BSPTS and Core Stabilization Exercises in Adolescents With Idiopathic Scoliosis
8. august 2026 oppdatert av: Yunus Emre Tutuneken, Istinye University
Effects of Core Stabilization Exercises Combined With Barcelona Scoliosis Physical Therapy School Exercises on Trunk Rotation Angle and Core Muscle Endurance in Individuals With Adolescent Idiopathic Scoliosis: A Randomized Controlled Study
This study aims to investigate the short-term effects of adding core stabilization exercises to Barcelona Scoliosis Physical Therapy School (BSPTS) exercises in adolescents with idiopathic scoliosis.
Participants will be randomly assigned to either a BSPTS exercise group or a BSPTS plus core stabilization exercise group.
Both groups will participate in supervised exercise sessions twice a week for 6 weeks.
The study will evaluate changes in trunk rotation angle and core muscle endurance as the primary outcomes, as well as dynamic balance, spinal appearance perception, postural awareness, and scoliosis-related quality of life.
Studieoversikt
Status
Har ikke rekruttert ennå
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
36
Fase
- Ikke aktuelt
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
Nei
Beskrivelse
Inclusion Criteria:
- Diagnosis of adolescent idiopathic scoliosis.
- Cobb angle between 10° and 40°.
- Risser sign between 0 and 3.
- Ability to understand and perform the exercise instructions.
- Willingness to participate in the study and provision of informed consent.
Exclusion Criteria:
- Scoliosis associated with congenital, neuromuscular, or syndromic conditions.
- Previous spinal surgery.
- Presence of significant lower-extremity deformity or neurological disorder affecting balance or exercise performance.
- Current participation in another scoliosis-specific exercise program.
- Severe cardiopulmonary or systemic disease contraindicating exercise.
- Inability to complete the assessment procedures or exercise program.
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: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: BSPTS Plus Core Stabilization Exercise Group
|
Participants will receive the same BSPTS-based scoliosis-specific exercise program, combined with core stabilization exercises targeting activation of the transversus abdominis, multifidus, and other deep trunk muscles.
Sessions will be conducted under the supervision of a physiotherapist for 45 minutes, twice weekly for 6 weeks.
|
|
Aktiv komparator: BSPTS Exercise Group
|
Participants will receive a Barcelona Scoliosis Physical Therapy School (BSPTS)-based scoliosis-specific exercise program.
The program will include three-dimensional self-correction exercises focusing on spinal elongation, derotation, and sagittal plane alignment.
Sessions will be conducted under the supervision of a physiotherapist for 45 minutes, twice weekly for 6 weeks.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Trunk Rotation Angle
Tidsramme: Baseline and immediately after the 6-week intervention.
|
Trunk rotation angle measured using a scoliometer during the Adams Forward Bend Test.
|
Baseline and immediately after the 6-week intervention.
|
|
Core Muscle Endurance
Tidsramme: Baseline and immediately after the 6-week intervention.
|
Core muscle endurance assessed using the McGill Core Endurance Test Battery, including trunk flexor, trunk extensor, and right and left lateral plank tests.
|
Baseline and immediately after the 6-week intervention.
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Dynamic Balance
Tidsramme: Baseline and immediately after the 6-week intervention.
|
Dynamic balance assessed using the Y-Balance Test.
|
Baseline and immediately after the 6-week intervention.
|
|
Spinal Appearance Perception
Tidsramme: Baseline and immediately after the 6-week intervention.
|
Spinal appearance perception assessed using the Spinal Appearance Questionnaire (SAQ).
|
Baseline and immediately after the 6-week intervention.
|
|
Postural Awareness
Tidsramme: Baseline and immediately after the 6-week intervention.
|
Postural awareness assessed using the Postural Awareness Scale (PAS).
|
Baseline and immediately after the 6-week intervention.
|
|
Scoliosis-Related Quality of Life
Tidsramme: Baseline and immediately after the 6-week intervention.
|
Quality of life, functional status, and psychosocial impact assessed using the Scoliosis Research Society-22 (SRS-22) questionnaire.
|
Baseline and immediately after the 6-week intervention.
|
|
Global Perceived Change
Tidsramme: Immediately after the 6-week intervention.
|
Perceived change following treatment assessed using the Global Rating of Change Scale.
|
Immediately after the 6-week intervention.
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
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)
20. august 2026
Primær fullføring (Antatt)
25. mars 2027
Studiet fullført (Antatt)
25. mars 2027
Datoer for studieregistrering
Først innsendt
8. august 2026
Først innsendt som oppfylte QC-kriteriene
8. august 2026
Først lagt ut (Faktiske)
12. august 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
12. august 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
8. august 2026
Sist bekreftet
1. august 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- 103
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