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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
The Hong Kong Polytechnic University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Mirror therapy, Stroke, Hand function, Cost-effectiveness

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    December 3, 2020
    Last Updated
    February 10, 2021
    Sponsor
    The Hong Kong Polytechnic University
    Collaborators
    University of Canterbury, National University of Singapore
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    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

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