Synergic Effects of Schroth Method With and Without Core Stabilization Exercises in Idiopathic Scoliosis Patients

University of Lahore

Status: Enrolling

Conditions: Scoliosis; Scoliosis Idiopathic

Treatments: Other: Schroth Method; Other: Schroth Method with Core Stabilization Exercises

Study type: Interventional

Funder types: Other

Identifiers

NCT07059663

Faiza.sarwar

Details and patient eligibility

About

A randomized controlled trial was conducted on 72 patients diagnosed with idiopathic scoliosis at the University of Lahore Teaching Hospital. The study aimed to explore the synergistic effects of the Schroth method with and without core stabilization exercises. Participants were randomly allocated into two groups: Group A, which received both the Schroth method and core stabilization exercises, and Group B, which received only the Schroth method. The intervention lasted for 10 weeks, with assessments conducted at baseline, the 5th week, and the 10th week. Outcome measures included Cobb angle (spinal curvature), lumbar extensor endurance (Sorensen test), chest mobility, and quality of life (SRS-22 questionnaire). The study found significant improvements in all outcome measures for both groups, with Group A showing superior results. The addition of core stabilization exercises to the Schroth method resulted in better reductions in Cobb angle, enhanced lumbar extensor endurance, and improved chest mobility and quality of life, indicating a synergistic effect of the combined approach. The findings suggest that incorporating core stabilization exercises into scoliosis treatment protocols can lead to superior clinical outcomes.

Full description

A randomized controlled trial will be conducted at the University of Lahore Teaching Hospital. Thirty patients diagnosed with idiopathic scoliosis, aged 10 to 18 years, will be randomly divided into two groups: Group A will receive the Schroth method in combination with core stabilization exercises, while Group B will receive only the Schroth method. Both interventions will be delivered three times weekly for ten weeks. Outcome measures, including Cobb angle (curve magnitude), lumbar extensor endurance (Sorensen test), chest mobility, and quality of life (SRS-22), will be assessed at baseline, week 5, and week 10.

Enrollment: 72 estimated patients

Sex: All

Ages: 10 to 18 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• • Age 10 to 18

  • X-ray diagnosed of idiopathic scoliosis with Cobb Angle 10˚- 30˚
  • Participants with Idiopathic Scoliosis
  • Both genders will be included
  • Scoliosis with Down syndrome.

Exclusion criteria

• Any neurological condition such as cerebral palsy or epilepsy.
• Any other orthopedic condition such as hip dysplasia, osteogenesis imperfecta, or leg length discrepancy.
• Surgical history of the spine, such as spinal fusion and decompression surgery.
• Severe systemic disorders such as autoimmune disorders, severe cardiovascular conditions
• Non-Idiopathic Scoliosis

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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72 participants in 2 patient groups

Schroth method with Core Stabilization Exercises

Experimental group

Description:

The Schroth method and core stabilization exercises will be performed three times a week for 10 weeks, with each session lasting 60 minutes

Treatment:

Other: Schroth Method with Core Stabilization Exercises

Schroth Method

Active Comparator group

Description:

this group will receive the core stabilization exercises alone

Treatment:

Other: Schroth Method