INVESTIGATION OF THE EFFECTS OF POSTURAL EXERCISES AND TAPING
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: Exercise, kinesiotape.
- Кому может быть актуально
- Состояния в реестре: Neck Pain. Базовые параметры: 25 лет — 55 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 →
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Официальное название
INVESTIGATION OF THE EFFECTS OF POSTURAL EXERCISES AND TAPING IN OFFICE WORKERS WITH CHRONIC NECK PAIN
Обзор
The aim of this randomized controlled trial is to evaluate and compare the efficacy of Kinesio Taping (KT) and a structured exercise program on pain, disability, balance, and psychosocial well-being in desk-based office workers with chronic neck pain. Background: Prolonged sedentary work, particularly desk jobs exceeding six hours per day, is a significant risk factor for chronic neck pain and postural dysfunction. This study focuses on employees of the Kocaeli Governorate to determine which conservative intervention-active (exercise) or passive/supportive (taping)-provides superior clinical outcomes. Methods: A total of 45 volunteers (minimum 15 per group) aged 25-55, who work at desks for at least six hours a day and suffer from chronic neck pain, will be enrolled. Participants will be randomly assigned to one of three groups for a 4-week intervention period: Kinesio Taping Group: Participants will receive therapeutic taping for the cervical region. Exercise Group: Participants will undergo a structured program focusing on neck stabilization and postural correction. Control Group: Participants will receive no active intervention and will maintain their routine activities. Outcome Measures: Comprehensive assessments will be conducted at baseline and at the end of the 4-week program: Pain \& Disability: Visual Analog Scale (VAS) and Neck Disability Index (NDI). Physical Performance: Balance tests and Deep Neck Flexor Endurance test. Psychosocial Status: Quality of Life (SF-36) and depression levels (Beck Depression Inventory).
Вмешательства
- Другое Exercise
Neck and posture exercises will be given to the participants Third times a week for four weeks. - Другое kinesiotape
Neck kinesiotape will be applied by a physiotherapist
Первичные конечные точки
- Depression [Срок оценки: Baseline and at the end of treatment (Week 4)]
- Balance test [Срок оценки: Baseline and at the end of treatment (week 4)]
- Deep flexor endurance test [Срок оценки: Baseline and at the end of treatment (week 4)]
- SF 36 Quality of life [Срок оценки: Baseline and at the end of treatment (week 4)]
- Pain Assessment [Срок оценки: Baseline and at the end of treatment (week 4)]
- Disability [Срок оценки: Baseline and at the end of treatment (week 4)]
Критерии участия
Критерии включения
- Those who have had neck pain for at least 3 months, Those who have worked at a desk for at least 3 years, Those who work at a computer for at least 6 hours or more a day during working hours, Those who sign the voluntary consent form.
Критерии исключения
- Individuals who have received any physiotherapy program due to neck or back pain within the last 3 months, those with acute torticollis, those who have undergone cervical spine surgery, those with a history of fractures in the cervical vertebrae, those with conditions that will prevent evaluation or communication (such as cognitive problems), individuals with proven specific pathological conditions such as malignancy, fracture, systemic rheumatoid disease, or other musculoskeletal problems that may also affect the cervical region, such as impingement and thoracic outlet, those allergic to kinesiobands
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
Turkey (Türkiye) · 1 центр
- Istanbul Rumeli University — Istanbul
Идентификаторы
NCT: NCT07486232 · E-53938333-050-56099