Меню
Идёт набор NCT07665801

Effects of Foot Core Exercises in Patients With Total Hip Arthroplasty

Без фазы С лечением Total Hip Arthroplasty (THA)

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: Hip Rehabilitation Exercise Program, Foot-Core Exercise Program.
Кому может быть актуально
Состояния в реестре: Total Hip Arthroplasty (THA). Базовые параметры: 50 лет — 80 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
Turkey (Türkiye)
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Investigation of the Effects of Foot Core Exercises on Lower Extremity Muscle Strength, Functional Parameters, and Morphological and Viscoelastic Properties of Foot and Ankle Periarticular Structures in Patients With Total Hip Arthroplasty

Обзор

The goal of this clinical trial is to investigate the effects of foot core exercises on lower extremity muscle strength, viscoelastic properties, functional parameters, foot and ankle posture, balance, and the morphological characteristics of periarticular structures of the foot and ankle in individuals with total hip arthroplasty. The main questions it aims to answer are: * Does foot core exercises affect morphological characteristics of the periarticular structures surrounding the foot and ankle? * Does foot core exercises affect viscoelastic properties of the periarticular structures surrounding the foot and ankle? * Does foot core exercises affect lower extremity muscle strength? * Does foot core exercises affect lower extremity functional parameters and balance in individuals with total hip arthroplasty? The researchers will compare the group performing foot core exercises with the group performing routine hip exercises that do not include foot core exercises. Participitants will: * Participants will receive an exercise log after a specialist physiotherapist demonstrates the exercises in practice at the third postoperative mounth. * Visit the clinic every two months from postoperative mounth 3 to month 7 for routine follow-ups and progression of exercises. * Except for the control sessions held every two mounths, patients will be followed up through weekly phone calls. * Participants will complete an exercise diary indicating that they performed the exercises prescribed for each week, and they will bring their diaries with them to the follow-up sessions.

Вмешательства

  • Другое Hip Rehabilitation Exercise Program
    5 days per week, 40 minutes per session, for 12 weeks.
  • Другое Foot-Core Exercise Program
    5 days per week, 40 minutes per session, for 12 weeks

Первичные конечные точки

  • Ultrasonographic muscle thickness of foot and ankle periarticular structures [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Ultrasonographic cross-sectional area of foot and ankle periarticular structures [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Tone (frequency) of foot and ankle periarticular structures [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Ultrasonographic tendon morphology of foot and ankle segments [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Stiffness of foot and ankle periarticular structures [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • The damping coefficient of foot and ankle periaticular structures [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Relaxation time of foot and ankle periarticular structures [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Creep parameters of foot and ankle periarticular structures [Срок оценки: From enrollment to the end of treatment at 12 weeks]
Вторичные конечные точки (12)
  • Evaluation of lower extremity alignment [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Navicular height during weight-bearing condition [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Assessment of Hip Flexor Muscle Strength [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Assessment of Balance [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Assessment of Hip Functional Status [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Ankle Mobility Measurement [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Assessment of Foot Posture [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Assessment of Kinesiophobia [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Assessment of the Ability to Forget the Artificial Joint [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Assessment of Fear of Falling and Confidence in Avoiding Falls [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Assessment of Quality of Life [Срок оценки: From enrollment to the end of treatment at 12 weeks]
  • Navicular height during non-weight-bearing condition [Срок оценки: From enrollment to the end of treatment at 12 weeks]

Критерии участия

Критерии включения

  • Being between 50 and 80 years old,
  • Having at least 2 months elapsed since total hip arthroplasty surgery,
  • Being willing to participate in the study,
  • Being literate.

Критерии исключения

  • Having undergone revision total hip arthroplasty surgery,
  • Having a cognitive level below 21 on the MoCA scale, or having any neurological or rheumatological disease,
  • Inability to ambulate,
  • Having any history of lower extremity trauma or other surgical procedures,
  • Having toe-related pathologies that may affect pressure distribution and the course of exercise, such as hallux valgus or Morton's neuroma.

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
Тройное слепое
Основная цель
Лечение

Центры проведения

Turkey (Türkiye) · 1 центр
  • Hacettepe University — Ankara

Идентификаторы

NCT: NCT07665801 · FTREK26/20

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗