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NCT07160114Completed

Task-oriented Training With Electrical Stimulation Glove on Hand Function and Dexterity in Chronic Stroke Patients

Source: ClinicalTrials.gov · Last updated 8 Sept 2025

Brief summary (registry, in English)

Stroke often causes long-lasting weakness and difficulty using the hands, which limits independence in daily life. Many patients find it hard to perform everyday tasks such as dressing, eating, or writing. Rehabilitation usually includes task-oriented training (TOT), which means practicing meaningful activities that mimic real-life situations. This study is testing whether adding a new device called an electrical stimulation glove (ESG) can make hand training more effective for people living with chronic stroke. The glove delivers gentle electrical impulses to the muscles in the hand while patients practice functional tasks. This stimulation may help activate weak muscles and improve coordination during rehabilitation. Participants in this study are divided into two groups: One group receives task-oriented training with the electrical stimulation glove, The other group receives task-oriented training only. Therapy includes warm-up exercises, task practice such as pegboard activities, grasping and releasing objects, and everyday skills, followed by cool-down exercises. The study is being carried out at CMH Multan, Pakistan, and involves adult men and women between 40 and 60 years of age who have experienced a stroke more than six months earlier. Outcomes are measured with standard rehabilitation tools that assess hand function, motor recovery, and dexterity. This research may help determine whether the electrical stimulation glove can be used alongside routine rehabilitation programs to support better recovery of hand function in people with stroke.

Status (registry)
Completed
Study type
Interventional
Enrollment
40 (actual)
First submitted
30 Aug 2025
Start date
15 Apr 2025
Primary completion date
19 Aug 2025
Lead sponsor
University of Lahore
Diseases
Stroke
NCT number
NCT07160114

What you commit to

  • Study type: Interventional
  • Participants enrolled: 40
  • From 15 Apr 2025 to the primary completion date, 19 Aug 2025
  • 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

  • Pre-existing arm impairment such as rheumatoid arthritis
  • Cardiac pacemaker
  • Recurrent or progressive stroke
  • History of seizure within 2 years (Anderson \& White, 2023)

Other

  • Patients with other neurological impairments
  • Unconscious patients due to any other cause

Who the study is looking for

  • Patients after the six months of first stroke event (chronic stroke patient)
  • Mini mental scale grade (24/above)
  • Medically and neurologically stable condition
  • No visual or auditory defects (Anderson \& White, 2023)

Age in the registry: 40 years to 60 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 University of Lahore Teaching Hospital
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

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