跳至主要内容
临床试验/NCT00119795
NCT00119795已完成不适用

Cooperative Lifestyle Intervention Program (CLIP)

Wake Forest University Health Sciences6 个研究点 分布在 1 个国家目标入组 288 人开始时间: 2005年8月最近更新:
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
288
试验地点
6
主要终点
400 meter walk

研究概览

简要总结

To test the effects of exercise and weight loss on mobility disability of older overweight/obese men and women who have evidence of cardiovascular disease or the metabolic syndrome.

详细描述

BACKGROUND:

Older adults make up the fastest growing segment of our population. It is estimated that by the year 2030, elderly people will make up 22% of the United States population. A large portion of older adults suffers from one or more chronic conditions that could be improved by regular physical activity. Therefore, research in this age group is needed.

DESIGN NARRATIVE:

The Cooperative Lifestyle Intervention Program (CLIP) will test the effects of a physical activity intervention and a weight loss intervention on mobility disability of overweight or obese men and women who have evidence of cardiovascular disease or the metabolic syndrome. The public health relevance of the trial lies in the fact that the interventions will be delivered in conjunction with four Cooperative Extension Centers in counties surrounding Winston-Salem, North Carolina. CLIP will be designed as a three arm, randomized, controlled trial. The three 18-month treatments will include: (1) a basic health education-based control condition, (2) a group treatment program for physical activity, and (3) a lifestyle intervention designed to reduce sedentary behavior and promote weight loss. The primary aim will be to compare the effects of the three treatment arms on the change in performance on a 400-meter walk test over the course of 18 months. Secondary aims will include changes in cardiovascular risk factors, adiposity, cardiovascular fitness, physical activity, and health-related quality of life. Analyses will also be conducted to determine whether changes in the primary outcome are mediated by changes in constructs from social cognitive theory.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
60 Years 至 79 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Currently living in one of the counties surrounding Winston-Salem, NC
  • Sedentary (engages in fewer than 30 minutes of moderate structured physical activity for at least 10 minutes at a time each week)
  • Overweight or obese, as defined by a body mass index (BMI) greater than 25
  • Fasting glucose level less than 140
  • Documented evidence of an MI, PCTA, chronic stable angina, or cardiovascular surgery (coronary artery or valvular heart disease) within the 6 months prior to study entry or an ATP III diagnosis of the metabolic syndrome
  • Disability defined as self-reported difficulty with walking ¼ mile, climbing stairs, lifting and carrying groceries, or performing other household chores such as cleaning and yard work
  • Does not plan to move out of the county of residence for the duration of the study

排除标准

  • Diagnosis of bipolar depression or schizophrenia (defined as self-reported treatment for these conditions)
  • Currently receiving lithium or neuroleptics
  • Evidence of unstable angina, symptomatic congestive heart failure, or exercise-induced complex ventricular arrhythmias
  • Resting blood pressure greater than 160/100 mmHg
  • Diagnosis of any of the following: Parkinson's disease; chronic liver disease (cirrhosis, chronic hepatitis, etc.); systemic rheumatic condition (rheumatoid arthritis, psoriatic arthritis, Reiter's disease, systemic lupus erythematosus, etc.); end stage renal disease; or other systemic diseases or abnormal laboratory values which would preclude participants from safely participating in the protocol or impair their ability to complete the study
  • Actively being treated for cancer (other than non-melanotic skin cancer)
  • Significant visual or hearing impairment that cannot be corrected and results in the inability to use the telephone or hear normal conversation
  • Currently participating in or planning to participate in another medical intervention study
  • Current alcohol abuse disorder or consumes more than 21 alcoholic drinks per week
  • Unable to walk without assistance
  • Unable to speak or read English
  • Judged by the clinic staff to be unsuitable for the trial for any reason

研究组 & 干预措施

Health education control

Active Comparator

This is an education program for older adults entitles, successful aging.

干预措施: Health Education Control (Behavioral)

Exercise Only

Experimental

Structured exercise 150 min/wk

干预措施: Exercise (Behavioral)

Weight Loss

Experimental

Behavioral weight loss; goal of 7%

干预措施: Weight Loss (Behavioral)

结局指标

主要结局

400 meter walk

时间窗: Measured at 18 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

Loading locations...

相似试验