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Investigation of Muscle Activity With sEMG, Surface Topography and Radiographic Changes of Paraspinal Muscles in Individuals With Adolescent Idiopathic Scoliosis.

3. september 2026 oppdatert av: Kadriye Tombak, Akdeniz University

Investigation of Muscle Activity, Surface Topography and Radiographic Changes of Paraspinal Muscles in Individuals With Adolescent Idiopathic Scoliosis.

The aim of this study is to examine paraspinal muscle activity, body surface topography, posture, and radiographic characteristics in adolescents with idiopathic scoliosis. Adolescents with idiopathic scoliosis who use a brace and those who do not will be compared with healthy individuals. Paraspinal muscle activity will be assessed using surface electromyography (sEMG), surface topography using the Artec Eva 3D scanner, postural characteristics using postural analysis, and spinal curvature using the Cobb angle measurement based on existing radiographs. Quality of life will be assessed using the SRS-22 questionnaire.

Studieoversikt

Status

Har ikke rekruttert ennå

Detaljert beskrivelse

This study was designed to examine paraspinal muscle activity, surface topography, and radiographic characteristics in adolescents with idiopathic scoliosis. The study plans to include adolescents aged 10-18 years diagnosed with idiopathic scoliosis, as well as healthy volunteers matched for age and gender.

Participants will be divided into three groups: adolescents with idiopathic scoliosis who wear a brace, adolescents with idiopathic scoliosis who do not wear a brace, and a healthy control group. A total of 45 participants are planned to be included in the study, with 15 participants in each group.

As part of the study, participants' demographic information will be recorded. Muscle activity in the paraspinal muscles will be assessed using surface electromyography (sEMG). Body surface topography will be assessed using an Artec Eva 3D scanner. Posture analysis will be performed, and spinal curvature will be assessed using the Cobb angle based on existing radiographic images. Quality of life will be determined using the Scoliosis Research Society-22 (SRS-22) questionnaire.

The measurement results obtained will be compared across groups, and the relationships between muscle activity, surface topography, postural characteristics, radiographic parameters, and quality of life will be evaluated.

As part of this study, participants will not receive any treatment or rehabilitation interventions; measurements will be taken to assess their current clinical and physical characteristics.

Studietype

Observasjonsmessig

Registrering (Antatt)

45

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

  • Barn
  • Voksen

Tar imot friske frivillige

Ja

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

The study population will consist of adolescents with adolescent idiopathic scoliosis who are referred to the rehabilitation program by a specialist physician, including individuals who use a brace and those who do not use a brace, as well as healthy control individuals who meet the eligibility criteria.

Beskrivelse

  • Be between the ages of 10 and 18
  • Have been diagnosed with adolescent idiopathic scoliosis
  • Be able to stand independently
  • Sign the informed consent form
  • Have no spinal deformity (for the control group)
  • History of neurological disease
  • History of spinal surgery
  • Presence of congenital or traumatic scoliosis
  • Presence of orthopedic or rheumatological conditions that could affect the measurements
  • Inability to cooperate during the measurements

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Study Participants
The study participants include adolescents with adolescent idiopathic scoliosis, including individuals who use a brace and those who do not use a brace, as well as healthy control individuals who meet the eligibility criteria.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Paraspinal Muscle Activity
Tidsramme: Baseline (single assesment)
Paraspinal muscle activity will be assessed using surfaces electromyography (sEMG) in adolescents with adolescent idiopathic scoliosis and healthy controls.
Baseline (single assesment)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Surface Topography
Tidsramme: Baseline (single assesment)
Surface topography will be assessed to evaluate trunk surface characteristics in adolescents with adolescent idiopathic scoliosis and healthy controls.
Baseline (single assesment)
Radiographic Parameters
Tidsramme: Baseline (single assesment)
Radiographic parameters will be evaluated to assess spinal alignment in adolescents with adolescent idiopathic scoliosis.
Baseline (single assesment)

Samarbeidspartnere og etterforskere

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

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)

1. september 2026

Primær fullføring (Antatt)

1. juni 2027

Studiet fullført (Antatt)

1. september 2027

Datoer for studieregistrering

Først innsendt

31. august 2026

Først innsendt som oppfylte QC-kriteriene

3. september 2026

Først lagt ut (Faktiske)

4. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

4. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • Paraspinal muscles for AIS

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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