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Strategies to Enhance the Experience of Exercise

2018年10月10日 更新者:University of Colorado, Boulder
This study aims to test the effect of three cognitive strategies to affect individuals' subjective experience of cardiovascular exercise. Participants will be randomly assigned to one of three strategies to use while exercising, both during an in-person session and self-directed two week exercise period.

研究概览

研究类型

介入性

注册 (实际的)

78

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

    • Colorado
      • Boulder、Colorado、美国、80301
        • Center for Innovation and Creativity (CINC)

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

18年 至 40年 (成人)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Between the ages of 18 and 40.
  2. Insufficiently physically active for the past 6-months (i.e., does not meet American College of Sports Medicine [ACSM] guideline for cardiorespiratory exercise). The ACSM guidelines state that all healthy adults should engage in a minimum of 150 minutes per week of moderate intensity cardiorespiratory exercise, or 75 minutes per week of vigorous intensity exercise, or an equivalent combination of the two). On the eligibility screen assessment, we will define moderate and vigorous intensity exercise. Then we will ask individuals to report how many minutes of moderate and vigorous intensity exercise they engage in per week. We will use the ACSM's rule of thumb that 1 minute of moderate intensity exercise is equivalent to 2 minutes of vigorous intensity exercise. This will help to ensure that prospective participants who exercise for less than 150 minutes per week are not actually meeting the ACSM guidelines for cardiorespiratory fitness by engaging in vigorous intensity exercise. Thus, if total minutes of moderate intensity exercise and total minutes of vigorous intensity exercise (multiplied by 2) per week is equal to or greater than 150, callers will not be eligible for study inclusion.
  3. Physically capable of safely engaging in moderate-intensity physical activity (PA)
  4. Able and willing to access the Internet daily for two weeks
  5. Willing to accept random assignment.
  6. Have a smartphone or other mobile device (e.g., iPod Touch) that can play media (important if participants are assigned to the distraction condition)
  7. Willing to engage in an exercise intervention specifically involving walking, jogging, running, or hiking (not other types of exercise)

Exclusion Criteria:

  1. Are diabetic or receiving treatment for a metabolic disorder
  2. Are currently pregnant
  3. Are currently on antipsychotic medications
  4. Have a history of cardiac or respiratory disease
  5. Are receiving treatment for a heart condition or high blood pressure
  6. Experience chest pains during and/or not during physical activity
  7. Have a muscle, bone, or joint problem or injury that limit movement, make exercise painful, or could be made worse by exercising
  8. Have a close family history of an adverse cardiac event before the age of 50.

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:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:Mindfulness
Participants will use the strategy of mindfulness, i.e., present moment awareness with nonjudgment and acceptance, while exercising.
Participants will use mindfulness techniques while exercising
实验性的:Distraction
Participants will use the strategy of distraction, i.e., directing their attention to something other than exercise (specifically a podcast) while exercising.
Participants will distract themselves while exercising
有源比较器:Self-Monitoring
Participants will monitor their internal experience while exercising, without distraction and without being taught mindfulness skills of nonjudgment and acceptance.
Participants will use associative attentional focus while exercising

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
Affective valence
大体时间:30 minutes
Affective valence during a 30-minute exercise bout
30 minutes
Felt arousal
大体时间:30 minutes
Felt arousal during a 30-minute exercise bout
30 minutes
Perceived Exertion (RPE)
大体时间:30 minutes
Rating of Perceived Exertion during a 30-minute exercise bout
30 minutes
Minutes of exercise
大体时间:2-weeks following initial visit
Minutes exercised during 2-week at-home intervention
2-weeks following initial visit
Affect and perceived exertion: longitudinal
大体时间:2-weeks following initial visit
Rated affect and perceived exertion during 2-week at-home intervention
2-weeks following initial visit

次要结果测量

结果测量
措施说明
大体时间
Theory of Planned Behavior: attitudes
大体时间:Baseline to 2-week follow-up
attitudes about exercise behavior
Baseline to 2-week follow-up
Theory of Planned Behavior: norms
大体时间:Baseline to 2-week follow-up
subjective norms regarding exercise behavior
Baseline to 2-week follow-up
Theory of Planned Behavior: self-efficacy
大体时间:Baseline to 2-week follow-up
self-efficacy for exercise
Baseline to 2-week follow-up
Theory of Planned Behavior Constructs
大体时间:Baseline to 2-week follow-up
intentions to engage in future exercise behavior
Baseline to 2-week follow-up
Distress tolerance
大体时间:Baseline to 2-week follow-up
Rated ability to tolerate distress
Baseline to 2-week follow-up
Defusion skills
大体时间:Baseline to 2-week follow-up
rated ability to "defuse"
Baseline to 2-week follow-up

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。

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 (实际的)

2017年12月15日

初级完成 (实际的)

2018年8月31日

研究完成 (实际的)

2018年8月31日

研究注册日期

首次提交

2017年12月6日

首先提交符合 QC 标准的

2018年2月26日

首次发布 (实际的)

2018年3月5日

研究记录更新

最后更新发布 (实际的)

2018年10月12日

上次提交的符合 QC 标准的更新

2018年10月10日

最后验证

2018年10月1日

更多信息

与本研究相关的术语

其他研究编号

  • 17-0474

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

在美国制造并从美国出口的产品

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.

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