Меню
Набор скоро начнётся NCT07318454

Comparison of Abdominal Expansion and Abdominal Drawing-In Training With Manual and Verbal Cueing in Chronic Non-Specific Low Back Pain

Без фазы С лечением Chronic Low Back Pain (Non-specific, Uncomplicated)

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: Abdominal Drawing-In Manoeuvre Training, Dynamic Neuromusculoskeletal Stabilization Abdominal Expansion Training.
Кому может быть актуально
Состояния в реестре: Chronic Low Back Pain (Non-specific, Uncomplicated). Базовые параметры: от 18 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
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

A Randomized Controlled Trial Comparing Abdominal Expansion and Abdominal Drawing-In Training With Manual and Verbal Cueing in Individuals With Chronic Non-Specific Low Back Pain

Обзор

This study aims to investigate the interactive effects of two core stability training strategies-abdominal drawing-in manoeuvre (ADIM) and Dynamic Neuromusculoskeletal Stabilization abdominal expansion (DNS-AE)-and two instructional approaches (verbal cueing and manual facilitation) on training outcomes in individuals with chronic non-specific low back pain. A 2×2 factorial randomized controlled trial design will be employed. Ninety-six participants with chronic non-specific low back pain will be randomly allocated, using block randomization, to one of four intervention groups in equal proportions. All groups will receive a 4-week intervention program, with training conducted twice per week. Outcome measures will be assessed at four time points: before the intervention (baseline), immediately after the first training session, at the completion of the 4-week intervention, and at a 3-month follow-up, to evaluate short-term and mid-term effects as well as the sustainability of training outcomes.

Вмешательства

  • Поведенческое Abdominal Drawing-In Manoeuvre Training
    Abdominal drawing-in manoeuvre (ADIM) training is a core stability exercise strategy emphasizing selective activation and coordination of the deep abdominal musculature to enhance local trunk stability. Participants receive individualized, one-on-one training delivered by licensed physical therapists, conducted twice weekly for 4 weeks. Training is performed across functional positions and task-specific movements, with instruction provided using either verbal cueing or manual facilitation accord
  • Поведенческое Dynamic Neuromusculoskeletal Stabilization Abdominal Expansion Training
    Dynamic Neuromusculoskeletal Stabilization abdominal expansion (DNS-AE) training focuses on coordinated breathing and abdominal expansion to facilitate intra-abdominal pressure regulation and integrated postural control. Participants receive individualized, one-on-one training delivered by licensed physical therapists, conducted twice weekly for 4 weeks. Training is performed across functional positions and task-specific movements, with instruction provided using either verbal cueing or manual f

Первичные конечные точки

  • Pain intensity [Срок оценки: At baseline, after the first week of intervention, and at the end of the 4-week intervention.]
  • Movement control performance [Срок оценки: At baseline, after the first week of intervention, and at the end of the 4-week intervention.]
Вторичные конечные точки (9)
  • Disability related to low back pain [Срок оценки: At baseline, at the end of the 4-week intervention, and at 3-month follow-up.]
  • Patient-specific functional ability [Срок оценки: At baseline, at the end of the 4-week intervention, and at 3-month follow-up.]
  • Perceived movement difficulty assessed using the Perceived Difficulty Index (PDI). [Срок оценки: At baseline, after the first week of intervention, and at the end of the 4-week intervention.]
  • Central sensitization symptoms [Срок оценки: At baseline and at the end of the 4-week intervention.]
  • Fear-avoidance beliefs [Срок оценки: At baseline and at the end of the 4-week intervention.]
  • Pain catastrophizing [Срок оценки: At baseline and at the end of the 4-week intervention.]
  • Pressure pain threshold [Срок оценки: At baseline and at the end of the 4-week intervention.]
  • Global perceived change [Срок оценки: At the end of the 4-week intervention and at 3-month follow-up.]
  • Learning acquisition during training [Срок оценки: After each training session during the 4-week intervention.]

Критерии участия

Критерии включения

  • Adults aged 18 years or older.
  • Clinically diagnosed with chronic non-specific low back pain, with symptoms persisting for more than 12 weeks.
  • Able to understand the study procedures and comply with the full intervention and assessment protocol.

Критерии исключения

  • History of surgery involving the lower back or lower extremities.
  • Presence of neurological symptoms, such as numbness or tingling sensations.
  • Signs or symptoms of nerve root compression.
  • History of any surgical procedure within the past 3 months.
  • Diagnosis of cancer.
  • Presence of major medical or psychiatric disorders.
  • Presence of systemic inflammatory disease.
  • Pregnancy.
  • Structural scoliosis of the spine.
  • Inability to ambulate or stand independently, or other conditions deemed unsuitable for participation.
  • Participation in any movement control-based exercise training within the past year.
  • Accumulated experience of more than 4 weeks of abdominal drawing-in manoeuvre (ADIM) training or Dynamic Neuromusculoskeletal Stabilization abdominal expansion (DNS-AE) training within the past year.

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

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07318454 · NYCU114229AE-S3

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗