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NCT07710937Active, not recruiting

Visual and Auditory Electromyography Biofeedback Among Stroke Patients

Comparative Effects of Visual and Auditory Electromyography Biofeedback Combined With Conventional Physiotherapy on Balance, Functional Mobility, Motor Function, and Functional Independence Among Patients With Stroke: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 14 Oct 2026

Brief summary (registry, in English)

Stroke commonly results in impairments of balance, mobility, and lower extremity motor function that limit independence in daily activities. Electromyography (EMG) biofeedback enhances motor relearning by providing real-time feedback regarding muscle activation. Although both visual and auditory EMG biofeedback have demonstrated benefits in stroke rehabilitation, evidence directly comparing these feedback modalities remains limited. This randomized controlled trial aims to compare the effects of visual and auditory EMG biofeedback, each combined with conventional physiotherapy, on balance, functional mobility, motor function, and functional independence in individuals with stroke.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
84 (estimated)
First submitted
14 Jul 2026
Start date
9 Apr 2026
Primary completion date
10 Sept 2026
Lead sponsor
University of Lahore
Diseases
Stroke
NCT number
NCT07710937

What you commit to

  • Study type: Interventional
  • Planned participants: 84
  • From 9 Apr 2026 to the primary completion date, 10 Sept 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.

Other illness

  • Severe systemic disease that could interfere with participation
  • Peripheral vascular disease affecting the lower extremities

Other

  • Traumatic injury or lesion affecting the lower extremities
  • Lower-limb amputation
  • Fixed ankle contracture
  • Motion sickness or intolerance to rehabilitation technology

Who the study is looking for

  • Age between 20 and 30 years
  • Male or female participants
  • Clinically diagnosed hemiplegic stroke.
  • Medically stable and able to participate in rehabilitation.
  • No visual impairment that would interfere with visual biofeedback.
  • No hearing impairment that would interfere with auditory biofeedback.
  • No sensory aphasia affecting the ability to understand study instructions.

Age in the registry: 40 years to 65 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
Nishtar Hospital Multan
Coordinator of this site? Confirm its status
Multan KhurdPakistanUnknown status

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