The Effect of Core Exercises in Postoperative Scoliosis
3 juni 2026 uppdaterad av: Feride FEHİM, Hasan Kalyoncu University
The Effect of Core Stabilization Exercises on Scapular and Shoulder Asymmetry in Postoperative Adolescent Idiopathic Scoliosis.
This study aims to investigate the effects of a core stabilization-based rehabilitation program following adolescent idiopathic scoliosis (AIS) surgery on radiological parameters, pain, upper extremity function, range of motion, and scapular assessment.
Participants diagnosed with AIS and treated with posterior spinal fusion surgery will undergo a rehabilitation program based on core stabilization exercises.
Outcome measures will include Cobb angle, vertebral rotation, Visual Analog Scale (VAS), QuickDASH, Trunk Appearance Perception Scale (TAPS), SRS-22, cervical and shoulder range of motion, and scapular assessment tests.
Assessments will be conducted before and after the rehabilitation program.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This study is designed to investigate the effects of a core stabilization-based rehabilitation program following adolescent idiopathic scoliosis (AIS) surgery on radiological, functional, and scapular parameters. Individuals diagnosed with AIS and treated with posterior spinal fusion surgery will be recruited for participation.
Radiological assessment will include thoracic and lumbar Cobb angles and vertebral rotation measurements. Clinical assessments will include the Visual Analog Scale (VAS) for pain, QuickDASH for upper extremity function, Trunk Appearance Perception Scale (TAPS) for body image perception, and SRS-22 for health-related quality of life. Cervical and shoulder range of motion will also be evaluated.
Scapular assessment will include the Lateral Scapular Slide Test (LSST), Scapular Assistance Test (SAT), and wall push-up test. The study aims to evaluate changes in scapular asymmetry, scapular control, and scapulothoracic mechanics following the rehabilitation program.
Assessments will be performed before and after the intervention to examine potential changes in radiological, functional, and scapular outcomes.
Studietyp
Interventionell
Inskrivning (Faktisk)
20
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
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Gaziantep, Turkiet (Türkiye)
- Hasan Kalyoncu University
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Barn
- Vuxen
Tar emot friska volontärer
Nej
Beskrivning
Inclusion Criteria:
- Individuals diagnosed with adolescent idiopathic scoliosis (AIS)
- Individuals who underwent posterior spinal fusion surgery
- Age between 10 and 18 years
- Individuals participating in a core stabilization-based rehabilitation program
- Individuals who agreed to participate voluntarily
Exclusion Criteria:
- Presence of neurological, rheumatological, or other orthopedic disorders affecting posture or upper extremity function
- History of additional spinal surgery
- Cognitive impairment preventing participation in evaluations
- Incomplete assessment data
- Noncompliance with the rehabilitation program
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: Core Stabilization Rehabilitation Group
Participants received a core stabilization-based rehabilitation program after adolescent idiopathic scoliosis surgery.
The program included core stabilization, postural control, and scapular stabilization exercises
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Participants received a core stabilization-based rehabilitation program following adolescent idiopathic scoliosis surgery.
The rehabilitation program included core stabilization exercises, postural control training, scapular stabilization exercises, and functional exercise approaches.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Scapular Assessment
Tidsram: 10 weeks
|
Scapular control and asymmetry were evaluated using the Lateral Scapular Slide Test (LSST), Scapular Assistance Test (SAT), and wall push-up test.
LSST measures scapular asymmetry by assessing the distance between the scapula and spinal landmarks at different arm positions.
Greater side-to-side differences indicate increased scapular asymmetry.
SAT evaluates improvement in symptoms and scapular motion during assisted scapular upward rotation.
The wall push-up test was used to assess scapular winging and scapular stability.
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10 weeks
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Visual Analog Scale (VAS)
Tidsram: 10 weeks
|
Pain intensity was evaluated using the Visual Analog Scale (VAS).
The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain.
Lower scores indicate reduced pain intensity.
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10 weeks
|
Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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QuickDASH Score
Tidsram: 10 weeks
|
Upper extremity function was assessed using the QuickDASH questionnaire.
Scores range from 0 to 100, with higher scores indicating greater disability and poorer upper extremity function.
Lower scores indicate functional improvement.
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10 weeks
|
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TAPS Score
Tidsram: 10 weeks
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Body image perception was evaluated using the Trunk Appearance Perception Scale (TAPS).
Scores range from 1 to 5, with higher scores indicating better perception of trunk appearance and lower deformity perception.
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10 weeks
|
|
SRS-22 Quality of Life Score
Tidsram: 10 weeks
|
Quality of life was assessed using the Scoliosis Research Society-22 questionnaire (SRS-22).
The questionnaire evaluates pain, self-image, function, mental health, and satisfaction.
Higher scores indicate better quality of life.
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10 weeks
|
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Range of Motion
Tidsram: 10 weeks
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Cervical and shoulder range of motion measurements were evaluated using goniometric assessment.
Higher values indicate greater joint mobility and flexibility.
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10 weeks
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Radiological Parameters
Tidsram: 10 weeks
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Vertebral rotation measurements were evaluated radiologically.
Lower rotation values indicate reduced spinal deformity.
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10 weeks
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Huvudutredare: Yavuz Yakut, Prof. Dr., Hasan Kalyoncu University
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
28 maj 2025
Primärt slutförande (Faktisk)
30 april 2026
Avslutad studie (Faktisk)
30 april 2026
Studieregistreringsdatum
Först inskickad
26 maj 2026
Först inskickad som uppfyllde QC-kriterierna
3 juni 2026
Första postat (Faktisk)
8 juni 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
8 juni 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
3 juni 2026
Senast verifierad
1 juni 2026
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- HasanKU-FTR-FF-01
Plan för individuella deltagardata (IPD)
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NEJ
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