Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06998485

Substrates for Post-Stroke Arm Rehabilitation

Led by Massachusetts General Hospital · Updated on 2026-03-11

50

Participants Needed

1

Research Sites

238 weeks

Total Duration

On this page

Sponsors

M

Massachusetts General Hospital

Lead Sponsor

N

National Institute of Neurological Disorders and Stroke (NINDS)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Difficulty moving the arm is very common and a major cause of disability after stroke. Although rehabilitation therapies (i.e., occupational and physical therapy) are the most common treatments used to improve arm motor function, it remains unknown how therapy actually changes brain pathways after stroke. This project seeks to generate fundamental knowledge about brain pathways that allow people to move their arm after stroke and how these pathways change with rehabilitation; we expect this knowledge to translate to new therapies to reduce stroke-related disability. We plan to enroll N = 50 patients with moderate to severe difficulty moving their arm after ischemic or hemorrhage stroke during the subacute period (3 to 6 months post stroke) into either 30 hours over 6 weeks of Arm Basis Training (a protocolized form of occupational therapy targeting motor control) or usual care. We will perform kinematic motor assessments, neuroimaging, and neurophysiology before and after therapy in order to test the hypothesis that intensive, target training improves arm motor control and induces corresponding anatomical and physiological changes of associated brain pathways.

CONDITIONS

Official Title

Substrates for Post-Stroke Arm Rehabilitation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • First time unilateral ischemic or hemorrhagic stroke occurring within 3 to 6 months
  • Upper extremity motor impairment with Upper Extremity Fugl-Meyer Assessment (UE-FMA) score of 44 or less
  • Ability to participate in a 6-week intensive upper extremity intervention in English as determined by a licensed occupational therapist
Not Eligible

You will not qualify if you...

  • Bilateral stroke
  • Unstable medical condition affecting functional status
  • Pre-stroke upper extremity injury or condition limiting use
  • Visual or auditory impairment limiting ability to participate
  • Significant aphasia (NIHSS sub-item 9 > 1) or cognitive deficits (NIHSS 1a, 1b, or 1c > 1)
  • Known or expected inability to maintain follow-up through study and post-assessment
  • Contraindications to MRI or transcranial magnetic stimulation (TMS)
  • Known history of uncontrolled seizure disorder

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Laboratory for Translational Neurorecovery, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital

Boston, Massachusetts, United States, 02114

Actively Recruiting

Loading map...

Research Team

C

Caroline Lambert, BA

CONTACT

J

Julie DiCarlo, MS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here