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Virtual Reality Versus Traditional Exercise on EMG Activity in Postural Malalignment (EMG)

27. september 2026 oppdatert av: Mohamed Abdelmegeed, Hofstra University

Influence of Virtual Reality Versus Traditional Exercise on Trapezius Muscle EMG Activity in Relaxed and Corrected Postures Among Individuals With and Without Postural Malalignment

This study aims to investigate the immediate effects of virtual reality (VR)-based exercise compared with traditional Active free exercise on trapezius muscle activation in adults with and without postural malalignment. Surface electromyography (EMG) will be used to assess upper, middle, and lower trapezius muscle activity during relaxed and corrected postures and during VR and traditional exercise. Demographic data will be collected. The study will also assess posture, trapezius muscle strength, cervical range of motion, Activity level, craniovertebral angle, and neck proprioception. Approximately 40 adults aged 18-35 years will participate in a single study session. The findings may help determine whether VR-based rehabilitation provides an effective and engaging approach for assessing and training postural control and trapezius muscle activation.

Studieoversikt

Detaljert beskrivelse

This study will investigate the immediate effects of virtual reality (VR)-based exercise compared with traditional exercise on trapezius muscle activation in adults with and without postural malalignment. The study will include approximately 40 adults aged 18-35 years. Participants will be classified according to the presence or absence of postural abnormalities and symptoms.

At baseline, demographic and clinical information will be collected, followed by assessment of forward head posture, rounded shoulder posture, trapezius muscle strength, cervical range of motion, Activity level, craniovertebral angle and joint position sense. Forward head posture will be assessed using the craniovertebral angle obtained through digital photogrammetry, while rounded shoulder posture will be evaluated using the acromion-to-table distance. Symptomatic participants will additionally complete the Numeric Pain Rating Scale (NPRS) and Neck Disability Index (NDI).

Surface electromyography (sEMG) will be used to record the activity of the upper, middle, and lower trapezius muscles. EMG activity will be assessed during relaxed and corrected standing postures and continuously during the exercise conditions. EMG data will be normalized to maximum voluntary isometric contraction (MVIC) and expressed as a percentage of MVIC.

Each participant will complete both the VR-based intervention and the traditional TheraBand exercise intervention during a single study session. The VR intervention will be performed using a Virtualis rehabilitation system with an HTC Vive headset and motion controllers and will involve controlled upper-extremity movements designed to promote appropriate scapular and postural control. The traditional exercise condition will include standing active free exercises targeting the upper, middle, and lower trapezius muscles. A rest period will be provided between the two exercise conditions to minimize the potential effects of fatigue.

The primary comparison will examine normalized trapezius muscle activation during the VR-based and active free exercise conditions. Additional assessments will examine posture, trapezius muscle strength, cervical range of motion, and cervical proprioception. The study is intended to provide information regarding the immediate neuromuscular responses to VR-based rehabilitation and its potential application as an interactive approach to postural rehabilitation.

Studietype

Intervensjonell

Registrering (Antatt)

40

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiekontakt

Studer Kontakt Backup

  • Navn: Dina Alhamaky, Ph.D. in Physical Therapy
  • Telefonnummer: +971503963450
  • E-post: dinaali2008@cu.edu.eg

Studiesteder

    • New York
      • Hempstead, New York, Forente stater, 11549
        • Hofstra University

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

18 år til 35 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

participants will include healthy individuals or individuals with postural malalignment.

  • Age 18-35 years
  • Able to provide written informed consent
  • Able to stand and perform light movement tasks safely
  • Normal or corrected-to-normal vision
  • Sufficient intellectual ability to understand and follow instructions
  • Basic English proficiency to understand study instructions and questionnaires
  • For symptomatic participants, presence of postural dysfunction at baseline, including one or more of the following:
  • Forward head posture
  • Rounded shoulder posture

Exclusion Criteria:

  • - Epilepsy
  • Severe balance disorders
  • Major neurological or musculoskeletal conditions
  • Recent injuries
  • Use of medications affecting balance
  • Pregnancy

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: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: VR and Traditional Exercise

Participants will complete both a virtual reality (VR)-based exercise intervention and a traditional exercise intervention during a single study session. Trapezius muscle activity will be recorded using surface electromyography (sEMG) during both exercise conditions, with a rest period provided between interventions to minimize fatigue.

Participants will perform a Virtualis virtual reality rehabilitation activity using an HTC Vive headset and motion controllers while standing. The activity involves controlled upper-extremity reaching movements designed to encourage scapular retraction and depression and maintenance of an upright head and trunk posture. Trapezius muscle activity will be recorded continuously using surface electromyography (sEMG)

Participants will perform standing Active free exercises targeting the upper, middle, and lower trapezius muscles. Exercises will include diagonal arm elevation, horizontal abduction, and shoulder elevation. The duration of exercise during the active free condition will be matched to the duration of the VR intervention. Trapezius muscle activity will be recorded continuously using surface electromyography (sEMG).

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Trapezius Muscle Activation (sEMG)
Tidsramme: During the single study session (approximately 35-45 minutes)

Surface electromyography (sEMG) will be used to measure upper, middle, and lower trapezius muscle activation during the virtual reality and Active free exercise conditions. EMG activity will be normalized to maximum voluntary isometric contraction (MVIC) and expressed as %MVIC.

During the single study session (approximately 35-45 minutes)

Samarbeidspartnere og etterforskere

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

Etterforskere

  • Hovedetterforsker: Mohamed Abdelmegeed, Ph.D. in Physical Therapy, Hofstra University

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

25. oktober 2026

Primær fullføring (Antatt)

25. august 2027

Studiet fullført (Antatt)

25. oktober 2027

Datoer for studieregistrering

Først innsendt

27. september 2026

Først innsendt som oppfylte QC-kriteriene

27. september 2026

Først lagt ut (Faktiske)

2. oktober 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

2. oktober 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

27. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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