Enhanced Mirror Therapy for Improving Brain Reorganization and Function in Stroke
Primary Purpose
Stroke
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Enhanced mirror therapy
Standard mirror therapy
Sponsored by

About this trial
This is an interventional treatment trial for Stroke focused on measuring Mirror therapy, Stroke, Hand function, Cost-effectiveness
Eligibility Criteria
Inclusion Criteria:
- adults with stroke (40-75 years old), with normal or corrected-to-normal vision and hearing;
- post-stroke duration of ≥ 6 months, before the start of data collection;
- no severe deficits in memory, communication, or the ability to understand verbal instructions.
Exclusion Criteria:
- participants with recurrent stroke; and
- those who score < 24 on the Mini-Mental State Examination (MMSE).
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Enhanced mirror therapy group
Standard mirror therapy group
Arm Description
Participants in this group will perform complex and randomized finger opposition and reposition movements based on the training protocol, along with enhanced complexity and altered clarity of the displayed image.
Participants in this group will perform simple and sequential finger opposition and reposition movements, along with a clear image showing the exercising hand of the participants.
Outcomes
Primary Outcome Measures
Blood oxygenated haemoglobin concentrations
Functional near-infrared spectroscopy (fNIRS) will be used to assess neurovascular changes (blood oxygenated haemoglobin concentrations) in the M1. Higher the score obtained indicate better facilitation of the primary motor cortex.
Secondary Outcome Measures
Wrist and hand function
The Fugl-Meyer assessment (wrist and hand subcomponents) for the assessment of the upper limb function. The scale has a maximum score of 66 and a minimum of 34 with higher the score obtained better the wrist and hand function.
Upper limb function
The Action Research Arm Test (ARAT), to assess upper-limb function. The ARAT scores range from 0-57, with a maximum score of 57 points indicating better performance of the upper limb.
Economic evaluation
The Euro quality of life (EuroQol, 5 dimensions and 5 levels 62) survey, will assess the quality-adjusted life years (QALY) for the cost-effectiveness estimation. The EQ-5D-5L response will be converted into utility scores, which will be used to estimate gains or losses in quality-adjusted life-years (QALYs) over the follow-up period. The higher the score obtained better the quality-life-adjusted-years due to the intervention.
Full Information
NCT ID
NCT04749199
First Posted
December 3, 2020
Last Updated
February 10, 2021
Sponsor
The Hong Kong Polytechnic University
Collaborators
University of Canterbury, National University of Singapore
1. Study Identification
Unique Protocol Identification Number
NCT04749199
Brief Title
Enhanced Mirror Therapy for Improving Brain Reorganization and Function in Stroke
Official Title
Enhanced Mirror Therapy for Improving Brain Reorganization and Function in Stroke: A Pilot Randomized Controlled Trial With Economic Evaluation
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
May 1, 2021 (Anticipated)
Primary Completion Date
December 1, 2021 (Anticipated)
Study Completion Date
November 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hong Kong Polytechnic University
Collaborators
University of Canterbury, National University of Singapore
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This research aims to test the methodological procedures and obtain preliminary results regarding the therapeutic and cost-effectiveness of enhanced mirror therapy relative to standard mirror therapy for improving brain reorganization and upper limb function in individuals with stroke.
Detailed Description
Stroke is among the leading causes of mortality and disability, worldwide. Muscle weakness and other complications associated with stroke can result in decreased quality of life and significant declines in the activities of daily living. Mirror therapy has been shown to have a moderate effect, facilitating the functional recovery among individuals who have experienced a stroke. A prototype for a computerized, mirror therapy device was developed and found to be feasible. Recently, the investigators published a critical review and an activation likelihood estimation (ALE) meta-analysis analysing the widespread reports of brain activity associated with mirror therapy. Observations using functional near-infrared spectroscopy (fNIRS) to evaluate a group of people with stroke (n = 14) and healthy volunteers (n = 18) revealed that performing complex tasks during the mirror therapy paradigm enhanced top-down motor facilitation in the ipsilesional/ipsilateral hemisphere relative to the moving limb. An important next step in this series of studies is to evaluate the training effects associated with the performance of complex tasks during mirror therapy among stroke patients, using the designed computerized mirror therapy device to deliver the enhanced mirror therapy training. The results of this study will help the investigators to understand the underlying mechanisms through which mirror therapy facilitates motor rehabilitation and will add to the body of literature describing the best, evidence-based practices for mirror therapy during stroke rehabilitation. The investigators propose a pilot study (n = 30) to test the methodological procedures and obtain preliminary results for a fully powered, randomized, controlled trial (RCT), combined with economic evaluation, to compare the therapeutic and cost-effectiveness between standard mirror therapy and enhanced (complex task and blurred image) mirror therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Mirror therapy, Stroke, Hand function, Cost-effectiveness
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A blinded assessor and statistician will evaluate a two-arm, parallel-group, RCT that compares enhanced mirror therapy, comprised of increased task complexity and mirror image blurriness, with standard mirror therapy training among 30 participants with chronic stroke.
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Enhanced mirror therapy group
Arm Type
Experimental
Arm Description
Participants in this group will perform complex and randomized finger opposition and reposition movements based on the training protocol, along with enhanced complexity and altered clarity of the displayed image.
Arm Title
Standard mirror therapy group
Arm Type
Sham Comparator
Arm Description
Participants in this group will perform simple and sequential finger opposition and reposition movements, along with a clear image showing the exercising hand of the participants.
Intervention Type
Behavioral
Intervention Name(s)
Enhanced mirror therapy
Other Intervention Name(s)
Complex task mirror therapy
Intervention Description
Participants of the enhanced mirror therapy group will perform complex, randomized, finger opposition and reposition movements, using the thumb, index, middle, ring, and little fingers, and will be shown a 35% blurred visual feedback through the computerized mirror therapy device. Each participant will receive a mirror training session for 60 minutes each day, three times per week for four consecutive weeks.
Intervention Type
Behavioral
Intervention Name(s)
Standard mirror therapy
Other Intervention Name(s)
Simple task mirror therapy
Intervention Description
Participants allocated to this group will perform simple, sequential finger opposition and reposition movements, using the thumb, index, middle, ring, and little fingers, and will be shown a clear image of the exercising hand. Each participant will receive a mirror training session for 60 minutes each day, three times per week for four consecutive weeks.
Primary Outcome Measure Information:
Title
Blood oxygenated haemoglobin concentrations
Description
Functional near-infrared spectroscopy (fNIRS) will be used to assess neurovascular changes (blood oxygenated haemoglobin concentrations) in the M1. Higher the score obtained indicate better facilitation of the primary motor cortex.
Time Frame
Change in score at the end of 4-weeks of intervention (T1), and six months post-intervention (T2)
Secondary Outcome Measure Information:
Title
Wrist and hand function
Description
The Fugl-Meyer assessment (wrist and hand subcomponents) for the assessment of the upper limb function. The scale has a maximum score of 66 and a minimum of 34 with higher the score obtained better the wrist and hand function.
Time Frame
Change in score at the end of 4-weeks of intervention (T1), and six months post-intervention (T2)
Title
Upper limb function
Description
The Action Research Arm Test (ARAT), to assess upper-limb function. The ARAT scores range from 0-57, with a maximum score of 57 points indicating better performance of the upper limb.
Time Frame
Change in score at the end of 4-weeks of intervention (T1), and six months post-intervention (T2)
Title
Economic evaluation
Description
The Euro quality of life (EuroQol, 5 dimensions and 5 levels 62) survey, will assess the quality-adjusted life years (QALY) for the cost-effectiveness estimation. The EQ-5D-5L response will be converted into utility scores, which will be used to estimate gains or losses in quality-adjusted life-years (QALYs) over the follow-up period. The higher the score obtained better the quality-life-adjusted-years due to the intervention.
Time Frame
Change in score at the end of 4-weeks of intervention (T1), and six months post-intervention (T2)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
adults with stroke (40-75 years old), with normal or corrected-to-normal vision and hearing;
post-stroke duration of ≥ 6 months, before the start of data collection;
no severe deficits in memory, communication, or the ability to understand verbal instructions.
Exclusion Criteria:
participants with recurrent stroke; and
those who score < 24 on the Mini-Mental State Examination (MMSE).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stanley John Winser
Phone
27666746
Email
stanley.j.winser@polyu.edu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stanley John Winser
Organizational Affiliation
Hong Kong Polytechnic University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Enhanced Mirror Therapy for Improving Brain Reorganization and Function in Stroke
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