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Набор скоро начнётся NCT07082504

Effects of Exercise, Cognitive Training, and Their Combination in Institutionalized Older Adults

Без фазы С лечением Aging Institutionalized Older Adults Cognitive Abilities Mobility and Independence

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: Physical Exercise Program, Cognitive Stimulation Program, Combined Physical Exercise and Cognitive Stimulation.
Кому может быть актуально
Состояния в реестре: Aging, Institutionalized Older Adults, Cognitive Abilities, Mobility and Independence. Базовые параметры: от 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
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Effects of Physical Exercise Programs, Cognitive Stimulation, and Their Combination on Mobility, Cognitive Function, and Psychosocial Well-Being in Institutionalized Older Adults

Обзор

The goal of this clinical trial is to learn if physical exercise, cognitive stimulation, or a combination of both can improve mobility, cognitive function, and psychosocial well-being in institutionalized older adults aged 65 and older. The main questions it aims to answer are: * Does physical exercise improve strength, flexibility, balance, and mobility? * Does cognitive stimulation improve executive function and mental state? * Does combining both interventions provide greater benefits than either intervention alone? Researchers will compare the physical exercise group, the cognitive stimulation group, and the combined group to a control group that receives no active intervention to see which approach leads to the most improvement. Participants will: * Take part in either physical exercise, cognitive stimulation, or both, 3 times per week for 12 weeks * Complete assessments before the intervention, after 12 weeks, and again after 6 months * Answer questionnaires and perform physical and cognitive tests to measure changes in health and well-being

Вмешательства

  • Поведенческое Physical Exercise Program
    Participants will complete supervised moderate-intensity physical exercise sessions three times per week for 12 weeks (totaling 150 minutes per week). The program includes balance, flexibility, strength, and mobility exercises designed according to WHO and ACSM guidelines for older adults. Sessions are delivered in small groups by trained physiotherapists.
  • Поведенческое Cognitive Stimulation Program
    Participants will attend cognitive stimulation sessions three times per week for 12 weeks. Activities include memory games, attention tasks, puzzles, orientation exercises, and problem-solving strategies. The sessions are led by a psychologist and a trained social educator, in small groups.
  • Поведенческое Combined Physical Exercise and Cognitive Stimulation
    Participants will receive both the physical exercise and cognitive stimulation interventions, conducted in parallel, over a 12-week period with three sessions per week. The combined program aims to improve physical and cognitive functions simultaneously and is delivered by a multidisciplinary team.

Первичные конечные точки

  • Change from Baseline in Functional Mobility Measured by the Timed Up and Go (TUG) Test at 12 Weeks [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
  • Change from Baseline in Executive Function Assessed by the Stroop Test at 12 Weeks [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
  • Change from Baseline in Quality of Life Measured by EQ-5D at 12 Weeks [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
Вторичные конечные точки (10)
  • Change in Balance Performance Measured by the Tinetti Performance Oriented Mobility Assessment (POMA) at 12 Weeks [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
  • Change in Lower Body Strength Measured by the 30-Second Chair Stand Test at 12 Weeks [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
  • Change in Upper Body Strength Measured by the Arm Curl Test at 12 Weeks [Срок оценки: From baseline to 12 weeks post-intervention.]
  • Change in Grip Strength Measured by Hand Dynamometer at 12 Weeks [Срок оценки: From baseline to 12 weeks post-intervention.]
  • Change in Sleep Quality Measured by the Pittsburgh Sleep Quality Index (PSQI) at 12 Weeks [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
  • Change in Depressive Symptoms Measured by the Geriatric Depression Scale (GDS) at 12 Weeks [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
  • Change in Life Satisfaction Measured by the Satisfaction With Life Scale (SWLS) at 12 Weeks [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
  • Change in Functional Mobility Measured by the Timed Up and Go (TUG) Test at 6-Month Follow-Up [Срок оценки: From the end of the intervention to 6 months follow-up.]
  • Change in Executive Function Measured by the Stroop Test at 6-Month Follow-Up [Срок оценки: From baseline to the end of the intervention at 12 weeks.]
  • Change in Quality of Life Measured by the EQ-5D at 6-Month Follow-Up [Срок оценки: From end of intervention to 6 months post-intervention.]

Критерии участия

Критерии включения

  • Individuals of both sexes.
  • Age 65 years or older.
  • Retired.
  • Institutionalized for more than three months.
  • Provide informed consent and agree to participate.

Критерии исключения

  • Lack of cooperation or cognitive capacity to participate.
  • Diagnosis of dementia or Alzheimer's disease.
  • Presence of acute medical conditions.
  • Physical or cognitive impairments that prevent completion of study procedures.

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

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07082504 · 1379

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗