Periodization-Based Strength Exercise Training in İndividuals With Type 2 Diabetes
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: Non-linear Periodization-Based Strength Training, Linear Periodization-Based Strength Training, Usual Care.
- Кому может быть актуально
- Состояния в реестре: Type 2 Diabetes. Базовые параметры: 18 лет — 65 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
A Comparison of the Effects of Different Periodization-Based Strength Training Programs in Individuals With Type 2 Diabetes Mellitus
Обзор
This randomized controlled study aims to compare the effects of different periodization-based strength training approaches in individuals with type 2 diabetes mellitus. Participants will be allocated to non-linear periodization, linear periodization, or control groups. The intervention program will be conducted for 8 weeks and will evaluate exercise capacity, muscle strength, quality of life, body composition, and metabolic parameters.
Подробное описание
Type 2 diabetes mellitus is associated with reduced exercise capacity, decreased muscle strength, impaired quality of life, and metabolic dysfunction. Exercise training is recommended as an important component of diabetes management; however, the comparative effectiveness of different strength training periodization approaches remains unclear.
This randomized controlled trial aims to compare the effects of non-linear periodization and linear periodization strength training programs in individuals with type 2 diabetes mellitus. Participants will be randomized into three groups: a non-linear periodization training group, a linear periodization training group, and a control group receiving usual care.
The intervention will be conducted for 8 weeks, three times per week. Outcomes including exercise capacity, muscle strength, body composition, quality of life, and metabolic parameters will be evaluated before and after the intervention period.
Вмешательства
- Поведенческое Non-linear Periodization-Based Strength Training
Participants will perform supervised non-linear periodization-based strength training three times per week for 8 weeks. - Поведенческое Linear Periodization-Based Strength Training
Participants will perform supervised linear periodization-based strength training three times per week for 8 weeks. - Другое Usual Care
Participants will receive usual care and no structured exercise intervention during the study period.
Первичные конечные точки
- Exercise Capacity [Срок оценки: Baseline and after 8 week]
Вторичные конечные точки (8)
- Change in Peripheral Muscle Strength [Срок оценки: Baseline and after 8 weeks]
- Change in Hand Grip Strength [Срок оценки: Baseline and after 8 weeks]
- Change in Diabetes Quality of Life Questionnaire Score [Срок оценки: Baseline and after 8 weeks]
- Change in Body Fat Percentage [Срок оценки: Baseline and after 8 weeks]
- Change in Skeletal Muscle Mass [Срок оценки: Baseline and after 8 weeks]
- Change in Resting Metabolic Rate [Срок оценки: Baseline and after 8 weeks]
- Change in Hemoglobin A1c (HbA1c) [Срок оценки: Baseline and after 8 weeks]
- Change in Fasting Blood Glucose [Срок оценки: Baseline and after 8 weeks]
Критерии участия
Критерии включения
- Adults aged between 18 to 65 years
- Diagnosis of Type 2 Diabetes Mellitus (T2DM)
- Not having participated in any structured exercise program within the last 6 months
- Willingness to participate in the study and provide written informed consent
Критерии исключения
- Presence of nephropathy, retinopathy, or peripheral neuropathy
- Presence of neurological, cognitive, or orthopedic disorders that may affect outcome measurements
- Severe respiratory disease (Forced Expiratory Volume in the first second \[FEV1\] <35% or Forced Vital Capacity \[FVC\] <50%)
- Presence of ischemic heart disease or peripheral arterial disease
- History of any cardiovascular event within the last 6 months
- Current malignancy
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
- Открытое
- Основная цель
- Лечение
Центры проведения
Turkey (Türkiye) · 1 центр
- Baskent University Hospital — Ankara
Идентификаторы
NCT: NCT07659925 · T2DM-NLP-2026