Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
NCT02359253

Robot Aided Rehabilitation - Intervention

Led by University of Maryland, Baltimore · Updated on 2025-07-09

72

Participants Needed

1

Research Sites

428 weeks

Total Duration

On this page

Sponsors

U

University of Maryland, Baltimore

Lead Sponsor

N

National Institute on Disability, Independent Living, and Rehabilitation Research

Collaborating Sponsor

AI-Summary

What this Trial Is About

Sensorimotor impairments following stroke often involve complex pathological changes across multiple joints and multiple degrees of freedom of the arm and hand, thereby rendering them difficult to diagnose and treat. The objective of this study is to evaluate multi-joint neuromechanical impairments in the arm and hand, then conduct impairment-specific treatment, and determine the effects of arm versus hand training and the effects of passive stretching before active movement training.

CONDITIONS

Official Title

Robot Aided Rehabilitation - Intervention

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • First focal unilateral stroke lesion, ischemic or hemorrhagic
  • Stroke occurred 1 to 12 months before enrollment
  • Rated between stages 2 and 4 on the Chedoke McMaster Stroke Assessment for arm and hand recovery
Not Eligible

You will not qualify if you...

  • Presence of apraxia
  • Mini Mental Status Exam score less than 22
  • Severe shoulder pain rated 7 or higher out of 10
  • Severe contracture in the upper extremity
  • Unable to sit in a chair for 3 hours continuously
  • Musculoskeletal injuries unrelated to stroke
  • Poor fit in study equipment
  • Botox injections in upper extremity within past 4 months
  • Participation in other gait or upper extremity intervention studies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Maryland, Baltimore

Baltimore, Maryland, United States, 21201

Actively Recruiting

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Research Team

S

Soh-Hyun Hur

CONTACT

K

Kyung Koh, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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