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临床试验/NCT00129792
NCT00129792已完成不适用

Expectancy, Self-Efficacy and Outcomes in Metabolic Syndrome

Oregon Health and Science University1 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2005年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
79
试验地点
1
主要终点
Cholesterol

研究概览

简要总结

This study will determine the effects of a supplement in reducing symptoms of metabolic syndrome, a collection of symptoms that increase the risk for developing heart disease, stroke, and diabetes.

详细描述

Metabolic syndrome is a serious condition involving abnormal glucose and lipid metabolism and obesity; these symptoms are associated with a two- to fourfold increased risk for cardiovascular disease and diabetes. The dietary supplement being investigated in this study is a natural product designed to reduce metabolic syndrome by decreasing hunger, increasing energy, and improving insulin function.

This study will last 12 weeks. Participants will be randomly assigned to one of three arms. Participants in Arm 1 will receive the supplement; participants in Arm 2 will have a 50% chance of receiving either the supplement or placebo; participants in Arm 3 will receive placebo. Participants will take their assigned pills 3 times daily for 12 weeks. A follow-up visit will occur at the end of the 12 weeks; there will be a debriefing visit shortly after the follow-up visit. Participants in all 3 arms will receive weekly education and counseling sessions on healthy lifestyle changes to encourage weight loss. Blood collection will occur at study start and at the end of 12 weeks for assessment of fasting blood glucose, insulin, cholesterol, and levels of certain hormones. Participants will also be asked to complete questionnaires at study entry and at Week 12; the questionnaires will assess depression, stress, self-absorption, optimism, food cravings, hunger, the degree to which participants seek pleasure from activities, and participants' thoughts about their ability to make behavioral changes.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Body mass index (BMI) between 30 and 45
  • Live in the Portland, Oregon metropolitan area
  • Willing and able to complete a 12-week weight loss program
  • Meet at least 3 of the following 5 criteria: 1) waist circumference greater than 40 inches for men and 35 inches for women; 2) fasting triglycerides higher than 150 mg/dl; 3) high density lipoprotein (HDL) lower than 40 mg/dl for men and 50 mg/dl for women; 4) systolic blood pressure (BP) of 130 mmHg or higher or diastolic BP of 85 mmHg or higher; 5) fasting glucose of 100 mg/dl or higher

排除标准

  • Any medications, including dietary supplements, that could interfere with the study
  • Medical conditions contraindicating a diet and exercise weight loss program
  • History of congestive heart failure, stroke, myocardial infarction, coronary artery bypass graft, or atherosclerotic cardiovascular disease
  • Current diagnosis of cancer
  • Hospitalization for a psychiatric condition within 12 months prior to study entry
  • Weight loss medications within 6 months prior to study entry
  • Change in body weight greater than 5% within 6 months prior to study entry
  • Consumption of more than 21 alcoholic drinks per week
  • Current participation in another clinical trial OR living in the same household with another participant in this study
  • Currently exercising for more than 30 minutes, 3 times per week
  • Fasting blood glucose higher than 125 mg/dl
  • BP higher than 145/90
  • Triglycerides higher than 500 mg/dl
  • Training as a health care provider or health scientist
  • Pregnancy or breastfeeding

研究组 & 干预措施

3

Other

Has 0% expectation of receiving supplement.

干预措施: Education and counseling for weight loss (Behavioral)

1

Experimental

Has 100% expectation of receiving supplement

干预措施: Dietary supplement for weight loss (Drug)

1

Experimental

Has 100% expectation of receiving supplement

干预措施: Education and counseling for weight loss (Behavioral)

2

Sham Comparator

Has 50% expectation of receiving supplement

干预措施: Dietary supplement for weight loss (Drug)

2

Sham Comparator

Has 50% expectation of receiving supplement

干预措施: Education and counseling for weight loss (Behavioral)

结局指标

主要结局

Cholesterol

时间窗: baseline (Week 1) and outcome (Week 12)

weight loss

时间窗: baseline (Week 1) and outcome (Week 12)

insulin function

时间窗: baseline (Week 1) and outcome (Week 12)

次要结局

  • Cortisol levels(baseline (Week 1) and outcome (Week 12))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Barry S. Oken

MD

Oregon Health and Science University

研究点 (1)

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