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Neurorehabilitation Using a Virtual Reality-based Mirror Therapy

Not Applicable
Completed
Conditions
Rehabilitation, Mirror Neurons, Stroke
Interventions
Other: task-oriented training
Registration Number
NCT03329417
Lead Sponsor
National Cheng-Kung University Hospital
Brief Summary

In the proposed study, the investigators assumed that mirror therapy combined with virtual reality technology will provide a better treatment effects than traditional mirror therapy for the patients with unilateral stroke. The aim of the study is to examine the difference in the treatment effects among the combination of task-oriented training with either virtual reality based mirror therapy, mirror therapy or traditional occupational therapy on the upper extremity function and brain activity of the stroke patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
134
Inclusion Criteria
  1. Clinical diagnosis of stroke with unilateral side involved;
  2. A score of Mini-mental state examination greater than 24 for proving higher mental function;
  3. Time of onset > 6 months before treatment begins, and
  4. Premorbid right-handedness.
Exclusion Criteria
  1. Vision loss;
  2. Major cognitive-perceptual deficit;
  3. Other brain disease.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Mirror therapy using a mirror boxtask-oriented trainingThe program includes 30 minutes of mirror therapy, followed by 20 minutes of regular motor task specific training in each treatment session.
Virtual reality based mirror therapytask-oriented trainingThe program includes 30 minutes treatment session of virtual reality mirror therapy, followed by 20 minutes of motor task specific training in each treatment session.
Traditional occupational therapytask-oriented trainingThe program includes 30 minutes of traditional occupational therapy (sensorimotor facilitation techniques, such as: Rood, Bobath and propriocetive-neuromuscular-facilitation), followed by 20 minutes of motor task specific training in each treatment session.
Primary Outcome Measures
NameTimeMethod
Change in the result of Fugl-Meyer assessment (FMA) for motor function of upper extremity testbaseline, 6 weeks and 18 weeks

Each item is rated on a three-point ordinal scale (2 points for the detail being performed completely, 1 point for the detail being performed partially, and 0 for the detail not being performed). The maximum motor performance score is 66 points for the upper extremity.

Change in the result of Box and blocks testbaseline, 6 weeks and 18 weeks

The score is the number of blocks carried from one box to the other in one minute. Higher values represent a better outcome.

Change in the result of Motor Activity Logbaseline, 6 weeks and 18 weeks

Semi-structured interview examine how much and how well the subject uses their more-affected arm for 30 ADLs. Score range from 0-180. Higher values represent a better outcome.

Change in the result of Modified Ashworth scale (MAS)baseline, 6 weeks and 18 weeks

Muscle tone is defined by the resistance of a muscle being stretched without resistance. The MAS scores were distributed across the entire scale, ranging from 0 to 4, that is convenient for the clinician use. The grading of the scale is described as below: 0) no increase in muscle tone; 1) minimal resistance at the end of the range of motion; 1+) slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the reminder (less than half) of the ROM; 2) more marked increase in tone but only after part is easily flexed; 3) considerable increase in tone; and 4) passive movement is difficult and affected part is rigid in flexion or extension.

Change in the result of Semmes-Weinstein monofilament (SWM) testbaseline, 6 weeks and 18 weeks

The Semmes-Weinstein monofilamenttest examines the cutaneous pressure threshold, range from 1.65-6.65. Higher values represent a worse outcome.

Secondary Outcome Measures
NameTimeMethod
Changes in Cortical Excitability Assessed by Transcranial Magnetic Stimulationbaseline and 6 weeks

Cortical silent period of to evaluate intercortical facilitation of brain. Lower values represent a better outcome.

Change in Power Spectrum of the Electroencephalography (EEG)baseline and 6 weeks

Power spectrum is computed for the alpha (8-13 Hz) and beta (14-24 Hz) frequency bands. Higher values represent a better outcome.

Trial Locations

Locations (1)

National Cheng-Kung University Hospital

🇨🇳

Tainan, Taiwan

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