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NCT04813120Completed

Digital Mirror Therapy With Uni- and Bilateral Mirror Visual Feedback After Stroke: Treatment Effects and EEG Evidence

The Use of a New Digital Mirror Therapy System Providing Unilateral and Bilateral Mirror Visual Feedback for Patients With Stroke: Treatment Effects and EEG-physiological Evidence

Source: ClinicalTrials.gov · Last updated 21 Aug 2024

Brief summary (registry, in English)

The specific study aims will be: 1. To examine the treatment effects of a new digital mirror therapy (MT) system versus a mirror box in patients with stroke by conducting a 4-group randomized controlled trial. 2. To examine the electrophysiological mechanisms of uni-mirror visual feedback (uni-MVF) condition with unimanual training mode, uni-MVF condition with bimanual training mode, and bi-MVF condition with bimanual training mode in the new MT system by EEG.

Status (registry)
Completed
Study type
Interventional
Enrollment
47 (actual)
First submitted
21 Mar 2021
Start date
1 Aug 2021
Primary completion date
31 Jul 2024
Lead sponsor
Chang Gung Memorial Hospital
Diseases
Stroke
NCT number
NCT04813120

What you commit to

  • Study type: Interventional
  • Participants enrolled: 47
  • From 1 Aug 2021 to the primary completion date, 31 Jul 2024
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • other major medical diseases or comorbidities that have influenced upper-limb usage or caused severe pain
    • Part II: Investigation of the Electrophysiological Mechanisms Underlying Different MVF Conditions by EEG
  • other major medical diseases or comorbidities, such as neurological and psychiatric diseases, that have caused severe pain of upper-limb or interfered brain neural activities

Other

  • global or receptive aphasia;
  • severe neglect measured by line bisection test;
  • global or receptive aphasia;
  • severe neglect measured by line bisection test;

Who the study is looking for

  • diagnosed with a unilateral stroke;
  • at least 6 months after stroke onset;
  • age between 20 and 80 years old;
  • having a baseline score of Fugl-Meyer Assessment (FMA) in a range of 20 to 60;
  • able to follow the study instructions;
  • capable of participating in therapy and assessment sessions
  • diagnosed with a unilateral stroke;
  • at least 2 weeks after stroke onset and medical stable;
  • aged 20 to 80 years;
  • having a baseline score of FMA ≥ 40 and wrist flexion ≥ 20 degrees in order to perform EEG motor tasks;
  • both wrist flexion and extension scores of Modified Ashworth Scale ≤ 1;
  • able to follow the study instructions

Criteria the registry did not label

  • Part Ⅰ: Validation of Treatment Efficacy of the New Digital MT System with Different MVF Conditions and Training Modes

Age in the registry: 20 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Taoyuan Chang Gung Memorial Hospital
Coordinator of this site? Confirm its status
Taoyuan CityTaiwanUnknown status
Lo-Sheng Sanatorium and Hospital
Coordinator of this site? Confirm its status
Taoyuan CityTaiwanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.