跳至主要内容
临床试验/NCT00790517
NCT00790517已完成2 期

Reducing Weight and Diabetes Risk in an Underserved Population

Kaiser Permanente6 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2009年6月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
200
试验地点
6
主要终点
Cholesterol levels

研究概览

简要总结

The purpose of this study is to examine the effectiveness of a lifestyle intervention designed to reduce weight and diabetes risk in a population of individuals with mental illness who are also taking antipsychotic medications. We will examine the effectiveness of the intervention in

  1. reducing weight and Body Mass Index;
  2. reducing fasting insulin levels and increasing insulin sensitivity; and
  3. reducing total cholesterol and LDL cholesterol.

详细描述

Overweight and obesity are among the leading causes of preventable deaths in the US, primarily through their effects on Type II diabetes mellitus and other cardiovascular disease risk factors. Individuals with serious mental illness represent a large underserved population at greatly increased risk of obesity, diabetes, metabolic syndrome, and subsequent early mortality. These risks are amplified by the antipsychotic agents that are often prescribed to treat these mental conditions.

Although strong evidence indicates that lifestyle interventions are effective at reducing weight and other diabetes risk factors in general populations, and pilot and feasibility studies suggest that such interventions will be effective with individuals who have mental illnesses, no large-scale translational trials have examined such interventions in this population.

STRIDE is a randomized controlled trial to examine the effectiveness, in a mentally ill population, of a lifestyle intervention previously shown to be effective for reducing weight and diabetes risk factors. We target a group of individuals taking antipsychotic agents (n = 280) who receive treatment in one of two clinical settings-a publicly funded behavioral health care clinic and a non-profit private health plan. Counselors from each clinical setting will be trained in the intervention and paired with study staff to deliver it, increasing generalizability, and improving the probability of future adoption. The intervention promotes moderate calorie reduction, dietary changes, and increased energy expenditure, and is based on current clinical practice guidelines for treating obesity and cardiovascular disease.

Specific aims test the hypotheses that the intervention is more effective than usual care in: 1) reducing weight and Body Mass Index; 2) reducing fasting insulin levels and increasing insulin sensitivity; and 3) reducing total cholesterol and LDL cholesterol. A fourth aim explores effects of motivation, social support, and outcomes expectancies on primary outcomes, and moderators of intervention effectiveness (ethnicity, gender, mental illness diagnostic group, medication type, metabolic syndrome) on outcomes.

Implementation and process evaluations will assess the fidelity of intervention delivery, evaluate its acceptability; identify components participants find most and least helpful; identify barriers to, and facilitators of, lifestyle changes; and evaluate the effects of the intervention on body image, psychiatric symptoms, adherence to antipsychotic medications, quality of life, health-related self-efficacy, health, functional status, and social support. Cost-effectiveness analyses will evaluate incremental costs of producing change in each primary outcome (weight, BMI, fasting insulin levels, insulin sensitivity, and cholesterol).

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
None

入排标准

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

入选标准

  • age 18 and over
  • stable on antipsychotic agents >1 month
  • BMI in the range of 25-44.9 kg/m2
  • approved by primary care provider or psychiatrist for participation (based on mental and physical health status)
  • able and willing to provide informed consent
  • access to telephone or e-mail (for maintenance phase)

排除标准

  • children under age 18
  • diagnosis of dementia
  • psychiatrist or primary care provider indication of any medical or psychiatric contraindications for participating in a weight reduction/exercise program
  • cardiovascular event within the past 6 months (if more remote history, eligible with primary care provider or psychiatrist approval)
  • history of bariatric surgery
  • cancer diagnosis or cancer treatment in the prior 2 years (except for non-melanoma skin cancer)
  • currently pregnant or breastfeeding, or plan a pregnancy prior to the end of study participation
  • mental health hospitalization in the 30 days prior to enrollment
  • planning on moving out of the area before the 24-month follow-up assessment
  • currently enrolled in a weight-reduction program

结局指标

主要结局

Cholesterol levels

时间窗: 6, 12, 24 months

Body Mass Index

时间窗: 6, 12, 24 months

Fasting insulin levels

时间窗: 6, 12, 24 months

Weight

时间窗: 6, 12, 24 months

Insulin sensitivity

时间窗: 6, 12, 24 months

次要结局

  • Health/functional status(6, 12, 24 months)
  • Body Image(6, 12, 24 months)
  • Health-related self-efficacy(6, 12, 24 months)
  • Social support for diet/weight loss(6, 12, 24 months)
  • Antipsychotic Medication Adherence(6, 12, 24 months)
  • Psychiatric Symptoms(6, 12, 24 months)
  • Quality of life(6, 12, 24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

Loading locations...

相似试验

Reducing Weight and Diabetes Risk in an Underserved... | 临床试验