Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT02369770

Sensory-Motor Rehabilitation Post Stroke

Led by University of Maryland, Baltimore · Updated on 2026-04-21

140

Participants Needed

1

Research Sites

453 weeks

Total Duration

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AI-Summary

What this Trial Is About

Early after stroke, patients often have significant motor impairment and sensory deficit. Evidence has demonstrated heightened plasticity and significant recovery in the acute phase (first months) post stroke but there has been a lack of effective and practical protocols and devices for early intensive sensorimotor therapy.This research study will conduct a randomized clinical trial of an intensive motor-sensory rehabilitation on patients with acute stroke using a wearable rehabilitation robot. The primary aims are to facilitate sensorimotor recovery, reduce ankle impairments, and improve balance and gait functions. This clinical trial will be conducted on the Study and Control groups of acute stroke survivors.

CONDITIONS

Official Title

Sensory-Motor Rehabilitation Post Stroke

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • First time unilateral acute stroke, hemorrhagic or ischemic, from 24 hours after hospital admission up to 1 year post stroke
  • Hemiplegia or hemiparesis
  • Age between 18 and 80 years
  • Presence of ankle impairments
Not Eligible

You will not qualify if you...

  • No or very mild ankle impairment
  • Unstable medical conditions that interfere with training and exercise
  • Severe cardiovascular disorders preventing moderate movement exercises
  • Cognitive impairment or aphasia preventing understanding or following instructions
  • Pressure ulcers, recent surgical incisions, or active skin disease with open wounds below the treated knee
  • Severe leg pain

AI-Screening

AI-Powered Screening

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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

R

Raziyeh Baghi, Ph.D.

CONTACT

T

Thanh Phan, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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