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Completed Not applicable Interventional

The Efficacy of a Frequency-tuned Electromagnetic Field Treatment in Facilitating the Recovery of Subacute Ischemic Stroke Patients - a Pivotal Study (THE "EMAGINE" STUDY)

ClinicalTrials.gov ID: NCT05044507

Public ClinicalTrials.gov record NCT05044507. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 9, 2026, 3:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multicenter study that will be conducted at approximately 20 centers. BQ 2.0 is a wearable medical device that produces and delivers non-invasive, extremely-low-intensity and low-frequency, frequency-tuned electromagnetic fields in order to stimulate neuronal networks with the aim of reducing disability and promoting neurorecovery. In this study, BQ 2.0 is intended to reduce disability in adult patients with subacute ischemic stroke, with a moderate to severe disability which includes an upper extremity motor impairment. BQ 2.0 will be used for 9 weeks in conjunction with physical and occupational therapy (PT/OT) and periodic supervision (either remote or in person) of a trained site study team member. Treatments may be administered in multiple settings (e.g. acute care hospital (ACH) or inpatient rehabilitation facilities (IRF), Skilled Nursing Facility (SNF), home or other outpatient setup). The study will enroll up to 150 adult subjects who will be randomly assigned (1:1 allocation ratio) to either active or sham study intervention using BQ 2.0.

Study identification

NCT ID
NCT05044507
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
BrainQ Technologies Ltd.
Industry
Enrollment
100 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
22 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 3, 2021
Primary completion
Nov 5, 2023
Completion
Jan 15, 2024
Last update posted
Mar 18, 2024

2021 – 2024

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
Rancho Research Institute Downey California 90242
Ronald Reagan UCLA Medical Center & California Rehabilitation Institute Los Angeles California 90095
MedStar National Rehabililtaion Hospital, Washington D.C. District of Columbia 20010
Brooks Rehabilitation Hospital - University Campus Jacksonville Florida 32216
The Miami Project to Cure Paralysis Miami Florida 33136
Shirley Ryan Abilitylab Chicago Illinois 60611
KU Medical Center Kansas City Kansas 66160
Spaulding Rehabilitation Hospital Boston Massachusetts 02129
JFK Johnson Rehabilitation Institute Edison New Jersey 08820
Kessler Institute of Rehabilitation West Orange New Jersey 07052
NYP Brooklyn Methodist Hospital Outpatient Rehabilitation Brooklyn New York 11215
Atrium Health Carolinas Rehabilitation Charlotte North Carolina 28203
Moss Rehabilitation Research Institute Elkins Park Pennsylvania 19027
Baylor Scott & White Institute for Rehabilitation Dallas Texas 75246
TIRR Memorial Hermann Hospital Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05044507, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 18, 2024 · Synced Sep 9, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05044507 live on ClinicalTrials.gov.

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