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临床试验/NCT04627493
NCT04627493已完成不适用

Improving Physical Activity and Mobility, During a Pandemic, Via Live Online Exercise Sessions for Older Persons: a Pilot RCT

McMaster University1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2020年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
33
试验地点
1
主要终点
Changes in physical activity

研究概览

简要总结

The COVID-19 pandemic has undoubtedly resulted in an increased level of personal anxiety, reduced access to support services, and as a secondary complication, increased physical inactivity. Older people appear to be at higher risk of several secondary complications and long-term negative health outcomes. These complications include declines in physical health and mobility, social isolation, and worsening mental health. There is strong evidence in older persons that supports the role of exercise and physical activity in: the alleviation of strength and mobility declines, reducing anxiety and depression, and alleviating cognitive declines. Exercise-based intervention trials have also been shown to reduce social isolation and loneliness. This study will compare an online exercise program delivered via Zoom and a waitlist control group in healthy older persons.

详细描述

This study will examine the impacts of an online exercise program in healthy older persons compared to a waitlist control group. Briefly, participants (healthy persons, age 65-80 years old) will participate in an online group exercise program (designed to meet Canada's Physical Activity Guidelines) via Zoom delivered by Registered Kinesiologists and Physiotherapists for a total of 8 weeks. Participants will be randomly assigned to the exercise group or the waitlist control group. Participants' will undergo assessments of physical activity, life-space mobility, nutrition, loneliness, depression, and anxiety at baseline, end of study, and 8-weeks following the end of the intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
65 Years 至 80 Years(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Exclusion Criteria:
  • Experience any physical conditions which may prevent them from engaging in moderate-intensity physical activity including using assistive walking devices (e.g. cane or walker), or injuries;
  • Have a history of neuromuscular conditions or muscle wasting diseases;
  • Are currently participating in physical activity, ≥150 minutes of moderate-to-vigorous physical activity per week;
  • Are not eligible to participate in regular physical activity according to the Canadian Society Exercise Physiology Get Active Questionnaire;
  • Do not have access to the internet at home via a personal smartphone, tablet (e.g., iPad), or computer.

排除标准

  • Experience any physical conditions which may prevent them from engaging in moderate-intensity physical activity including using assistive walking devices (e.g. cane or walker), or injuries;
  • Have a history of neuromuscular conditions or muscle wasting diseases;
  • Are currently participating in physical activity, ≥150 minutes of moderate-to-vigorous physical activity per week;
  • Are not eligible to participate in regular physical activity according to the Canadian Society Exercise Physiology Get Active Questionnaire;
  • Do not have access to the internet at home via a personal smartphone, tablet (e.g., iPad), or computer.

研究组 & 干预措施

Waitlist (Control)

No Intervention

Usual care

Exercise

Experimental

Online exercise program

干预措施: Online exercise (Behavioral)

结局指标

主要结局

Changes in physical activity

时间窗: Baseline, post intervention, 8-week follow-up

7 day steps and activity-related energy expenditure

次要结局

  • Change in the Geriatric Depression Scale score(Baseline, post intervention, 8-week follow-up)
  • Change in life-space mobility score(Baseline, post intervention, 8-week follow-up)
  • Change in feelings of loneliness(Baseline, post intervention, 8-week follow-up)
  • Participants experiences and perceptions(1-60 days post intervention)
  • Change in nutrition(Baseline, post intervention, 8-week follow-up)
  • Program Feasibility(Throughout the participant's intervention period (0-8 weeks))
  • Change in the Geriatric Anxiety Inventory score(Baseline, post intervention, 8-week follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Stuart Phillips

Professor

McMaster University

研究点 (1)

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