A Novel Approach to Reducing Adiposity 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
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Virginia
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Richmond、Virginia、美国、23298
- Virginia Commonwealth University School of Medicine
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- self-identify as a man
- 18-35 years old
- BMI 25-45kg/m2
- Live in North America
Exclusion Criteria:
- an uncontrolled medical condition that might make it unsafe to change their eating or engage in unsupervised physical activity (e.g., uncontrolled hypertension)
- a diagnosis of Type 1 or Type 2 diabetes
- 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
- currently enrolled in another weight loss program, taking weight loss medication or history of weight loss surgery
- change in medication(s) within the last 3 months that could influence weight (e.g., steroids)
- have lost > 5% body weight within the last 3 months
- report a history of anorexia nervosa or bulimia nervosa or any compensatory behaviors within the previous 3 months
- report hospitalization for a psychiatric condition within the last year
- report high alcohol intake (AUDIT score > 16).
- are not able to speak and read English
- do not possess a mobile device or are unwilling to use it to receive study text messages
- 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
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 |
|---|---|
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无干预:Delayed Treatment Control group
Participants will receive the treatment after completion of the 3-month follow-up assessment
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实验性的:Lifestyle group
Participants will receive the treatment immediately
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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.
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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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Percent weight lost
大体时间:3 months
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Percent weight change (measured in kg via calibrated scale); calculated as: (post-treatment weight - baseline weight) / baseline weight *100
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3 months
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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 in perceived risk for heart disease
大体时间:Baseline to 3 months
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Perceived risk assessed via 12-item Risk Behavior Diagnosis scale
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Baseline to 3 months
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Change in minutes of moderate to vigorous physical activity
大体时间:Baseline to 3 months
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Physical activity assessed via 21-item Global Physical Activity Questionnaire
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Baseline to 3 months
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Change in diet quality
大体时间:Baseline to 3 months
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Dietary habits assessed via 26-item National Cancer Institute's Dietary Screening Questionnaire
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Baseline to 3 months
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Change in sleep quality
大体时间:Baseline to 3 months
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Sleep habits assessed via 6-item Common Elements Sleep Quesitonnaire
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Baseline to 3 months
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合作者和调查者
调查人员
- 首席研究员:Jessica G LaRose, PhD、Virginia Commonwealth University
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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.