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NCT07080099Completed

Effects of Bimanual Intensive Therapy With Sensory Training in Post Stroke Patients

Effects of Bimanual Intensive Therapy With Sensory Training on Motor Function, Sensory Function and Functional Independence in Post Stroke Patients

Source: ClinicalTrials.gov · Last updated 23 Jul 2025

Brief summary (registry, in English)

Stroke is the major serious health burden and the leading cause of serious long term disability around the world. One of the most cumbersome deficits after a stroke is impairment in the contralateral upper limb. Bimanual intensive therapy (BIT) is a specialized approach used in rehabilitation for individuals, typically children, who have hemiplegia or hemiparesis, which means weakness or paralysis on one side of the body A therapy strategy known as "sensory training" aims to improve sensory integration and processing in people who struggle with sensory processing issues. The aim of this study is to determine the combined effects of bimanual intensive therapy with sensory training in addition conventional therapy on motor functions, sensory function and functional independence stroke patients.

Status (registry)
Completed
Study type
Interventional
Enrollment
38 (actual)
First submitted
14 Jul 2025
Start date
25 Feb 2024
Primary completion date
30 Sept 2024
Lead sponsor
Riphah International University
Diseases
Stroke
NCT number
NCT07080099

What you commit to

  • Study type: Interventional
  • Participants enrolled: 38
  • From 25 Feb 2024 to the primary completion date, 30 Sept 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

  • Patients with history of epilepsy
  • Patients with an history of an intracranial implant
  • Any other neurological conditions

Other

  • Patients with severe cardiopulmonary complications
  • Patients with the presence of a pacemaker
  • Patients with presence of a cranial defect

Who the study is looking for

  • Patients with age group 45 to 65
  • Both genders
  • Patients with stroke that was diagnosed clinically and/ or by computed tomography (CT) or magnetic resonance imaging
  • Patient with stable vital signs and GCS score \>8-15
  • Patients with mini mental state examination score\>24(30)

Age in the registry: 45 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
Muhammad kashif
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

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