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RecruitingNCT07177430

Inspiratory Muscle Training in Children and Adolescents With Idiopathic Scoliosis Undergoing Schroth Therapy.

The Effect of Inspiratory Muscle Training on Respiratory Function, Exercise Tolerance and Core Stability in Children and Adolescents With Idiopathic Scoliosis Undergoing Schroth Therapy.

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
56 (estimated)
Sponsor
Wroclaw University of Health and Sport Sciences · Academic / Other
Sex
All
Age
11 Years – 16 Years
Healthy volunteers
Not accepted

Summary

This study evaluates the effectiveness of inspiratory muscle training in children and adolescents with idiopathic scoliosis undergoing therapy with the Schroth method. The intervention- inspiratory muscle training- aims to improve respiratory function, increase exercise tolerance, and strengthen core stability in the participants. The proposed training may enhance the effectiveness of therapy conducted using the Schroth method and improve participants' performance in activities of daily living. The project aims to assess the impact of inspiratory muscle training in children and adolescents with idiopathic scoliosis on respiratory system function, exercise tolerance, and core stability.

Conditions

Interventions

TypeNameDescription
DEVICEInspiratory Muscle TrainingParticipants will perform inspiratory muscle training using a respiratory muscle trainer. The initial training load will be set at 30% of PImax. The intervention will last for 8 weeks and will be carried out 5 days per week, twice daily, in 3 sets of 10 repetitions. The training load will be increased in the 2nd, 4th, and 6th week of the program, each time by an additional 10% relative to the initial PImax.
DEVICEInspiratory Muscle Training (Sham)The training intervention in the Sham Group will differ from the experimental group only in terms of training load. This load will remain constant at 15% PImax, which does not cause any changes in the functioning of the inspiratory muscles. All other training parameters will be identical to those in the IMT group.

Timeline

Start date
2025-10-13
Primary completion
2027-05-01
Completion
2027-07-01
First posted
2025-09-17
Last updated
2025-12-05

Locations

2 sites across 1 country: Poland

Source: ClinicalTrials.gov record NCT07177430. Inclusion in this directory is not an endorsement.