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The Effects of Schroth Based Exercise Therapy in Adolescents with Pectus Excavatum

The Effects of Schroth Based Exercise Therapy in Adolescents with Pectus Excavatum

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06763406
Enrollment
35
Registered
2025-01-08
Start date
2023-04-15
Completion date
2024-05-01
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chest Deformities, Funnel Chest, Pectus Excavatum, Pectus Excavatum Deformity

Keywords

Funnel chest, Pectus excavatum, Exercise, Exercise therapy, Vacuum, Tissue expansion devices

Brief summary

Research on exercise methods for pectus excavatum (PE) is limited, highlighting the need for further studies. This study investigated the effects of Schroth-based exercise therapy combined with vacuum treatment in 35 adolescents with PE, divided into a vacuum + exercise group (n=19) and a vacuum-only group (n=16). Outcomes included deformity severity, sagittal posture, thoracic cage and spinal mobility, muscle endurance, and quality of life. The combination therapy significantly improved sagittal spinal posture (craniovertebral, thoracic, thoracolumbar, lumbar angles) and deformity-specific quality of life (Nuss Questionnaire scores) compared to vacuum-only treatment.

Interventions

OTHERExercise

Due to the limited research on exercise approaches for pectus excavatum, further investigation in this field is needed. This study aims to explore the impact of Schroth-based exercise therapy on adolescents with pectus excavatum.

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* having pectus excavatum * being 10-18 years * having Haller index more than 2.5

Exclusion criteria

* Individuals with pectus excavatum associated with a syndrome Individuals with mixed deformity * Individuals who have previously received any conservative treatment or surgery for chest deformity or spinal issues * Individuals with neuromuscular, rheumatic, or chronic systemic diseases

Design outcomes

Primary

MeasureTime frameDescription
Primary Outcome Measure 1: Deformity Severity12 weeksPrimary Outcome Measure 1: Deformity Severity Measurement: Anthropometric Index (cm) Details: Repeated, in cm. Time frame: The assessment will be conducted during the first week of treatment and 12 weeks after treatment
Primary Outcome Measure 2: Sagittal Spinal Posture12 weeksPrimary Outcome Measure 2: Sagittal Spinal Posture Measurement: Lateral Photos (°) Details: In degrees Time Frame:The assessment will be conducted during the first week of treatment and 12 weeks after treatment
Primary Outcome Measure 3: Disease-Specific QoL12 weeksPrimary Outcome Measure 3: Disease-Specific QoL Measurement: Nuss Questionnaire (1-4) Details: Higher = better Time Frame: The assessment will be conducted during the first week of treatment and 12 weeks after treatment
Primary Outcome Measure 4: General QoL12 weeksPrimary Outcome Measure 4: General QoL Measurement: PedsQL (0-100) Details: Higher = better Time Frame: The assessment will be conducted during the first week of treatment and 12 weeks after treatment

Secondary

MeasureTime frameDescription
Secondary Outcome Measure 1: Thoracic Cage Mobility12 weeksSecondary Outcome Measure 1: Thoracic Cage Mobility Measurement: Chest Circumference (cm) Details: In cm Time Frame: The assessment will be conducted during the first week of treatment and 12 weeks after treatment
Secondary Outcome Measure 5: Muscle Endurance (Lateral Bridge)12 weeksSecondary Outcome Measure 5: Muscle Endurance (Lateral Bridge) Measurement: Lateral Bridge (s) Details: Duration Time Frame: The assessment will be conducted during the first week of treatment and 12 weeks after treatment
Secondary Outcome Measure 2: Spinal Mobility12 weeksSecondary Outcome Measure 2: Spinal Mobility Measurement: Sit-and-Reach (cm) Details: Highest value Time Frame: The assessment will be conducted during the first week of treatment and 12 weeks after treatment
Secondary Outcome Measure 3: Lumbar Mobility12 weeksSecondary Outcome Measure 3: Lumbar Mobility - Measurement: Modified Schober (cm) Details: Difference in cm Time Frame: The assessment will be conducted during the first week of treatment and 12 weeks after treatment
Secondary Outcome Measure 4: Muscle Endurance (Sit-Ups)12 weeksSecondary Outcome Measure 4: Muscle Endurance (Sit-Ups) Measurement: Sit-Up (reps/30s) Details: Repetitions Time Frame: The assessment will be conducted during the first week of treatment and 12 weeks after treatment

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026