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Effct of Rehabilitation in Stroke Recovery

Not Applicable
Conditions
stroke.
stroke, not specified as haemorrhage or infarction
Registration Number
IRCT2016102430477N1
Lead Sponsor
Vice Chancellor of Research, Shiraz University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

First-ever stroke resulting in right or left upper limb paresis and stroke had occurred between 2 weeks and 3 months; CT or MRI documenting a monohemispheric lesion as determined by a neurologist; Age between 18 and 80 years old; Patients with right-hand dominant according to Edingburg handedness scale; Patients with severe motor deficit of wrist extensor (score of 2 or less in strength test scale); Patients with severe to moderate motor impairment of affected upper limb (points less than 45 in items related to upper limb motor function); Not taking anti-spasticity drugs.
Exclusion criteria:
Other neurological diseases; Presence of pain, fracture, surgical history and joint dislocation of upper extremity; Contraindications to transcranial magnetic stimulation (TMS) including cardiac pacemaker, metal implants in skulls or eye, past history of seizure ; Presence of dementia, severe cognitive impairment (score of less than 24 points on the mini-mental status examination), aphasia and depression that made the patient uncooperative; Current use of drugs that could affect the excitability of the motor cortex, such as anti-epileptic and psychoactive drugs.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rest motor threshold. Timepoint: before intervention, after intervention. Method of measurement: TMS device.;Active motor threshold. Timepoint: before intervention, after intervention. Method of measurement: TMS device.;Recruitment curve. Timepoint: before intervention, after intervention. Method of measurement: TMS device.;Cortical silent period. Timepoint: before intervention, after intervention. Method of measurement: TMS device.;Ipsilateral silent period. Timepoint: before intervention, after intervention. Method of measurement: TMS device.
Secondary Outcome Measures
NameTimeMethod
Measuring performance in activities of daily living. Timepoint: before intervention, after intervention. Method of measurement: Modified Barthel Index.;Spasticity. Timepoint: before intervention, after intervention. Method of measurement: modified modified ashworth scale.;Wrist extensor muscle strength. Timepoint: before intervention, after intervention. Method of measurement: isokinetic dynamometer biodex device.;Assessment of motor function. Timepoint: before intervention, after intervention. Method of measurement: Fugl-Meyer Assessment.
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