Меню
Набор скоро начнётся NCT06952166

Understanding the Psychological Benefits and Neurophysiological Mechanisms of Qigong in Older Adults

Без фазы С лечением Qigong

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: Qigong (Baduanjin), Mindfulness-based intervention, Physical exercise.
Кому может быть актуально
Состояния в реестре: Qigong. Базовые параметры: от 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
Гонконг
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

One goal of the study is to evaluate the efficacy of qigong to alleviate depressive symptoms and enhance cognitive function in comparison to mindfulness-based intervention, physical exercise, and waitlist control. The other goal is to explore the changes in neurobiological markers that may explain the qigong-related effects on depressive symptoms and cognitive function. The main research questions are: * Is the 12-week qigong training more effective than mindfulness-based intervention, physical exercise, and waitlist control to alleviate depressive symptoms? * Is the 12-week qigong training more effective than mindfulness-based intervention, physical exercise, and waitlist control to enhance cognitive function? Participants are older adults aged 60 or above. They were randomly assigned to qigong training, mindfulness training, physical exercise training, or wait-list which all last for 12 weeks. Their changes before and after the 12-week period in depressive symptoms, neurobiological markers, and cognitive functions are assessed.

Вмешательства

  • Поведенческое Qigong (Baduanjin)
    Participants will receive 24 sessions of Baduanjin training over 12 weeks (2 sessions per week). Each session will last for 60 minutes. Baduanjin consists of eight forms of gentle movements, and it takes about 10 to 15 minutes to complete a full cycle. Participants will learn to practice each form gradually over the first 12 sessions. In the remaining 12 sessions, the participants will go through all the movements 2-3 times, with guided practice on rhythmic breathing and mind regulation (attenti
  • Поведенческое Mindfulness-based intervention
    Participants will receive mindfulness-based intervention with the same duration and frequency as qigong group. The intervention incorporates psychoeducation on mindfulness and stress management and group-based mindfulness practice about breathing, awareness of body sensations, thoughts, stretching, and walking. All the mindfulness practices are based on publicly accessible audio recordings. The training will be delivered by an instructor after training by the project team.
  • Поведенческое Physical exercise
    Participants of the physical exercise group will receive training of a series of low-to-moderate intensity physical activities for the same duration and frequency as qigong group. The physical activities include stretching, flexibility exercise, balance exercise, and aerobic exercise. The training will be delivered by an instructor after training by the project team.

Первичные конечные точки

  • Depressive symptoms [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • Global cognitive function [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
Вторичные конечные точки (10)
  • Serum adiponectin [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • Serum BDNF [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • Salivary cortisol [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • Attention [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • Inhibitory control [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • Working memory [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • ERP N2 amplitude [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • ERP P3 amplitude [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • Hand grip strength [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]
  • Affect [Срок оценки: Baseline and post-intervention (12 weeks after baseline)]

Критерии участия

Критерии включения

  • 60 years or older;
  • With mild or severer levels of depressive symptoms as indicated by the Geriatric Depression Scale (GDS-8) scores of 5 or above, or Depression Anxiety and Stress Scale-21 (DASS-21) depression subscale scores of 4 or above
  • Self-identified as physically stable and without life-threatening diseases.
  • Be able to communicate in Cantonese or Mandarin.

Критерии исключения

  • Have a history of practicing or receiving training of any form of mind-body or regular exercises (including tai chi, yoga, and qigong, or regular physical activity > 3 times/week) during the month prior to intervention
  • Have changed medications or the dose of medications prescribed for their health condition in the one month prior to study enrollment
  • Have severe cognitive or language impairment based on the assessment with Montreal Cognitive Assessment (MoCA)
  • Taking medication or undergoing electroconvulsive therapy, psychotherapy, or psychoeducation for a psychological or psychiatric condition
  • Unable to demonstrate satisfactory standing balance

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
Поддерживающая терапия

Центры проведения

Гонконг · 1 центр
  • Hong Kong Polytechnic University, Department of Rehabilitation Sciences — Kowloon

Идентификаторы

NCT: NCT06952166 · 15104721-2

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗