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NCT06739733Active, not recruiting

Effectiveness of Soft Robotic Glove Versus EMS on Hand Function and Quality of Life in Stroke Survivors (RCT)

Effectiveness of Soft Robotic Glove Versus EMS on Hand Function and Quality of Life in Stroke Survivors. A Randomized Clinical Trial

Source: ClinicalTrials.gov · Last updated 18 Dec 2024

Brief summary (registry, in English)

This study will evaluate the effectiveness of soft robotic gloves versus electrical muscle stimulation (EMS) in improving hand function and quality of life in stroke survivors. Stroke often leads to impaired hand mobility, impacting daily activities and reducing overall quality of life. Soft robotic gloves, designed to assist with hand movement, will provide mechanical support and encourage voluntary muscle activity. EMS, on the other hand, will stimulate muscle contraction through electrical impulses, potentially enhancing muscle strength and coordination.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
36 (actual)
First submitted
13 Dec 2024
Start date
1 Mar 2024
Primary completion date
1 Oct 2024
Lead sponsor
Superior University
Diseases
Stroke
NCT number
NCT06739733

What you commit to

  • Study type: Interventional
  • Participants enrolled: 36
  • From 1 Mar 2024 to the primary completion date, 1 Oct 2024
  • 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

  • Participants with severe vision or hearing impairment.
  • Neurological disorders including epilepsy, Alzheimer's disease, vertigo, Parkinson disease, and , muscular disorders which limit functional activity (OA, RA, etc).
  • Peripheral vestibular disorder.
  • Medications that affect balance, severe cardiovascular conditions, recent lower limb injury or surgery.
  • Contraindications for EMS: Patients with certain medical conditions, such as pacemakers, implantable cardioverter-defibrillators, or metal fragments in their body, that contraindicated the use of EMS were excluded.

Who the study is looking for

  • Had ischemic or hemorrhagic stroke ≤6 months.
  • Mini-mental status exam scores \> 24(7).
  • GCS score 11 to 15(2)
  • FMA-UE score \< 21(3)

Age in the registry: 50 years to 70 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
Ahmad block garden town canal road
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

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