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Effect of Pelvic Floor Muscle Training Combined With Scoliosis-Specific Three-Dimensional Exercises in Adolescents With Idiopathic Scoliosis

NCT07742670 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2026-08-04

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the effects of scoliosis-specific three-dimensional exercises combined with pelvic floor muscle training on scoliosis severity and spinopelvic parameters in adolescents with idiopathic scoliosis. The main questions it aims to answer are:

* Does the addition of pelvic floor muscle training to scoliosis-specific three-dimensional exercises improve scoliosis severity compared with scoliosis-specific three-dimensional exercises alone?
* Does the addition of pelvic floor muscle training improve spinopelvic parameters compared with scoliosis-specific three-dimensional exercises alone? Researchers will compare a scoliosis-specific three-dimensional exercise plus pelvic floor muscle training group with a scoliosis-specific three-dimensional exercise group to determine whether the combined intervention provides additional clinical benefits.

Participants will:

* undergo baseline clinical and radiographic assessments;
* be randomly assigned to one of the two intervention groups;
* receive supervised treatment for 3 months according to the assigned intervention;
* undergo follow-up clinical and radiographic assessments at the end of the intervention period.

Conditions

  • Scoliosis Idiopathic Adolescent
  • Scoliosis,Idiopathic,Adolescent

Interventions

BEHAVIORAL

Scoliosis-Specific Three-Dimensional Exercise

Supervised scoliosis-specific three-dimensional exercises administered twice weekly for 3 months, with additional home exercises according to the study protocol.

BEHAVIORAL

Pelvic Floor Muscle Training

Supervised pelvic floor muscle training performed in combination with scoliosis-specific three-dimensional exercises twice weekly for 3 months, with additional home exercises according to the study protocol.

Sponsors & Collaborators

  • Gazi University Scientific Research Unit

    collaborator UNKNOWN

  • Gazi University

    lead OTHER

Principal Investigators

  • Selda Başar, PhD · Gazi University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-12
Primary Completion
2026-10-31
Completion
2026-10-31

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 NCT07742670 on ClinicalTrials.gov