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Идёт набор NCT06765486

Exercise-Induced Hypoalgesia Differences Between Upper and Lower Limbs Resistance Training Interventions

Без фазы С лечением Local Hypoalgesia Distal Hypoalgesia Resistance Training Pressure Pain Thresholds

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: Lower limb resistance training, Upper limb resistance training.
Кому может быть актуально
Состояния в реестре: Local Hypoalgesia, Distal Hypoalgesia, Resistance Training, Pressure Pain Thresholds. Базовые параметры: 18 лет — 64 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
Испания
Следующий шаг
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Официальное название

Exercise-Induced Hypoalgesia Differences at Proximal and Distal Regions After Applying a Lower Limb Resistance Training or an Upper Limb Resistance Training Protocol: A Randomized Controlled Trial in Healthy Participants

Обзор

This randomized controlled trial with healthy subjects aims to compare exercise-induced hypoalgesia among three groups: one utilizing a lower limb resistance training intervention, another using an upper limb resistance training, and a control group. The exercise protocol involves 3 sets of 5 repetitions of resistance exercises (brachial biceps curl and leg extensions). Exercise-induced hypoalgesia will be assessed by measuring pressure pain thresholds in the thigh and elbow, comparing exercise interventions with the control group. Additionally, a secondary objective is to compare the lower limb and upper limb resistance training groups in terms of their effects on pressure pain thresholds in the thigh and elbow. Thus, the study anticipates observing differences in local and distal hypoalgesia based on the trained region.

Вмешательства

  • Другое Lower limb resistance training
    Exercise intervention with leg extensions on the dominant quadriceps, doing 3 sets of 5 repetitions with the 5RM after a 5-minute warm-up with a cycle ergometer at 1 watt per kg and 60-80 revolutions per minute and 1 set of 5 repetitions with the 10RM. Previously, 72 hours before, the 5RM would have been calculated progressively approaching in sets of 5 repetitions, starting with the lower weight and stopping the test when obtaining an unsuccessful trial (the participant could not manage to lift
  • Другое Upper limb resistance training
    Exercise intervention with brachial biceps curl on the dominant brachial biceps, doing 3 sets of 5 repetitions with the 5RM after a 5-minute warm-up with a cycle ergometer at 1 watt per kg and 60-80 revolutions per minute and 1 set of 5 repetitions with the 10RM. Previously, 72 hours before, the 5RM would have been calculated progressively approaching in sets of 5 repetitions, starting with the lower weight and stopping the test when obtaining an unsuccessful trial (the participant could not man

Первичные конечные точки

  • Pain pressure threshold (PPT) on dominant quadriceps and dominant brachial biceps [Срок оценки: before, immediately after intervention, and 30 minutes after intervention.]
Вторичные конечные точки (4)
  • International Physical Activity Questionnaire (IPAQ) [Срок оценки: before intervention (up 5 minutes)]
  • Physical Activity Readiness Questionnaire (PAR-Q) [Срок оценки: before intervention (up 5 minutes)]
  • Fatigue Assessment Scale (FAS) [Срок оценки: before intervention (up 5 minutes)]
  • Rate of perceived exertion (RPE) [Срок оценки: immediately after intervention (up 10 seconds)]

Критерии участия

Критерии включения

  • Asymptomatic subjects aged between 18 and 64 years.

Критерии исключения

  • Cardiovascular, respiratory, metabolic, neurological, or osteomuscular signs or pathologies.
  • History of epilepsy.
  • Pregnant.
  • Participants who present any type of pain on the day of the measurements or who have frequently suffered pain during the previous 12 weeks.

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
Лечение

Центры проведения

Испания · 1 центр
  • CSEU LaSalle — Madrid

Идентификаторы

NCT: NCT06765486 · CSEULS-PI-013

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗