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临床试验/NCT03049839
NCT03049839Unknown不适用

Evaluation of a Community Health Program for the Prevention of Type 2 Diabetes and Other Cardio-metabolic Risk Factors in Adults: Districts of Barranquilla and Bogota, Colombia - January 2017 - December 2019

Universidad del Norte2 个研究点 分布在 1 个国家目标入组 650 人开始时间: 2017年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
650
试验地点
2
主要终点
Reduction of body weight average at year-end structured intervention compared with the baseline.

研究概览

简要总结

The main aim of this study is to evaluate the feasibility and effectiveness of a program for modifying lifestyles for diabetes prevention type 2 and control cardio-metabolic risk factors in adults with different categories of risk from the primary health care strategy.

The project will show the effect of these interventions for the first time in people With different risk of developing type 2 diabetes throughout the life in populations living in Colombia Located in 2 different cities, one of them in the interior of the country (districts of Bogota) and another in the north coast (districts of Barranquilla) .

详细描述

Cardiovascular disease (CVD) and type 2 diabetes (T2D) are currently the public health problems fastest growing globally. According to the International Diabetes Federation (IDF) is estimated to have diabetes approximately 382 million people in the world. It is shown that early interventions in lifestyle can reduce the burden of type 2 diabetes and factors of cardiovascular modifiable risk.

This is an intervention study in cluster. 36-month integrated into 4 phases:

  1. Design and adaptation of educational intervention
  2. Population Screening
  3. Stepwise intervention program
  4. Evaluation results.

For population screening test FINDRISC validated for the Latin American population will be employed and a score of 12 will be considered as a cutoff to all who have a score equal to or greater than 12 (moderate or high risk) they perform a test oral glucose tolerance (OGTT) according to the results 3 groups will be established

  • High risk group: Subjects with FINDRISC score ≥12 and impaired glucose tolerance (IGT)
  • Moderate risk group: Subjects with FINDRISC score ≥12 and impaired fasting glucose or norm tolerant
  • Low risk group: Subjects with FINDRISC score <12.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
30 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • People over age 30 years, residents within the perimeter of the conglomerate in the districts of Barranquilla and Bogota
  • Wishing to participate and sign informed consent

排除标准

  • DT2 known and / or treated
  • History of diseases or events that prevent their participation
  • Neurological disability that does not allow you to make own decisions
  • Pregnant women

研究组 & 干预措施

Intervention_ structured

Experimental

One year Structured intervention program for members of high-risk group (People with glucose intolerance in the OGTT and FINDRISC score ≥12 points) 10 educational group sessions where they will receive information to change lifestyle (1 per 1.5 month)

干预措施: Intervention_ S (Behavioral)

Intervention_ Informative

Experimental

Program information intervention for the group with moderate risk. One year Informative intervention program (People with normotolerant or impaired fasting glucose in the OGTT and FINDRISC score ≥12 points).

There is a single group session where they receive information to prevent cardiomatabolic risk factors

干预措施: Intervention_ I (Behavioral)

Intervention_ Communitarian

Experimental

One year, Intervention program at Community level. People with a FINDRISC less than 12 points.

Campaigns are carried out at the community level with different strategies (leaflets, booklets) to prevent cardiomatabolic risk factors

干预措施: Intervention_ C (Behavioral)

结局指标

主要结局

Reduction of body weight average at year-end structured intervention compared with the baseline.

时间窗: 12 Months

Reduction of body weight in kilograms

次要结局

  • Reduction of fasting glucose level at year-end intervention program (all groups) compared with baseline.(12 Months)
  • Reduction of 2-hour glucose level at year-end structured and informative intervention program compared with baseline.(12 Months)
  • Reduced of waist circumference average at year-end structured intervention program compared with baseline.(12 Months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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