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NCT03622879Completed

Mirror Therapy With Cutaneous Electrical Sensory Stimulation on Lower Limb Motor Functions in Stroke

Effect of Mirror Therapy With Cutaneous Electrical Sensory Stimulation on Lower Limb Motor Functions in People With Stroke: A Single-blinded Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

This study aims to evaluate the effectiveness of concurrent mirror therapy (MT) and transcutaneous electrical nerve stimulation (TENS) in augmenting the efficacy of the lower limb task-oriented training in people with stroke. It is hypothesize that MT combined with TENS would be superior to sham-mirror therapy with TENS, or MT with placebo-TENS, or control training only in improving lower limb motor functions and walking ability in people with stroke when combined with the lower limb task-oriented training.

Status (registry)
Completed
Study type
Interventional
Enrollment
100 (actual)
First submitted
10 Jul 2018
Start date
2 Jul 2018
Primary completion date
1 Jun 2026
Lead sponsor
The Hong Kong Polytechnic University
Diseases
Stroke
NCT number
NCT03622879

What you commit to

  • Study type: Interventional
  • Participants enrolled: 100
  • From 2 Jul 2018 to the primary completion date, 1 Jun 2026
  • 1 site 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.

Prior treatment

  • are involved in drug studies or other clinical trials.

Other illness

  • have any additional medical, cardiovascular or orthopaedic condition that would hinder proper treatment or assessment;

Other

  • have visual deficits that may hinder them from benefiting from the mirror visual feedback;
  • have receptive dysphasia; or

Who the study is looking for

  • have had a single stroke with ischemic brain injury or intracerebral haemorrhage diagnosed by magnetic resonance imaging or computed tomography within the previous 6 to 36 months;
  • have at least 5 degrees of active ankle dorsiflexion in the antigravity position;
  • are able to walk 10 m independently with or without a walking aid;
  • are able to score 6 or higher out of 10 on the abbreviated mental test;
  • have no unilateral neglect, hemianopia or apraxia;
  • have no skin allergy (e.g. redness or itchiness to the electrical stimulation pads) to electrical stimulation or electrodes; and
  • are able to follow instructions and give informed consent.

Age in the registry: 55 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
The Hong Kong Polytechnic University
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaUnknown status

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