跳至主要内容
临床试验/NCT01730196
NCT01730196已完成不适用

Fit Body and Soul: A Lifestyle Intervention for Diabetes Prevention Conducted Through African American Churches

Augusta University1 个研究点 分布在 1 个国家目标入组 604 人开始时间: 2009年9月1日最近更新:
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
604
试验地点
1
主要终点
Weight change

研究概览

简要总结

Fit Body and Soul is single-blinded, cluster- randomized trial of a faith-based adaptation of the GLB program compared with a health education intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Investigator)

入排标准

年龄范围
20 Years 至 64 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Self-described African American
  • •BMI ≥25kg/m2
  • •Planning to remain within the community for 1 year
  • •Non-diabetic

排除标准

  • •Fasting plasma glucose ≥ 126 mg/dl following at least an 8-hr fast or A1C≥7.0%
  • •Active tuberculosis
  • •Cancer requiring treatment in past 5 years except for cancers that have been cured or in the opinion of the researchers has a good prognosis
  • •Stroke within the past 6 months
  • •Cirrhosis of the liver
  • •Currently pregnant or planning pregnancy within the study period
  • •Gastric weight-loss surgery
  • •Weight loss > 10% in past three months for any reason other than childbirth
  • •Anti-diabetic medications
  • •Prescription weight- loss medications
  • •Anti-neoplastic agents
  • •Anti-psychotic agents that have gluco-corticoid effect
  • •Oral corticosteroid use >6 weeks
  • •Unwilling or unable to give informed consent
  • •Unable to communicate with the church team or research group
  • •Participation in another research study that would interfere with FBAS

研究组 & 干预措施

Fit Body and Soul

Experimental

Faith-based adaptation of the Group Life Style Program

干预措施: Fit Body and Soul (Behavioral)

Wellness education

Active Comparator

A health education program developed from the list of topics provided by the Centers for Disease Control and Prevention (CDC) Guide to Community Prevention Services

干预措施: Wellness Education (Behavioral)

结局指标

主要结局

Weight change

时间窗: 12-weeks post intervention

次要结局

  • Fasting plasma glucose(12 week post intervention)
  • quality of life measures(12 week post-intervention)
  • physical activity level(12 week post-intervention)
  • cost-effectiveness(12 week post-intervetnion)
  • hemoglobin A1C(12 week intervention)

研究者

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

Richard Sattin

Professor and Research Director, Department of Emergency Medicine

Augusta University

研究点 (1)

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