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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 (VR-SHS)

22. mai 2026 oppdatert av: Muhammad Hammad khan, Green International University
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 .

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

40

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 54000
        • Green International Univeristy

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Trippel

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Motor imagery with virtual reality
participants of shoulder hand syndrome received a combination treatment of motor imagery with virtual reality .both treatment options provided to improve motor function , reduce pain and improve quality of life . provide treatment of both motor imagery and virtual reality
participants will receive 30 minute intervention session .the integrated components consist of motor imagery and virtual reality followed by the application of affected arease
Aktiv komparator: motor imagery alone
participant in this arm will receive only motor imagery treatment protocol . the therapy will target shoulder and hand region to increse ROM , decrease stiffness and pain .
participant will receive same 30 minutes session of specializes motor imagery techniques . no virtual reality sessions are included

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
PAIN INTENSITY
Tidsramme: 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

three session per week for sic weeks

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
disability
Tidsramme: 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

three times a week for six week

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

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Studer hoveddatoer

Studiestart (Faktiske)

2. november 2025

Primær fullføring (Faktiske)

29. april 2026

Studiet fullført (Faktiske)

6. mai 2026

Datoer for studieregistrering

Først innsendt

15. mai 2026

Først innsendt som oppfylte QC-kriteriene

22. mai 2026

Først lagt ut (Faktiske)

28. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

28. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

22. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

only ipd used in the results publication will be shared

IPD-delingstidsramme

it will be available after the completion of study

Tilgangskriterier for IPD-deling

through the corresponding author

IPD-deling Støtteinformasjonstype

  • STUDY_PROTOCOL
  • SEVJE
  • ICF
  • CSR

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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