Actively Recruiting

Phase Not Applicable
Age: 40Years - 60Years
All Genders
NCT06196229

Effects of Action Observation Therapy Based on Virtual Reality for Upper Extremity Rehabilitation in Stroke

Led by Riphah International University · Updated on 2024-06-26

36

Participants Needed

1

Research Sites

31 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to conduct a randomized controlled trial (RCT) assessing the effectiveness of combining Action Observation (AO) with Virtual Reality (VR) in improving upper limb function for stroke patients compared to AO therapy alone. Individuals who meet the inclusion criteria will be assigned by lottery into one of two groups: Group A will receive only AO therapy, watching daily actions and then executing them, while Group B will receive both AO and VR therapy, using VR glasses to complete tasks. The Box and Block Test for manual dexterity, the Timed Test, the Modified Ashworth Scale for spasticity, the Rankin Scale for symptom severity, and the Fugl-Meyer Assessment for motor, balance, sensation, and joint function will all be used in the evaluation, both before and after the intervention. Every participant will go through 18 sessions totaling 60

CONDITIONS

Official Title

Effects of Action Observation Therapy Based on Virtual Reality for Upper Extremity Rehabilitation in Stroke

Who Can Participate

Age: 40Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or Female participants
  • Age between 40 and 60 years
  • Unilateral upper limb weakness from stroke confirmed by neurological exam
  • Residual movement in affected upper limb with Medical Research Council (MRC) index greater than 2 and less than 4
  • Mini-Mental State Examination (MMSE) score of 27 or higher
  • Able to cooperate and understand the activities in the study
Not Eligible

You will not qualify if you...

  • Severe cognitive impairment with MMSE score below 20
  • Severe unilateral spatial neglect as measured by Bells Test
  • Severe ideomotor apraxia
  • Severe anosognosia
  • Severe language comprehension problems
  • Untreated severe psychiatric disorders
  • Sensory impairments or uncorrected visual deficits that affect participation
  • Drug-resistant epilepsy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Riphah International University

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

I

Imran Amjad, Phd

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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