White Plains, NYNCT06979466Now EnrollingIRB Ready

Stroke Clinical Trial in White Plains, NY

Access cutting-edge stroke treatment through this clinical trial at a research site in White Plains. Study-provided care at no cost to qualified participants.

Sponsored by Burke Rehabilitation Hospital

Quick Self-Assessment

See if you qualify for this White Plains location

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Expert Care in White Plains

Access stroke specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related stroke treatment provided free

Apply for This White Plains Location

Check if you qualify for this stroke clinical trial in White Plains, NY

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to White Plains

    Convenient for NY residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit White Plains site if eligible
  4. 4Begin participation

About This Stroke Study in White Plains

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.

Sponsor: Burke Rehabilitation Hospital

Who Can Participate

Inclusion Criteria

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.

Exclusion Criteria

Severe neglect impairment interfering with assessments or treatments.
Severe depression, defined as GDS Score \>10/15
The presence of MR-incompatible implanted devices or MR-incompatible retained objects; or the presence of life-sustaining MR-compatible devices (e.g. pacemaker or internal cardiac defibrillator).
Active epilepsy or currently taking anti-epileptic medication (indicated for the treatment of a seizure disorder), or any epileptic seizure in the last 5 years
Botulinum toxin to the paretic arm: received in the prior 3 months OR expected before the 6-Month Visit
Severe UE spasticity, defined as presence of upper extremity contracture or modified Ashworth Scale score≥3 in either biceps or pectoralis
Pre-existing neurological condition (eg, Alzheimer's disease, Parkinson's disease, multiple sclerosis, traumatic brain injury, spinal cord injury) or physical limitation that would interfere significantly with the subject's participation in the study and/or confound neurological or functional evaluation.
Significant visual disturbances, pre-existing or resulting from the index stroke, that cannot be corrected and that would interfere significantly with the subject's participation in the study and/or confound neurological or functional evaluation.
Unstable serious illness/condition (eg, active cancer, severe heart failure, active major psychiatric condition) or life expectancy of less than 12 months.
Alcohol abuse and/or illicit drug abuse in the past 6 months, which is likely to influence ability to fully participate in the trial.
Participation in another interventional trial that would conflict with the current study or clinical endpoint interference may occur.
Participation in an upper extremity rehabilitation program provided by a licensed provider in the 4 weeks prior to the Screening visit, or a or planned participation in such program at any time between the Screening Visit and the primary endpoint visit.
Employee of the Sponsor.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in White Plains?

Yes, this clinical trial (NCT06979466) has an active research site in White Plains, NY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Stroke Treatment Options in White Plains, NY

If you're searching for stroke treatment options in White Plains, NY, this clinical trial (NCT06979466) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our White Plains research site is actively enrolling participants for this clinical trial. You'll receive care from experienced stroke specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all stroke clinical trials near you to find additional studies recruiting in your area.

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