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NCT07282938Recruiting

Combined Effects of Soft Robotic Hand and Electrical Stimulation on Hand Function in Stroke Survivors

Source: ClinicalTrials.gov · Last updated 18 Jun 2026

Brief summary (registry, in English)

Stroke is a clinically delineated syndrome, which is characterised by an acute, focal neurological deficit resulting from vascular injury (infarction or haemorrhage) within the central nervous system. Notably, around 80 percent of stroke survivors experience post-stroke deficits in upper extremity (UE) motor performance, impacting grip strength, dexterity, and functional independence, which greatly hinder the ability of stroke patients to carry out activities of daily living (ADL), and in turn affects their overall quality of life (QOL).One potential solution to these difficulties is the creation of rehabilitation robotic devices that incorporate hand technology and electrical stimulation. Although soft robotic assistive devices and electrical stimulation have each shown positive effects on motor recovery, their combined use has yet to be thoroughly investigated. This study intends to determine if the simultaneous application of these therapies can speed up rehabilitation results in comparison to independent therapies. Stroke Participants will be divided into two groups, Experimental group and Control group. Both the groups will receive intervention for 40 min/day, 03 days/week, for 08 week and measurements will be taken prior to the treatment, after 4 weeks of treatment and 8 weeks post-treatment.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
64 (estimated)
First submitted
2 Dec 2025
Start date
8 Dec 2025
Primary completion date
30 Jun 2026
Lead sponsor
Lahore University of Biological and Applied Sciences
Diseases
Stroke
NCT number
NCT07282938

What you commit to

  • Study type: Interventional
  • Planned participants: 64
  • From 8 Dec 2025 to the primary completion date, 30 Jun 2026
  • 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

  • Presence of other neurological, neuromuscular, orthopedic diseases, or
  • conditions that may interfere with task performance.

Other

  • Participants with sensory disturbances in the fingers

Who the study is looking for

  • Diagnosed with their first episode of stroke.
  • Participants with 3-6 months post stroke.
  • Participants with normal cognition on Montreal Cognitive Assessment (MOCA) ≥24.
  • Participants with the ability to extend Metacarpophalangeal (MCP) and Proximal Interphalangeal (PIP) joint to 180 degree passively
  • Modified Ashworth Scale \< 2.
  • Participants with the score of 10 to 16 on National Institute of Health Stroke Scale Score (NIHSS Score).

Age in the registry: 45 years to 65 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
Pakistan Society for the Rehabilitation of the Disabled (PSRD)
Coordinator of this site? Confirm its status
LahorePakistanRecruiting
Shadman Medical Center, Stroke Rehabilitation
Coordinator of this site? Confirm its status
LahorePakistanRecruiting

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