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Набира участници Не е приложимо NCT07489937

Supraspinatus Tendon Acute Effects After Two Exercise Exposures: a Crossover Randomized Trial.

Не е приложима фаза (напр. обсервационно)
Заболявания: Shoulder Pain Healthy Adult

Спонсор: University of Florida

Налично на: БГ
Обобщение
The purpose of this study is to understand acute tendon changes after two exercise programs. We will invite individuals with and without shoulder pain to participate in this study. Every individual will participate in both exercise programs separated by up to 15 days. The researcher will evaluate the shoulder tendon using ultrasound before each exercise program and at 1 hour, 6 hours and 24 hours after each exercise program. The researcher will also evaluate self reported pain, pain sensitivity testing, and self reported questionnaires. We will compare the tendon changes after each exercise program, as well as between participants with and without shoulder pain.
Кой може да участва
General inclusion criteria 1. Between 18 and 45 years of age 2. Able to perform physical activity with their shoulder (moderate arm exercise for 15 min, such as tennis or housework) General exclusion criteria 1. Shoulder fracture 2. Frozen shoulder (\>50% restriction in shoulder range of motion) 3. Shoulder surgery 4. Full rotator-cuff tears 5. Bilateral shoulder pain 6. Shoulder instability (history or positive apprehension test) 7. Corticosteroid injection in the last 6 weeks 8. Neurological diseases 9. Cardiological diseases 10. Systemic diseases (rheumatic diseases, autoimmune diseases) 11. Uncontrolled diabetes 12. Pregnancy Group-specific inclusion criteria 1. Shoulder pain group: report unilateral shoulder pain with an average shoulder pain score of≥ 3 in the last week. 2. Control group: report no shoulder pain within 6 months.
Интервенции
Isotonic exercise program
BEHAVIORAL
Plyometric exercise program
BEHAVIORAL
Места на провеждане 1
САЩ (1)
University of Florida
Gainesville , Florida
Federico Pozzi, PT, MA, PhD
Технически детайли
Статус
Набира участници
Фаза
Не е приложимо
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
45 Years
Здрави доброволци
Не
Начална дата
20.04.2026
Крайна дата
01.04.2027
Регистрационен номер
NCT07489937
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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