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A Novel Approach to Reducing Adiposity Among Young Men

2021年7月19日 更新者:Virginia Commonwealth University
The purpose of this research study is to find out whether a primarily self-guided program can produce changes in weight, body fat and cardiovascular risk among young men.

研究概览

详细说明

This self-guided lifestyle intervention may help men to reduce weight and improve heart health because it has been adapted to meet the possible weight loss needs of young men. Young men may experience reductions in body weight after enrollment in the intervention, but this is unknown.

Study participation lasts approximately 3 months. Participants will be assessed by the study staff and fill out questionnaires about current lifestyle practices (diet, physical activity, sleep habits, risk behaviors). Weight, medical events, and medication use within the last 3 months will be assessed. Eligible participants will be randomly assigned (like the flip of a coin) to the control group or self-guided group.

研究类型

介入性

注册 (实际的)

35

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

    • Virginia
      • Richmond、Virginia、美国、23298
        • Virginia Commonwealth University School of Medicine

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 35年 (成人)

接受健康志愿者

不

有资格学习的性别

男性

描述

Inclusion Criteria:

  1. self-identify as a man
  2. 18-35 years old
  3. BMI 25-45kg/m2
  4. Live in North America

Exclusion Criteria:

  1. an uncontrolled medical condition that might make it unsafe to change their eating or engage in unsupervised physical activity (e.g., uncontrolled hypertension)
  2. a diagnosis of Type 1 or Type 2 diabetes
  3. report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q), which will be administered during prescreen
  4. currently enrolled in another weight loss program, taking weight loss medication or history of weight loss surgery
  5. change in medication(s) within the last 3 months that could influence weight (e.g., steroids)
  6. have lost > 5% body weight within the last 3 months
  7. report a history of anorexia nervosa or bulimia nervosa or any compensatory behaviors within the previous 3 months
  8. report hospitalization for a psychiatric condition within the last year
  9. report high alcohol intake (AUDIT score > 16).
  10. are not able to speak and read English
  11. do not possess a mobile device or are unwilling to use it to receive study text messages
  12. Given strict data regulations outside of North America (i.e., Europe), we will only include participants living in North America (i.e., United States, Canada).

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:双倍的

武器和干预

参与者组/臂
干预/治疗
无干预:Delayed Treatment Control group
Participants will receive the treatment after completion of the 3-month follow-up assessment
实验性的:Lifestyle group
Participants will receive the treatment immediately
The intervention will consist of one 60-minute group based online session, adapted specifically for young men based previous work with young adults, followed by a self-guided program for 12-weeks. Participants will receive a tool kit that includes evidence-based resources (scale for self-weighing, handouts that will include free self-monitoring apps and strategies for no-cost exercise, sample meal plans and meal planning tips, and tips for healthy living that emphasize risk areas) to assist them during the self-guided phase, as well as weekly health risk text messages.

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
Percent weight lost
大体时间:3 months
Percent weight change (measured in kg via calibrated scale); calculated as: (post-treatment weight - baseline weight) / baseline weight *100
3 months

次要结果测量

结果测量
措施说明
大体时间
Change in perceived risk for heart disease
大体时间:Baseline to 3 months
Perceived risk assessed via 12-item Risk Behavior Diagnosis scale
Baseline to 3 months
Change in minutes of moderate to vigorous physical activity
大体时间:Baseline to 3 months
Physical activity assessed via 21-item Global Physical Activity Questionnaire
Baseline to 3 months
Change in diet quality
大体时间:Baseline to 3 months
Dietary habits assessed via 26-item National Cancer Institute's Dietary Screening Questionnaire
Baseline to 3 months
Change in sleep quality
大体时间:Baseline to 3 months
Sleep habits assessed via 6-item Common Elements Sleep Quesitonnaire
Baseline to 3 months

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:Jessica G LaRose, PhD、Virginia Commonwealth University

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)

2021年1月20日

初级完成 (实际的)

2021年7月1日

研究完成 (实际的)

2021年7月1日

研究注册日期

首次提交

2020年2月10日

首先提交符合 QC 标准的

2020年2月10日

首次发布 (实际的)

2020年2月12日

研究记录更新

最后更新发布 (实际的)

2021年7月26日

上次提交的符合 QC 标准的更新

2021年7月19日

最后验证

2021年7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

  • HM20015458

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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

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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