headset and follow app-based guidance for correct usage. Treatment is comfortable and non-invasive.
03
App-Guided Tracking
The companion app supports adherence, correct usage, and symptom tracking throughout your treatment.
04
Physician Monitoring
You remain under clinical supervision for ongoing monitoring, dose adjustments, and intervention as needed.
- Clinical Evidence
The MOOD Study
10.15
Point Reduction
On the Hamilton Depression Rating Scale (HDRS-17) in the active treatment group
32%
Full Remission
Of initially severe patients who previously failed antidepressants reached full remission (HDRS-17 ≤ 7)
56%
Mild or Depression-Free
At 16 weeks — compared to 0% at baseline. 81% were severe at baseline vs only 15% at 16 weeks.
Lead investigators include Dr. Linda Carpenter (Brown University) and Dr. Mark George (MUSC), among others from UCLA, Northwestern, UNC, and more.
- Candidacy
Is Proliv™Rx Right For You?
Antidepressant Non-Response
You've tried at least one antidepressant without adequate improvement in depression symptoms.
Occipital StimulationPrefer At-Home Treatment
You want an effective therapy you can do from home without frequent clinic visits.
Non-Invasive Option
You're looking for a non-invasive alternative with low risk of systemic side effects.
- The Resiliency Difference
Why Choose Resiliency for Proliv™Rx
Early Rollout Partner
We are part of the initial deployment of Proliv™Rx, bringing this breakthrough to our patients first.
Board-Certified Expertise
Led by Dr. LaFrenierre, double board-certified in Psychiatry and Addiction Medicine.
Integrated Treatment
Proliv™Rx alongside Deep TMS, Spravato, VNS, medication management, and lifestyle medicine.
Insurance Support
Our team assists with benefits verification and prior authorization to reduce barriers to care.
- Common Questions
Frequently Asked Questions
How is Proliv™Rx different from Deep TMS?
Do I still take my antidepressant medication?
What are the side effects?
When will Proliv™Rx be available?
Is Proliv™Rx covered by insurance?
Have more questions? Contact our clinical team.