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Clinical Trials/NCT06520748
NCT06520748
Completed
Not Applicable

IMPACT OF COMPUTERIZED GLOVE ON FACILITATING HAND FUNCTION RECOVERY AND NEURAL PLASTICITY IN PATIENT WITH STROKE

Ahmed Alshimy1 site in 1 country30 target enrollmentOctober 5, 2023
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Ahmed Alshimy
Enrollment
30
Locations
1
Primary Endpoint
Quantitive Electro Encephalo Graphy
Status
Completed
Last Updated
last year

Overview

Brief Summary

Hand impairment post-stroke is a common condition that contributes to disability around the world. An effective intervention is required to optimize functional outcomes in the rehabilitation of hand-in-stroke patients.

Detailed Description

Thirty male/female stroke patients in the sub-acute phase were randomly assigned in to the two groups (study and control) in sets of three. The study group (A) (n = 15) underwent a hand rehabilitation program using the computerized glove combined with the selected hand program. The control group (B) (n = 15) received only the selected hand program. The treatment schedules for 18 consecutive treatment sessions, three times per week.

Registry
clinicaltrials.gov
Start Date
October 5, 2023
End Date
April 3, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Sponsor
Ahmed Alshimy
Responsible Party
Sponsor Investigator
Principal Investigator

Ahmed Alshimy

Lecturer of Physical Therapy for Neurology and it's Surgery

AlRyada University for Science & Technology

Eligibility Criteria

Inclusion Criteria

  • The patient's age ranges from 45 to 65 years old with a minimum score of 24 points on the Mini Mental Test.
  • Duration of illness ranges from (6weeks to 6 months) after stroke onset.
  • first stroke.
  • Upper limb spasticity ranged from 1+ to 2 according to the Modified Ashworth Scale.
  • With a minimum 10° extension and/or flexion of the wrist or fingers, an ability to flex and extend the wrist joint five times continuously without losing active range of motion.

Exclusion Criteria

  • Patients with the following
  • apraxia or hemianopsia.
  • diabetic polyneuropathy.
  • Aphasia , cognitive deficits.
  • a previous disability in the upper limbs, tactile agnosia (stereognosis).
  • LT hemiplegia, Post Botox injection, recurrent stroke, and Posterior parietal lesion.

Outcomes

Primary Outcomes

Quantitive Electro Encephalo Graphy

Time Frame: 6 weeks

Used to assess Neuralplasticity (sleep Delta - Delta/Beta ratio )

Computerized glove software

Time Frame: 6 weeks

Used to assess the Kinematic Data (Thumb, Index, Middle, ring, little, and average range of motion)

Action Research Arm Test

Time Frame: 6 weeks

Used to assess Fine manual dexterity

Study Sites (1)

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