Skip to main content
OpenTrials
Completed

NCT Number: NCT03854487

Effect of Mirror Therapy on Unilateral Neglect for Patients After Stroke

This is a single-blinded randomized controlled trial to investigate the effects of mirror therapy (MT), with reference to sham mirror (a glass wall) and control (a covered mirror), in reducing unilateral neglect for patients with stroke in 2 centres.

Completed

Looking for future studies?

Notify Me

Key information

About this study

Twenty-one subacute inpatients with left unilateral neglect after right-hemispheric stroke, recruited from 2 hospitals - Hong Kong and Guangzhou, in 1 and a half years, were randomly assigned to three groups; mirror therapy, sham therapy (in the form of a transparent glass wall), and control (covered mirror). The treatment programme for all groups consisted of 12 sessions (4 per week for 3 weeks) movement practice for the hemiplegic arm involved 5 table-top tasks graded according to the severity of patients' arm impairments. Blinded assessments were administered at baseline, 3-week postintervention, and 3-week follow-up upon completion of training.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ischemic or hemorrhagic stroke, confirmed by medical diagnoses compatible with a unilateral right lesion involvement (i.e. left hemiplegic), exhibited left visual field inattention or unilateral neglect by obtaining a total score of star cancellation subtest in the conventional battery of the Behavioural Inattention Test ≤ 51 (out of 54);
  • stroke with onset of neurological condition ≤ 6 months previously;
  • have normal or corrected-to-normal visual acuity better than 20/60 (6/18) in the better eye;
  • with hemiplegic upper extremity functional levels 3-7 as rated by Functional Test for the Hemiplegic Upper Extremity and is able to move against gravity;
  • ability to understand and follow simple verbal instructions, with Mini-mental State Examination ≥ 21;
  • ability to participate in a therapy session lasting at least 30 minutes;
  • consent to participant in the study

Exclusion criteria

  • prior neurological or psychiatric disorders;
  • severe spasticity (Modified Ashworth Scale >3) over paretic arm;
  • history of recent Botox injection or acupuncture to the paretic arm within the past three months;
  • participation in another clinical study elsewhere apart from the study site during recruitment

Treatment and study plan

Mirror Therapy

Behavioral

A mirror is placed at the midsagittal plane of the patient. The patients in the mirror therapy group watched the mirror illusion of the non-affected arm in the mirror and moved together with the affected arm. The treatment programme for all groups consisted of 12 sessions (4 per week for 3 weeks), each lasting for 30 minutes. The movement practice involved 5 table-top tasks and the patient was instructed to perform as many trials as possible in each session with a maximum of 30 trials per task, giving a total of 150 trials per session. Treatment activities are graded according to the severity of the patient's upper extremity impairment.

Sham mirror

Behavioral

A transparent glass wall is placed at the midsagittal plane of the patient. The patients in the sham mirror group watched the movements of the affected arm through the transparent glass wall and moved together with the non-affected arm. The treatment programme for all groups consisted of 12 sessions (4 per week for 3 weeks), each lasting for 30 minutes. The movement practice involved 5 table-top tasks and the patient was instructed to perform as many trials as possible in each session with a maximum of 30 trials per task, giving a total of 150 trials per session. Treatment activities are graded according to the severity of the patient's upper extremity impairment.

Covered mirror

Behavioral

A covered mirror is placed at the midsagittal plane of the patient. The patients in the control group watched the movements of the non-affected arm and moved together with the affected arm behind the covered mirror. The treatment programme for all groups consisted of 12 sessions (4 per week for 3 weeks), each lasting for 30 minutes. The movement practice involved 5 table-top tasks and the patient was instructed to perform as many trials as possible in each session with a maximum of 30 trials per task, giving a total of 150 trials per session. Treatment activities are graded according to the severity of the patient's upper extremity impairment.

Primary outcomes

  1. Unilateral neglect

    Time frame: Change of baseline to 3-week and to follow-up at 6-week

    Behavioural Inattention Test

  2. Allocentric and egocentric neglect

    Time frame: Change of baseline to 3-week and to follow-up at 6-week

    Gap Detection Test

  3. Functional performance related to unilateral neglect

    Time frame: Change of baseline to 3-week and to follow-up at 6-week

    Catherine Bergego Scale

Secondary outcomes

  1. Upper limb functions

    Time frame: Change of baseline to 3-week and to follow-up at 6-week

    Fugl-Meyer assessment

Sponsors and collaborators

Lead sponsor

The Hong Kong Polytechnic University

Other

Collaborators

  • Guangdong 999 Brain Hospital
  • Tung Wah Hospital

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2018
First posted
Feb 26, 2019
Registry last updated
Feb 26, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.