NCT00665158已完成不适用
Prevention and Reduction of Obesity Through Active Living
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 500
- 试验地点
- 2
- 主要终点
- Waist Circumference
研究概览
简要总结
We will perform a randomized, controlled trial, the primary aim of which is to assess the effectiveness of a behavioral-based physical activity program in the prevention and treatment of obesity and related co-morbid conditions in a primary care setting. We hypothesize that the prevention and/or reduction of obesity and related co-morbidities in patients randomized to an individualized education and behavior counseling group will be greater by comparison to those randomized to a group that receives standard care alone.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 25 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Men and women between 25 and 65 years of age.
- •Sedentary lifestyle (planned physical activity for the purpose of health one day per week or less).
- •Abdominally obese (waist circumference greater than 88 and 102 cm for women and men respectively).
- •Weight stable (± 2 kg) for 6 months prior to the beginning of the study.
- •BMI between 25 and 34.9 kg/m2 (Because a lifestyle-based intervention alone for obesity reduction is ideal for persons with a BMI greater less than 35, and, that 94% of overweight and obese Canadian adults have a BMI between 25 and 34.9 kg/m2, subjects with a BMI 35 or greater will be excluded).
排除标准
- •Physical impairment which would make the intervention very difficult, or unsafe according to the patient's physician including history of myocardial infarction, stroke, coronary bypass surgery or angioplasty in the last 6 months; peripheral artery disease, unstable angina or ischemia, uncontrolled or insulin dependent diabetes mellitus.
- •Alcohol consumption > 21 drinks per week.
- •Plans to move from the area.
- •Participating in another research study.
- •Clinically judged to be unsuitable for participation or adherence
- •Inability or unwillingness to provide informed consent.
- •For women, planned pregnancy in the next 3 years.
研究组 & 干预措施
UC
Active Comparator
Usual Care Group
干预措施: UC (Usual Care Group) (Behavioral)
BI
Active Comparator
Behavioural Intervention Group
干预措施: BI (Behavioral Intervention Group) (Behavioral)
结局指标
主要结局
Waist Circumference
时间窗: 2 Years
次要结局
- Metabolic Syndrome(2 Years)
研究者
研究点 (2)
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