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Completed

NCT Number: NCT07610889

Effects of Motor Imagery Technique With and Without Virtual Reality on Pain Intensity ,Functional Disability and Quality of Life in Patient With Post Stroke Shoulder Hand Syndrome

the current study is a randomized controlled trial comparing the effectiveness of motor imagery techanique with and without virtual reality on pain intensity , functional disability and quality of life for individual with post stroke shoulder hand syndrome . this trial aims to evaluate pain , functional disability and overall quality of life . the primary outcome is pain reduction . while seconday outcome reduce disability and improve quality of life .the hypothesis is that the combination of motor imagery and virtual reality will result in significant greater clinical improvement compared to motor imagery alone .

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Key information

Age range

40 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Green International Univeristy

Lahore, Punjab Province, 54000, Pakistan

About this study

Stroke continues to be one of the most common neurological causes of long term disability across the world. It often leads to a wide range of sensory, motor, and cognitive impairments that significantly reduce independence and quality of life. Among the various secondary complications that follow a stroke, Shoulder Hand Syndrome is considered one of the most painful and disabling conditions. It is described as a condition that presents with severe shoulder pain, hand edema, joint stiffness, reduced range of motion, and progressive functional decline. The condition is also known as Complex Regional Pain Syndrome Type One after stroke and it commonly develops within the first few months of the neurological injury. Estimates suggest that the condition affects between twelve to thirty percent of stroke survivors and is associated with marked disability if not treated in a timely and effective manner.Traditional physical therapy approaches such as range of motion exercises, manual therapy, strengthening, and functional task training remain the foundation of treatment. However, these interventions are often limited when patients experience severe pain or fear of movement, which prevents active participation. This has created a need for interventions that can stimulate the brain and support motor recovery without requiring significant physical effort or causing pain. One such approach is motor imagery. Motor imagery is described as the mental rehearsal of movement without any actual execution of the movement. During motor imagery practice, the individual imagines performing a movement as vividly as possible while staying in a relaxed state.hile traditional motor imagery has been widely studied, the use of virtual reality as an adjunct tool has expanded rapidly in recent years. Virtual reality based rehabilitation offers an immersive and engaging environment where the patient experiences visual and sensory feedback that closely resembles real movement. The use of virtual reality enhances motivation, increases concentration, and improves patient satisfaction during therapy sessions. Most importantly, virtual reality supports the activation of mirror neuron pathways and enhances sensory motor integration, which are critical components of recovery after a stroke.The intervention for both groups was delivered over a structured six week period. Each participant attended therapy three days per week, and every session last for a total of thirty minutes. This schedule is designed to provide consistent therapeutic exposure while preventing fatigue and allowing adequate recovery between sessions. By maintaining the same duration and frequency for both groups, the study ensured that any differences in outcomes can be attributed to the type of motor imagery intervention rather than differences in treatment time.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Post-stroke patients diagnosed with Shoulder-Hand Syndrome
  • Age 40-70 years
  • Both males and females
  • Ability to understand motor imagery tasks
  • Duration of stroke ≥ 3 months

Exclusion criteria

  • Cognitive impairment
  • Severe visual deficits
  • Psychiatric illness
  • Pain medication changes during study
  • Uncontrolled medical conditions

Treatment and study plan

motor imagery with virtual reality

Other

participants will receive 30 minute intervention session .the integrated components consist of motor imagery and virtual reality followed by the application of affected arease

motor imagery alone

Other

participant will receive same 30 minutes session of specializes motor imagery techniques . no virtual reality sessions are included

Primary outcomes

  1. PAIN INTENSITY

    Time frame: three session per week for sic weeks

    numeric pain rating scale is used to measure pain by rating one to ten according to the severity of the pain .

    scale level from 0 to 10

    o means no pain 10 means higher level of pain

Other outcomes

  1. disability

    Time frame: three times a week for six week

    shoulder pain and disability index (SPADI) use to measure level of disability at baseline and after intervention. the scale have scoring from 0 to 100 .

    0 to 20 means mild shoulder pain and disability 21 to 40 means moderate shoulder pain and disability 41 to 60 means severe shoulder pain and disability 61 to 80 means very severe shoulder pain and disability 81 to 100 means extremely severe shoulder pain and disability

Sponsors and collaborators

Lead sponsor

Green International University

Other

Registry information

Acronym: VR-SHS

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 28, 2026
Registry last updated
May 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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