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NCT06927284Recruiting

Effects Of Neurocognitive Therapy With And Without Soft Robotic Hand On Hand Function

Effects of Neurocognitive Therapy With and Without Soft Robotic Hand on Hand Function in Sub-acute Stroke

Source: ClinicalTrials.gov · Last updated 22 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

To determine the effect of neurocognitive therapy with and without a soft robotic hand on manual ability, dexterity, strength, spasticity and upper limb function in sub-acute stroke.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
46 (estimated)
First submitted
7 Apr 2025
Start date
10 Apr 2025
Primary completion date
30 Oct 2025
Lead sponsor
Riphah International University
Diseases
Stroke
NCT number
NCT06927284

What you commit to

  • Study type: Interventional
  • Planned participants: 46
  • From 10 Apr 2025 to the primary completion date, 30 Oct 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.

Prior treatment

  • Participants who have active pacemakers and other active implants.

Other illness

  • Participants who have a history of significant neurological or orthopedic disorders, other than stroke, that could interfere with upper limb motor or sensory recovery.

Other

  • Participants who have altered state of consciousness, severe aphasia, severe cognitive deficit.
  • Participants who have severe pathologies of traumatic and or rheumatic nature, severe pain in effected arm (\>5 on visual analog scale for pain) .

Who the study is looking for

  • Participants of Post stroke patients (6-12 weeks )
  • Participants with Spasticity \< 2 on modified Ashworth scale.
  • Participants with first ever stroke.
  • Participants with normal cognition \> 24 on MoCA
  • Participants must be able to provide informed consent
  • Hemiparesis with arm motor deficit as assessed by with NIHSS \>1(14)

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
Sheikh Zayad Hospital
Coordinator of this site? Confirm its status
LahorePakistanRecruiting

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