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Идёт набор NCT07293702

IASTM Effects on Pain, Functionality, and Proprioception in Subacromial Impingement

Без фазы С лечением Subacromial Impingement Syndrome Massage Instrument-Assisted Soft Tissue Mobilization Soft Tissue Injuries

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: Conventional exercise group, IASTM group.
Кому может быть актуально
Состояния в реестре: Subacromial Impingement Syndrome, Massage, Instrument-Assisted Soft Tissue Mobilization, Soft Tissue Injuries. Базовые параметры: 40 лет — 60 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

**Effect of Instrument-Assisted Soft Tissue Mobilization on Pain, Functionality, and Proprioception in Individuals With Subacromial Impingement Syndrome**

Обзор

The aim of this study will be to investigate the effects of Instrument-Assisted Soft Tissue Mobilization (IASTM), applied in addition to a conventional exercise program, on pain, range of motion, proprioception, functionality, and quality of life in individuals with Subacromial Impingement Syndrome (SIS).

Подробное описание

The aim of this study will be to investigate the effects of Instrument-Assisted Soft Tissue Mobilization (IASTM), applied in addition to a conventional exercise program, on pain, range of motion, proprioception, functionality, and quality of life in individuals with Subacromial Impingement Syndrome (SIS).

A total of 38 participants will be included in the study and will be randomly assigned to either the Conventional Exercise Group or the IASTM Group. Both groups will receive treatment for 4 weeks, three sessions per week, for a total of 12 sessions.

Before the intervention, both groups will be assessed for pain (VAS), range of motion (goniometer), joint position sense (goniometer), functionality (Disabilities of the Arm, Shoulder and Hand - DASH), and quality of life (Rotator Cuff Quality of Life - RC-QoL).

Вмешательства

  • Другое Conventional exercise group
    All participants will receive a standardized electrotherapy program in a clinical setting, consisting of TENS (100 Hz, 30 minutes), ultrasound (1.5 W/cm², 8 minutes), and a 15-minute cold-pack application, delivered three times per week for four weeks. In addition to electrotherapy, participants in the conventional exercise group will perform a physiotherapist-guided exercise program aimed at improving shoulder flexion, abduction, internal and external rotation through stretching and range-of-mo
  • Другое IASTM group
    Participants in the IASTM group will receive Instrument-Assisted Soft Tissue Mobilization in addition to the conventional treatment program, three days per week for four weeks, for a total of 12 sessions. The IASTM technique will be applied to the subscapularis, anterior deltoid, biceps brachii, upper trapezius, supraspinatus, infraspinatus, teres major, teres minor, and posterior deltoid muscles. For each muscle group, the treatment will be administered for 20 seconds in a parallel direction a

Первичные конечные точки

  • Visual Analog Scale [Срок оценки: From enrollment to the end of treatment at 4 weeks]
  • Range of motion [Срок оценки: From enrollment to the end of treatment at 4 weeks]
  • The Disabilities of the Arm, Shoulder and Hand (DASH) [Срок оценки: From enrollment to the end of treatment at 4 weeks]
Вторичные конечные точки (2)
  • Joint position sense [Срок оценки: From enrollment to the end of treatment at 4 weeks]
  • Rotator cuff quality of life Index [Срок оценки: From enrollment to the end of treatment at 4 weeks]

Критерии участия

Критерии включения

  • Individuals diagnosed with SIS by MRI
  • Men and women between 40 and 60 years of age
  • Individuals with symptoms persisting for at least one month
  • Individuals with a minimum of 60° of shoulder flexion and abduction range of motion

Критерии исключения

  • Individuals with a history of surgery on the affected arm
  • Individuals with an open wound on the arm
  • Individuals with an active infection
  • Individuals with inflammatory joint disease
  • Individuals with malignant or benign tumors were excluded from the study.

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

Turkey (Türkiye) · 1 центр
  • Istanbul Medipol University — Istanbul

Идентификаторы

NCT: NCT07293702 · E-10840098-202.3.02-6969

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗