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Идёт набор NCT07499973

Influence of Abdominal Muscle Function on Knee Stability for Injury Prevention

Без фазы С лечением Core Strength Knee Stability

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: Core Stabilization Training Program.
Кому может быть актуально
Состояния в реестре: Core Strength, Knee Stability. Базовые параметры: 18 лет — 35 лет · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Испания
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Investigation of Core Neuromuscular Performance as a Determinant of Knee Stability and Injury Prevention in Young Female Athletes Using Vicon 3D Motion Capture and Functional Performance Tests

Обзор

The goal of this clinical trial is to learn whether an 8-week core stabilization training program can improve abdominal strength and knee stability in physically active women aged 18 to 35. The main questions it aims to answer are: Does core stabilization training improve abdominal endurance as measured by the Prone Bridge Test? Does this training enhance knee stability as measured by the Lateral Squat Down, Y-Balance Test, and Drop Vertical Jump? Researchers will compare participants' results before and after the intervention to see whether the training program leads to measurable improvements in strength and stability. Participants will: Complete baseline testing of abdominal strength and knee stability using standardized assessments (Prone Bridge Test, Lateral Squat Down, Y-Balance Test, Drop Vertical Jump) recorded with a Vicon motion-capture system. Perform an 8-week supervised core stabilization program that includes front plank, side plank, and Nordic hamstring exercises following a structured progression. Complete the same performance tests again after the intervention.

Вмешательства

  • Поведенческое Core Stabilization Training Program
    Participants will perform the following exercises for 8 weeks: Front plank: 2 × 30 seconds (with progression including alternating leg lifts) Side plank: 2 × 30 seconds per side (with progression including hip abduction) Nordic hamstring exercise: 2 sets of 3-15 repetitions depending on progression Rest between sets: 30-60 seconds based on perceived exertion. All exercises are performed under supervision prior to regular training sessions.

Первичные конечные точки

  • Change in abdominal endurance (Prone Bridge Test) [Срок оценки: Baseline and 8 weeks (post-intervention)]
Вторичные конечные точки (4)
  • Change in dynamic balance (Y-Balance Test composite score) [Срок оценки: Baseline and 8 weeks (post-intervention)]
  • Change in knee control during Lateral Squat Down (knee valgus angle) [Срок оценки: Baseline and 8 weeks (post-intervention)]
  • Change in landing mechanics (Drop Vertical Jump knee valgus angle) [Срок оценки: Baseline and 8 weeks (post-intervention)]
  • Adherence to the core training program [Срок оценки: At the end 8-week intervention]

Критерии участия

Критерии включения

  • Female participants
  • Age between 18 and 35 years
  • Performing regular physical activity ≥ 6 hours per week.
  • Able to complete all assessment procedures (Prone Bridge Test, Lateral Squat Down, Y-Balance Test, Drop Vertical Jump).
  • Willing to comply with the 8-week study procedures (training program or control condition)

Критерии исключения

  • Current musculoskeletal injury affecting the lower limbs, trunk, or spine
  • History of surgery in the lower limbs or spine in the past 12 months
  • Known neurological, cardiovascular, or systemic conditions that may interfere with physical testing
  • Pregnancy
  • Participation in any structured core-strengthening program during the study period
  • Inability to abstain from core training if assigned to the control group

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Профилактика

Центры проведения

Испания · 1 центр
  • Universidad Europea de Madrid — Villaviciosa de Odón

Идентификаторы

NCT: NCT07499973 · UEM-2026-COREKNEE-01

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗