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Идёт набор NCT07302204

Efficacy of Aerobic Exercise Versus Therapeutic Exercises on Exercise-induced Hypoalgesia in Knee Osteoarthritis

Без фазы С лечением Osteoarthritis of the Knee

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: Aerobic Exercise, Therapeutic Exercise.
Кому может быть актуально
Состояния в реестре: Osteoarthritis of the Knee. Базовые параметры: 40 лет — 75 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
Бразилия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Efficacy of Aerobic Exercise Versus Therapeutic Exercises on Exercise-induced Hypoalgesia in Knee Osteoarthritis. Randomized Clinical Trial

Обзор

The study compares two exercise strategies in people with knee osteoarthritis. The first is aerobic exercise on a recumbent cycle ergometer, with effort controlled by the Borg scale. The second is a therapeutic exercise program with resistance, neuromuscular, mobility, and balance components. The primary objective is to determine which approach produces greater exercise induced hypoalgesia, measured by the increase in pressure pain threshold at the knee within the session across four anchor sessions during a ten week program. This is a randomized clinical trial with two parallel arms. Ninety participants, between forty five and seventy five years of age, will be allocated to one of the two groups. Allocation sequence concealment will be ensured using opaque envelopes. The outcome assessor will remain blinded to group allocation. The interventions will take place three times per week for ten weeks. Assessments will be performed at baseline and after ten weeks. Within session measurements will also be taken in weeks one, four, seven, and ten. The primary outcome is the intra session change in pressure pain threshold at the medial compartment of the knee. Secondary outcomes include exercise induced hypoalgesia in the quadriceps and trapezius, chronic adaptation of pressure pain threshold, conditioned pain modulation, pain intensity, pain self efficacy, knee related health status, functional performance, quadriceps strength, global perceived effect, and adherence. The planned sample size is forty five participants per group. The analysis will follow the intention to treat principle. The primary outcome will be compared using linear mixed models with group and time effects. Clinical outcomes at T1 will be adjusted for baseline values. Estimates, confidence intervals, and interpretation in light of minimally important differences will be reported.

Вмешательства

  • Другое Aerobic Exercise
    Supervised cycling on an electromagnetic recumbent stationary bicycle three times per week for ten weeks, with at least 24 hours between sessions.
  • Другое Therapeutic Exercise
    Individually supervised, land based therapeutic exercise program focusing on warm up, resisted strengthening, neuromuscular training, mobility and balance.

Первичные конечные точки

  • Exercise-induced hypoalgesia (EIH) [Срок оценки: At weeks 1, 4, 7, and 10 of the 10 week intervention (within session, pre and immediately post exercise).]
Вторичные конечные точки (12)
  • Exercise induced hypoalgesia of the quadriceps [Срок оценки: Within session, immediately before and immediately after the exercise session at weeks 1, 4, 7, and 10 of the 10 week intervention.]
  • Exercise induced hypoalgesia of the upper trapezius [Срок оценки: Within session, immediately before and immediately after the exercise session at weeks 1, 4, 7, and 10 of the 10 week intervention.]
  • Chronic adaptation of pressure pain threshold [Срок оценки: Baseline and after 10 weeks of intervention.]
  • Conditioned pain modulation [Срок оценки: Baseline and after 10 weeks of intervention.]
  • Pain intensity [Срок оценки: Baseline and after 10 weeks of intervention.]
  • Pain self efficacy [Срок оценки: Baseline and after 10 weeks of intervention.]
  • Knee related health status [Срок оценки: Baseline and after 10 weeks of intervention.]
  • Patient specific functional status [Срок оценки: Baseline and after 10 weeks of intervention.]
  • Functional performance, thirty second sit to stand test [Срок оценки: Baseline and after 10 weeks of intervention.]
  • Quadriceps muscle strength [Срок оценки: Baseline and after 10 weeks of intervention.]
  • Global perceived effect [Срок оценки: After 10 weeks of intervention.]
  • Adherence to the intervention [Срок оценки: Throughout the 10 week intervention period.]

Критерии участия

Критерии включения

  • Clinical diagnosis of symptomatic knee osteoarthritis for at least 3 months.
  • Report of knee pain for more than 3 months and average knee pain intensity ≥ 3 on the 0 to 10 Numeric Rating Scale.
  • Morning stiffness lasting less than 30 minutes.
  • Clinical signs compatible with knee osteoarthritis. crepitus, bony tenderness and absence of palpable warmth at the knee.
  • Altered exercise-induced hypoalgesia: absence of exercise-induced hypoalgesia and hyperalgesic response to exercise.

Критерии исключения

  • Signs and symptoms indicating the hip as the main source of pain.
  • Osteoporosis
  • Fibromyalgia
  • History of tumors or cancer
  • Active inflammatory joint diseases, such as rheumatoid arthritis or gout.
  • Previous arthroplasty of any lower limb joint.
  • Neurological diseases, including Parkinson's disease, stroke, multiple sclerosis, muscular dystrophy, motor neuron disease or Alzheimer's disease.
  • Cardiovascular diseases for which exercise is formally contraindicated.
  • Infected wounds or osteomyelitis in the knee region.
  • Deep vein thrombosis or thrombophlebitis.
  • Sensory alterations in the lower limbs.
  • Cognitive or cardiopulmonary impairments that limit safe participation in the exercise program.
  • Use of walking aids.
  • Recent knee trauma.

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

Бразилия · 2 центра
  • Cid André Fidelis de Paula Gomes — São Paulo
  • Nove de Julho University — São Paulo

Идентификаторы

NCT: NCT07302204 · 93560425.7.0000.5511

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗