The Men on the Move Study
2018年9月19日 更新者:Dawn C. Mackey、Simon Fraser University
Shape the Path: Targeting the Health and Mobility of Older Men Through Key Community Partnerships -- The Men on the Move Study
The Men on the Move Study is a randomized, controlled, feasibility study designed to address the health problem of physical inactivity in older men.
研究概览
详细说明
Men on the Move is a randomized, controlled, feasibility study to provide preliminary evidence of feasibility and efficacy for promoting mobility through the uptake of physical activity among men aged 65 years and older who are physically inactive.
Specifically, Men on the Move will evaluate the effects of a choice-based physical activity model paired with an active transportation model.
The choice-based physical activity model encourages older men to use existing community-based resources to create and implement actions plans for physical activity.
It also provides ongoing face-to-face and telephone-based support from trained activity coaches.
The active transportation model provides transit passes and active travel planning to promote use of transit and walking to destinations of interest.
The feasibility of delivering the intervention will be assessed.
Accelerometry and travel diaries will be used to measure the effects of the intervention on physical activity.
研究类型
介入性
注册 (实际的)
58
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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British Columbia
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Vancouver、British Columbia、加拿大、V5Z1M9
- Centre for Hip Health and Mobility
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
65年 及以上 (年长者)
接受健康志愿者
是的
有资格学习的性别
男性
描述
Inclusion Criteria:
- 65 years of age and older;
- identify as a man;
- English speaking; and
- demonstrate readiness for physical activity (by the PAR-Q+ questionnaire or a letter of recommendation from their physician)
Exclusion Criteria:
- participated in any strength training in the past 3 months;
- participated in any aerobic exercise class in the past 3 months;
- live in a nursing home or assisted living facility; or
- have plans to be out of town for more than 7 days during the 12-week intervention period.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Choice-Based Physical Activity and Active Transportation
Participants will meet one-on-one with an activity coach to develop a choice-based physical activity and active transportation plan based on their interest, abilities, and resources; attend group-based motivational meetings; and receive ongoing support and encouragement for physical activity and active transportation (e.g., telephone-assisted support, community centre and transit passes).
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无干预:Wait-List Control
Participants will be offered the Choice-Based Physical Activity and Active Transportation intervention after the experimental arm has completed the study.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Feasibility of participant recruitment and retention
大体时间:12 weeks
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Number of study participants recruited and retained for the 12-week study
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12 weeks
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change from baseline in physical activity as measured by accelerometry at 12 weeks
大体时间:Baseline and 12 weeks
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Minutes/day
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Baseline and 12 weeks
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Change from baseline in daily steps as measured by accelerometry at 12 weeks
大体时间:Baseline and 12 weeks
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steps/day
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Baseline and 12 weeks
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Change from baseline in physical activity as measured by the CHAMPS questionnaire score at 12 weeks
大体时间:Baseline and 12 weeks
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Baseline and 12 weeks
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Change from baseline in active transportation as measured by travel diaries at 12 weeks
大体时间:Baseline and 12 weeks
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Trip rates (overall, by walking, by transit)
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Baseline and 12 weeks
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Change from baseline in mobility as measured by the Short Physical Performance Battery (SPPB) score at 12 weeks
大体时间:Baseline and 12 weeks
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Baseline and 12 weeks
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Change from baseline in mobility as measured by the Life-Space Assessment score at 12 weeks
大体时间:Baseline and 12 weeks
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Baseline and 12 weeks
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Heather A McKay, PhD、University of British Columbia
- 首席研究员:Joanie Sims-Gould, PhD、University of British Columbia
- 首席研究员:Meghan Winters, PhD、Simon Fraser University
- 首席研究员:Christiane Hoppmann, PhD、University of British Columbia
- 首席研究员:Alison Phinney, PhD、University of British Columbia
- 首席研究员:Karim Khan, PhD、University of British Columbia
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2015年8月1日
初级完成 (实际的)
2016年5月1日
研究完成 (实际的)
2016年5月1日
研究注册日期
首次提交
2015年7月29日
首先提交符合 QC 标准的
2015年8月17日
首次发布 (估计)
2015年8月19日
研究记录更新
最后更新发布 (实际的)
2018年9月20日
上次提交的符合 QC 标准的更新
2018年9月19日
最后验证
2018年2月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- STP-MOTM
- TE1-138295 (其他赠款/资助编号:Canadian Institutes of Health Research)
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.