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The Effect of Physical Activity Intervention Flexibility on the Time Course of Changes in Body Composition and Metabolism

2016年10月27日 更新者:Dr Andrew Blannin、University of Birmingham

The investigators goal is to optimise physical activity interventions to help previously inactive women improve their body shape and composition. Many people seeking to lose weight or improve body composition initiate an exercise programme. The most common recommendation of an exercise intervention for someone attempting to manage their weight, has been to 'prescribe' the recommended 150 minutes of exercise per week (World Health Organisation), often using one mode of exercise. An alternative approach might be to offer a portfolio of activities, from which the exerciser can pick and choose, to facilitate greater amounts of physical activity. The problem with this is how do you account for the different intensities of walking, washing the car, playing badminton, cycling, jogging, etc? In this study, the investigators will try to overcome this barrier by allocating a number of "physical activity points" to each activity. Using this physical activity points system, participants will be provided with a points target that they can meet using any combination of activities.

The investigators research aim is therefore to compare this points-based system against the traditional 5x30minute prescription (and sedentary control) for their ability to help previously inactive women to drop a dress size, increase fat burning, positively change their body composition and tone their tummy.

研究概览

地位

未知

干预/治疗

研究类型

介入性

注册 (预期的)

60

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

      • Birmingham、英国、B15 2TT
        • University of Birmingham, School of Sport, Exercise and Rehabilitation Sciences

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

25年 至 50年 (成人)

接受健康志愿者

不

有资格学习的性别

女性

描述

Inclusion Criteria:

  • Female
  • Aged 25-50 years old
  • Inactive (less than 150 minutes of moderate-intensity aerobic physical activity per week)
  • BMI 25-35 kg/m2
  • Good general health, as assessed by the School of Sport, Exercise and Rehabilitation Sciences' General Health Questionnaire
  • Willing to strictly comply with all study procedures and restrictions
  • Willing to participate, as demonstrated by voluntary written informed consent

Exclusion Criteria:

  • Positive result from the urine sample pregnancy test
  • Currently breast feeding
  • Currently participating in another clinical trial deemed to potentially interfere with this study
  • Current or recent (within the last 30 days) smoker
  • Currently taking prescription or non-prescription medication that may interfere with metabolism (including beta-blockers, insulin, bronchodilators, anti-inflammatory agents, thyroxine and medication/supplements that in the opinion of the investigators may affect metabolism).

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:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Prescribed exercise
Participants will be asked to choose one activity and stick to it for the duration of the intervention. Participants will be able to choose between brisk walking/slow jogging or cycling. The intervention will require the completion of 30 minutes of chosen activity on 5 days of the week, which will be recorded in a physical activity diary.
实验性的:Points-based physical activity
Participants will be asked to achieve a pre-set, individualised points target for physical activity each week. Points are acquired through the completion of a minimum 10 minutes of activity, choosing from the extensive list of activities provided; for example, 10 minutes of jogging achieves 4.5 points, whereas 10 minutes of washing a car achieves 1.5 points. The target will be 35-40 points per week, which equates to approximately 6 points per day. Any combination of activity, duration and frequency can be selected.
无干预:Waiting list control
Participants will be asked to maintain their normal activities and diet. They will be added to a waiting list to receive either exercise intervention after completing the 24-week trial period, so that they do not miss out on the opportunity to receive the exercise intervention.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Change in body composition (fat and fat-free mass in kg)
大体时间:4 weeks, 12 weeks and 24 weeks
4 weeks, 12 weeks and 24 weeks

次要结果测量

结果测量
大体时间
Perceived body shape
大体时间:4 weeks, 12 weeks and 24 weeks
4 weeks, 12 weeks and 24 weeks
Maximal aerobic capacity
大体时间:4 weeks, 12 weeks, 24 weeks
4 weeks, 12 weeks, 24 weeks
Fat oxidation rates
大体时间:4 weeks, 12 weeks and 24 weeks
4 weeks, 12 weeks and 24 weeks
Body tone
大体时间:4 weeks, 12 weeks, 24 weeks
4 weeks, 12 weeks, 24 weeks

其他结果措施

结果测量
大体时间
Blood-borne markers of metabolic health
大体时间:4 weeks, 12 weeks, 24 weeks
4 weeks, 12 weeks, 24 weeks
Psychological measures relating to perceived body image
大体时间:4 weeks, 12 weeks, 24 weeks
4 weeks, 12 weeks, 24 weeks
Psychological measures of attitudes towards exercise and physical activity
大体时间:4 weeks, 12 weeks, 24 weeks
4 weeks, 12 weeks, 24 weeks

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。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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

2013年12月1日

初级完成 (预期的)

2017年12月1日

研究完成 (预期的)

2017年12月1日

研究注册日期

首次提交

2013年12月12日

首先提交符合 QC 标准的

2013年12月18日

首次发布 (估计)

2013年12月24日

研究记录更新

最后更新发布 (估计)

2016年10月28日

上次提交的符合 QC 标准的更新

2016年10月27日

最后验证

2016年10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

  • Bham_CPW_PhysActIntervention

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

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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