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Trunk Proprioception in Adolescent Idiopathic Scoliosis

NCT05326256 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2023-04-19

No results posted yet for this study

Summary

Aims of this clinical research:

* To investigate trunk proprioception in all three planes in individuals with adolescent idiopathic scoliosis (AIS),
* To investigate the pelvis orientation sense in all three planes in individuals with adolescent idiopathic scoliosis,
* To investigate whether trunk proprioception and pelvis orientation sense are improved with Physiotherapy Scoliosis Specific Exercises (PSSE) in AIS,
* To investigate whether trunk proprioception and pelvis orientation sense are improved with vestibular exercise training to be added to PSSE exercises in AIS,
* Comparison of the effects of different exercise training on trunk proprioception and pelvis orientation sense in AIS
* To examine the parameters that may be associated with the improvement of trunk proprioception of different exercise training (health-related quality of life, perception of cosmetic deformity, scoliosis-related clinical features such as Cobb angle, axial trunk rotation, curve type, etc.).

Conditions

  • Scoliosis Idiopathic
  • Scoliosis; Adolescence

Interventions

OTHER

Exercise training- PSSE

Barcelona Scoliosis Physical Therapy School (BSPTS) method exercises

OTHER

Exercise training- PSSE with vestibular exercises

Vestibular exercises added to Barcelona Scoliosis Physical Therapy School (BSPTS) exercises

Sponsors & Collaborators

  • Hasan Kalyoncu University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-02
Primary Completion
2023-02-02
Completion
2023-04-17

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05326256 on ClinicalTrials.gov