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Идёт набор NCT05819034

Conservative Management for Adolescent Idiopathic Scoliosis

Без фазы С лечением Scoliosis; Adolescence

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Scoliosis-Specific Exercise Program, Soft orthoses with external strapping..
Кому может быть актуально
Состояния в реестре: Scoliosis; Adolescence. Базовые параметры: 10 лет — 17 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Саудовская Аравия
Следующий шаг
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Официальное название

Orthotic Management for Controlling Scoliotic Curve Progression in Adolescent Idiopathic Scoliosis

Обзор

Idiopathic scoliosis is a living problem that resists correction. The underlying cause of the such disorder is unknown but directed more toward muscular disorders. However recent clinical observation showed a possible neuromuscular compromise early in those patients. The main purpose of this study is to develop a treatment procedure to correct the degree of bony curvature in patients with Idiopathic scoliosis through developing a neuromuscular corrective approach that might be a more effective conservative treatment protocol for such disorder.

Подробное описание

Scoliosis is one of the most common spinal deformities occurring in school-going children during the growth spurts of adolescents. It is an abnormal curvature of the spine. Failure of early management of idiopathic scoliosis could lead to multiple problems related to postural malalignment, pulmonary and physical dysfunctions, and surgical interventions. These problems could lead to health-related quality-of-life issues such as psychological and social problems that are represented in social isolation, depression, loss of self-confidence, limited job opportunities, and hospital stays \& days off school and university as a result of undergoing corrective surgeries. Treatment methods for adolescent idiopathic Scoliosis (AIS) vary between surgical intervention and conservative treatment, in mild and moderate cases. Conservative treatment includes physical therapy in addition to rigid splints and braces, which may cause pain, tightness, restriction of movement, and a bad psychological status for adolescents which may lead them to the irregular wearing of these splints and braces. A type of soft, lightweight, breathable orthosis which is TheraTogs orthotic undergarment with the strapping system has been fabricated to provide gentle, passive compression to correct spinal deformities. Therefore, the objective of this study is to evaluate the effectiveness of TheraTogs orthotic undergarment with the strapping system on controlling and modulating the degree of scoliosis in Saudi adolescents with idiopathic scoliosis.

Вмешательства

  • Другое Scoliosis-Specific Exercise Program
    Adolescents in the control group will receive a scoliosis-specific exercise program which will be prescribed to control the progression of the scoliotic curve. This exercise program will include frontal plane active or passive correction exercises for scoliotic posture. The exercise program for every participant will be three sessions per week for 12 successive weeks. Every treatment session was applied for one hour.The exercise program for every participant will be three sessions per week for 1
  • Другое Soft orthoses with external strapping.
    Adolescents in the experimental group will receive a scoliosis-specific exercises program which will be prescribed to control the progression of the scoliotic curve in addition to wearing the soft orthoses with external strapping. The wearing schedule of the soft orthosis with the external strapping for every participant in this group will be 12 hours daily for 12 successive weeks.

Первичные конечные точки

  • Change in the scoliotic cobb's angle (°) [Срок оценки: [Data was collected at baseline, and 12 weeks after intervention commencement.]]
  • Changes in the Pelvic Obliquity (mm) [Срок оценки: [Data was collected at baseline, and 12 weeks after intervention commencement.]]
  • Change in the vertebral rotation (Angle) [Срок оценки: [Data was collected at baseline, and 12 weeks after intervention commencement.]]
  • Change in the Coronal imbalance (mm) [Срок оценки: [Data was collected at baseline, and 12 weeks after intervention commencement.]]

Критерии участия

The inclusion criteria will be:

  • Adolescents of both sexes with an age range between 10-17 years.
  • They were diagnosed with Adolescent idiopathic scoliosis by an orthopedic specialist, confirmed through (loaded) X- rays.
  • They have mild non-structural scoliosis with Cobb's angle measurement of between 10 and 25 degrees
  • They have Single major thoracolumbar curve located between T6-7 to L1-2, apex at T12 or L1.
  • They have good health conditions except for scoliosis.
  • They can understand and communicate with no mental abnormalities.

The exclusion criteria will be:

  • Adolescents with cerebral palsy or other degenerative neurological disorders;
  • Participants with nutritional disorders e.g. diabetes or vascular disorders.
  • Participants with a scoliotic curve with angle > 25° will be excluded.
  • Participants will be excluded from this study if they have inflexible spinal deformities interfering with spinal mobility,
  • Participants who were subjected to any corrective surgery to their spine within the previous two years.
  • Participants will be also excluded if their skin were sensitive or inflamed to any materials used.
  • Participants who have seizures, perceptual disorders, visual problems, and auditory deficits
  • Participants who have leg length discrepancy
  • Participants who have scoliosis developed as a consequence of traumatic scoliosis.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Лечение

Центры проведения

Саудовская Аравия · 1 центр
  • Umm Al Qura University — Mecca

Идентификаторы

NCT: NCT05819034 · DSR02

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗