Q Therapeutic System for Chronic Stroke Recovery

Part of paid clinical trials in White Plains, New York.

Sponsor
Burke Rehabilitation Hospital
Study ID
NCT06979466
Status
Recruiting

Conditions

  • Brain Injury
  • Cerebrovascular Accident (CVA)
  • Chronic Stroke Patient
  • Hemorrhage
  • Stroke

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • Q Therapeutic System (BQ 3.0) - Active — DEVICE
    The BQ 3.0 is a medical device that produces and delivers non-invasive, extremely low intensity and frequency (1-100 Hz.; 0.1-1.0 G), frequency tuned electromagnetic fields in order to stimulate neuronal networks with the aim of reducing disability and promoting neurorecovery

Study Details

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.

Key Dates

Start date
May 26, 2025
Status verified
Aug 2025
Primary completion
May 31, 2026
Completion
Jun 30, 2026

Study Design

Enrollment
25 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • 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.

Primary Outcome Measure

Fugl-Meyer Assessment - Upper Extremity [ Time Frame: Baseline, 3 month, 5 month, 6 month ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Burke Rehabilitation HospitalWhite PlainsNew York10605
Josette Hartnett, MPH
9142756481
Andrew Abdou, DO
7327137373
Andrew Abdou, DO (PRINCIPAL_INVESTIGATOR)
Mooyeon Oh-Park, MD, MHCM (SUB_INVESTIGATOR)

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