Facilitation Recovery For Patients With Chronic Stroke: The Q Therapeutic System, Frequency-Tuned Electromagnetic Field Treatment

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Evaluate the effectiveness of the Q Therapeutic (BQ 3.0) System for individuals with chronic stroke in improving upper extremity function as determined by change in functional outcome measures after 3-month treatment, including in-clinic and at-home sessions.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• FMA-UE score between 22-50 (inclusive) of impaired limb.

• Difference between Screening and Baseline visit FMA-UE is 3 points or fewer.

• Age 18 to 80 years of age (inclusive).

• Stroke due to ischemia or to intracerebral hemorrhage.

• \>6 months to 5 years from index stroke onset.

• Box \& Block Test score with affected arm is ≥1 block in 60 seconds at Baseline Visit.

• Able to sit with the investigational System for 40 consecutive minutes.

• Can follow a 3-step command, such as take the paper, fold it in half, and return it to me, or a non-verbal equivalent.

• Willingness to participate in physical exercises during study intervention sessions.

• Availability of a relative or other caregiver able to assist during study treatment sessions and visits.

• If female, not pregnant or breastfeeding or planning pregnancy during the study period.

• Informed consent signed by subject.

Locations
United States
New York
Burke Rehabilitation Hospital
RECRUITING
White Plains
Contact Information
Primary
Josette Hartnett, MPH
johartnett@burke.org
9145972367
Backup
Andrew Abdou, DO
aabdou@montefiore.org
7327137373
Time Frame
Start Date: 2025-05-26
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 25
Treatments
Experimental: BQ 3.0 Active Stimulation Group
60 sessions over a period of 12 weeks (5 treatments per week) of active study intervention with the BQ 3.0 (frequency and intensity parameters will be set to 1-100 Hz.; 0.1-1.0 G), including a standardized, pre-defined and evidence-based physical and occupational therapy regimen concurrent with the study intervention.
Related Therapeutic Areas
Sponsors
Leads: Burke Rehabilitation Hospital
Collaborators: BrainQ Technologies Ltd.

This content was sourced from clinicaltrials.gov