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Clinical Trials/NCT03230695
NCT03230695
Active, not recruiting
Not Applicable

Effects of Robotic Therapy and Transcranial Direct Current Stimulation on Motor Performance of the Paretic Upper Limb in the Early Phase After Stroke

University of Sao Paulo General Hospital1 site in 1 country24 target enrollmentAugust 3, 2017
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
University of Sao Paulo General Hospital
Enrollment
24
Locations
1
Primary Endpoint
Movement Smoothness
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

Stroke is the second cause of death worldwide and the majority of the survivors remain with motor impairments. Inhibition of the motor cortex of the unaffected hemisphere has emerged as a potential intervention to enhance effects of other rehabilitation strategies on improvement of motor performance of the paretic upper limb. In this proof-of-concept study we will evaluate the effects of inhibition of the motor cortex of the unaffected hemisphere associated with robotic therapy on improvement of motor performance of the paretic upper limb in the early phase post-stroke.

Detailed Description

The main goal of this study is to test the proof of concept of benefits of inhibition of the motor cortex of the unaffected hemisphere on learning evaluated by improvement in kinematics of motor performance, in patients with upper limb paresis in the early phase post-stroke. For this purpose, patients will be randomized to receive real or sham transcranial direct current stimulation before a session of robotic therapy. Data will be collected by kinematic assessment performed automatically by the robot at baseline, immediately after and 24h after the intervention. The working hypothesis is that one session of upper limb motor training will lead to improvement of performance in metrics of kinematics, and this improvement will be maintained up to 24h after the end of the training.

Registry
clinicaltrials.gov
Start Date
August 3, 2017
End Date
July 2025
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Ischemic or hemorrhagic stroke onset from 3 days to 9 weeks before, confirmed by computed tomography or magnetic resonance imaging.
  • Motor impairment of an upper limb, defined as a score between 1 - 3 in the Medical Research Council Scale, for at lest one the following movements: elbow extension, shoulder flexion, or shoulder extension.
  • Ability to provide written informed consent.
  • Ability to comply with the schedule of interventions and evaluations in the protocol.

Exclusion Criteria

  • Severe spasticity at the paretic elbow, wrist or fingers, defined as a score of \> 3 in the Modified Ashworth Spasticity Scale.
  • No active shoulder and elbow movements
  • Uncontrolled medical problems such as end-stage cancer or renal disease
  • Potential contraindications to transcranial direct current stimulation: history of seizures, lesions on the scalp, intracranial metal implants, prior intracranial surgery, use of drugs that interfere on cortical excitability (such as antiepileptic drugs, benzodiazepines)
  • Other neurological disorders such as Parkinson's disease
  • Psychiatric illness
  • Aphasia or severe cognitive deficits that compromise comprehension of the experimental protocol or ability to provide consent.
  • Hemineglect
  • Cerebellar lesions or on cerebellar pathways
  • Contact precautions

Outcomes

Primary Outcomes

Movement Smoothness

Time Frame: Kinematic assessment at baseline, immediately after intervention; and 24h after.

The speed shape, calculated as mean speed divided by peak speed.

Secondary Outcomes

  • Number of peaks of the movement(kinematic assessment at baseline, immediately after intervention; and 24h after.)
  • Jerk metric of the movement(kinematic assessment at baseline, immediately after intervention; and 24h after)

Study Sites (1)

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