A Breakthrough Israeli Technology for Brain Rehabilitation

The neuroplastic helmet of BRAIN.Q enables an intensive daily brain rehabilitation process - from home, independently, at the time and pace suitable for each patient.

Approved for clinical use by the Ministry of Health.
Recognized by the U.S. FDA as a Breakthrough Device.
Clinical studies and collaborations with leading medical institutions worldwide.
Personalized adaptation and close clinical support for every patient.
Check Eligibility and Enroll →

Proud to collaborate with esteemed research and medical institutions

BRAIN.Q במהדורה המרכזית

קסדת השיקום המוחי בכתבת חדשות 12

פברואר 26׳
סרטון BRAIN.Q N12
Patients and Family Members Share

Behind the Numbers — People, Families, and Moments Restored.

“

I think that first and foremost, the close and encouraging support system after the initial rehabilitation was something my mother was really missing… There was no framework that could enable my mother to create a different reality for herself. It felt like the system was giving up on such a large segment of the population… I am keeping my fingers crossed that you will bring this kind of light to so many others.

Y., son of a patient
March 2026, Hadera
“

I really feel much stronger in my legs! I keep practicing many of these exercises because I feel that I am seeing results!

M., patient
May 2026, Rishon LeZion
“

BrainQ gave me something to look forward to every day.

K., participant in the EMAGINE study
“

I have to share because I’m in tears… For the first time, *** stood on his weaker leg (with the other leg on a step) without hand support. I was so excited that I forgot to take a video.

N., wife of a patient
May 2026, Netanya.
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Numbers That Tell a Story

The years, patients, and experience behind the platform.

4,200+
therapeutic sessions worldwide
4.8/5
patient satisfaction
90%
significant clinical improvement in functional independence
23
scientific publications

High Safety
No serious adverse events were reported throughout all clinical studies.

The findings are based on preliminary data from an ongoing clinical study. During the open-label phase (Day 90–180), participants received active treatment with the BRAIN.Q system up to five times per week. Improvement in functional status (mRS) was observed among participants who continued active treatment compared to those who did not.

The Core of the Program

The neuroplastic helmet is designed to support neuroplasticity processes.

The brain is our most valuable asset, and it operates through complex communication networks responsible for all our functions. Following a brain injury, such as a stroke, these networks may be damaged, leading to functional limitations. Brain rehabilitation and long-term brain health rely on the brain’s ability to reorganize itself through continuous learning and the creation of new patterns of activity within neural networks — a process known as neuroplasticity.
The system we developed at BRAIN.Q is designed to support and accelerate these processes. It is based on a personalized treatment approach centered around a helmet that generates a guided low-intensity electromagnetic field (Electromagnetic Network Targeting Field – ENTF), based on analysis of databases containing network-level brain activity from healthy individuals and people with brain injuries, using artificial intelligence.
The electromagnetic treatment is synchronized with a dedicated rehabilitation exercise program and a virtual monitoring and management platform, overseen by a clinician certified in the program. This combination is intended to maximize the potential impact on neural networks and encourage processes of reorganization (Neuroplasticity).
ערכת הטיפול של BRAIN.Q
The Patient’s Role in the Program

The Patient as a Leading and Active Partner in the Rehabilitation Process

Coping with a brain injury, such as a stroke, is a long and complex process that requires courage, determination, and a supportive environment. The program was built around the patient, based on an approach that sees the patient as an active partner and leader in their own rehabilitation journey.
The program combines advanced technology with continuous human support, with the goal of strengthening the patient’s sense of autonomy, capability, and confidence, while enabling both the patient and their loved ones to take an active role in long-term rehabilitation and ongoing brain health.
The system utilizes cloud technologies and artificial intelligence to enable daily multimodal treatment within the home environment, alongside continuous monitoring, personalization, and dynamic treatment management by an accompanying clinician throughout the journey.
This approach is based on well-established principles from rehabilitation and psychology, demonstrating that empowerment, active involvement, and daily experiences of success are key factors in persistence, functional improvement, and meaningful long-term rehabilitation — a process focused not only on reducing disability, but also on building vitality, joy, independence, and a return to an active routine.
Check Eligibility and Enroll →
אישה מבוגרת במהלך טיפול עם הקסדה האלקטרומגנטית
Checklist

Steps to Begin Home-Based Rehabilitation

1

Initial Conversation

2

Clinical Consultation Meeting

  • Independent clinical evaluation
  • Review of the medical profile for suitability to the program
  • The eligibility decision is made at the independent discretion of the physician
3

Contract Signing and Start Date Scheduling

If clinical eligibility is confirmed:

  • Contract signing
  • Scheduling a home setup appointment
4

Home Setup Meeting

  • A two-hour meeting with a clinician to adapt the program to the patient and family
  • Full training and delivery of the system to the patient
5

Program Initiation and Ongoing Support

  • Daily treatment guided by a dedicated clinician
  • Periodic evaluations
  • Ongoing adjustment of goals according to progress
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Personalized. Clinically Guided. Scientifically Proven.

  • Each patient receives close support from a personal treating clinician who has been carefully selected and specially trained on the system.
  • In a presentation at the World Stroke Congress* (2026), which analyzed the overall results of the company’s clinical studies, a significant contribution of the electromagnetic field to influencing brain networks and achieving consistent functional improvement over time was demonstrated.
  • The program is conducted in collaboration with leading neurological clinics in Israel.
  • The program is based on a decade of clinical research and development.
  • Continuous support enables dynamic adaptation of the program to each patient, as well as identification and resolution of challenges that arise along the way.
  • The program is supervised by BRAIN.Q’s Medical Director, Dr. Jeffrey Saver, Director of the Stroke Center at UCLA and a world-renowned neurologist.

*The data are based on randomized controlled trials (RCTs) involving patients with moderate-to-severe subacute ischemic stroke.

*הנתונים מבוססים על מחקרים אקראיים מבוקרים (RCT) בקרב מטופלים עם שבץ איסכמי בינוני–קשה בשלב הסאב־אקוטי.

Dr. Jeffrey Saver
BRAIN.Q Medical Director
Launch Pricing

Program Cost

One-time setup fee
2,000 ILS
Monthly payment
2,500 ILS
The monthly fee includes the loan of the system for home use, together with a closely supervised clinical support framework accompanying the patient throughout the entire process.
As the program focuses on creating meaningful functional change, it is recommended to continue the process for at least six months, subject to clinical evaluation and improvement in the patient’s condition.
Check Eligibility and Enroll →
זוג מבוגר בחוף הים