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Robotic Therapy and Brain Stimulation in the Early Phase After Stroke

Not Applicable
Active, not recruiting
Conditions
Stroke
Interventions
Device: Robotic Therapy
Device: Sham stimulation
Device: Active stimulation
Registration Number
NCT03230695
Lead Sponsor
University of Sao Paulo General Hospital
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.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
24
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

Pregnancy

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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Sham stimulation + robotic therapySham stimulationSham transcranial direct current stimulation will be applied during 20 minutes prior to robotic training. Number of interventions sessions: 1
Active stimulation + robotic therapyRobotic TherapyActive transcranial direct current stimulation will be applied during 20 minutes prior to robotic training. Number of interventions sessions: 1
Sham stimulation + robotic therapyRobotic TherapySham transcranial direct current stimulation will be applied during 20 minutes prior to robotic training. Number of interventions sessions: 1
Active stimulation + robotic therapyActive stimulationActive transcranial direct current stimulation will be applied during 20 minutes prior to robotic training. Number of interventions sessions: 1
Primary Outcome Measures
NameTimeMethod
Movement SmoothnessKinematic assessment at baseline, immediately after intervention; and 24h after.

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

Secondary Outcome Measures
NameTimeMethod
Number of peaks of the movementkinematic assessment at baseline, immediately after intervention; and 24h after.

Number of peaks of the movement is calculated as the negative of the number of peaks in the speed profile.

Jerk metric of the movementkinematic assessment at baseline, immediately after intervention; and 24h after

Jerk metric of the movement is calculated by dividing the negative mean jerk magnitude by the peak speed.

Trial Locations

Locations (1)

Suzana Bleckmann Reis

🇧🇷

São Paulo, Brazil

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