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DEMOJUAN- DEMOnstration Area for Primary Prevention of Type 2 Diabetes, JUAN Mina and Barranquilla, Colombia (DEMOJUAN)

Primary Purpose

Type 2 Diabetes, Glucose Metabolism Disorders

Status
Completed
Phase
Not Applicable
Locations
Colombia
Study Type
Interventional
Intervention
Lifestyle intervention (nutrition)
Lifestyle intervention (physical activity)
Sponsored by
Centro de Investigacion Sanitaria
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Type 2 Diabetes focused on measuring impaired glucose tolerance, nutrition, physical activity

Eligibility Criteria

34 Years - 69 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 34-69 years-of-age with diagnosed IGT
  • Informed consent given.

Exclusion Criteria:

  • Patients with pharmacologically-treated diabetes
  • Hypertriglyceridaemia under drug treatment
  • History of life-limiting diseases or events
  • Unwillingness to sign the informed consent.

Sites / Locations

  • Camino Bosques de María
  • Camino Sur Occidente El Pueblo
  • Centro de INvestigacion Sanitaria
  • Paso Las Malvinas
  • Paso Nueva Era

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Lifestyle intervention (nutrition)

Lifestyle counseling (physical activity)

Arm Description

The 200 study participants of this arm will first receive 6 months of nutritional counseling and thereafter combined nutrition/physical activity counseling during 18 month. The counseling sessions consists of monthly group seminars (10 participants/group) and totally 6 individual visits with a nutritionist and 6 visits with a physical activity expert.

The 200 study participants of this arm will first receive 6 months of physical activity counseling and thereafter combined nutrition/physical activity counseling during 18 month. The counseling sessions consists of monthly group seminars (10 participants/group) and totally 6 individual visits with a nutritionist and 6 visits with a physical activity expert.

Outcomes

Primary Outcome Measures

The proportion of patients who reach normal levels of all glycaemic parameters.
Proportion of patients whose fasting glucose level is less than 6.1 mmol/l Proportion of patients whose 2-hour glucose level is less than 7.8 mmol/l

Secondary Outcome Measures

Difference in reduction of 10 year-estimated cardiovascular risk score of 10% between the standard therapy control group and the lifestyle intervention groups (WHO CVD prediction chart).
Proportion of patients whose blood pressure level is less than 130/80 mmHg Proportion of patients whose serum HDL cholesterol level is more than 1.2 mmol/l Proportion of patients whose serum LDL cholesterol level is less than 2.0 mmol/l Proportion of patients whose total/HDL cholesterol ratio is less than 4.0 Proportion of patients whose weight reduction is more than 5%

Full Information

First Posted
February 12, 2011
Last Updated
July 25, 2016
Sponsor
Centro de Investigacion Sanitaria
Collaborators
International Diabetes Federation, University of Helsinki
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1. Study Identification

Unique Protocol Identification Number
NCT01296100
Brief Title
DEMOJUAN- DEMOnstration Area for Primary Prevention of Type 2 Diabetes, JUAN Mina and Barranquilla, Colombia
Acronym
DEMOJUAN
Official Title
DEMOnstration Area for Primary Prevention of Type 2 Diabetes, JUAN Mina and Barranquilla, Colombia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
February 2011 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centro de Investigacion Sanitaria
Collaborators
International Diabetes Federation, University of Helsinki

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The main aim of this study is to investigate to what extent it is possible to reach normal glucose metabolism and optimal cardiovascular disease (CVD) risk factor levels with early lifestyle interventions in people at high risk of type 2 diabetes compared with those who receive standard therapy (usual care) only. The project will show the effect of these interventions for the first time in people of low socio-economic levels living in a Caribbean environment.
Detailed Description
Type 2 diabetes (T2D) is one of the fastest growing public health problems in both developed and developing countries. The development of T2D is a slow process and involves both genetic and environmental effects. It is commonly agreed that T2D may develop only in people that carry a genetic predisposition to the disease. Based on epidemiological observations about half of the people will develop T2D during their lifetime, and up to 30-35% will have IGT. Therefore, it is likely that more than half of the population carry genes that predispose the development of T2D. In people genetically predisposed to the disease, the probability to develop T2D is very high once exposed to unhealthy lifestyles such as obesity, unbalanced diet and physical inactivity. While we cannot change the genes, the only way to prevent T2D and its serious complications is the modification of lifestyle risk factors. Therefore, it is very important to understand the role of preventive lifestyle intervention as a key treatment in T2D prevention. Once established, T2D is difficult to treat. Despite pharmacologic treatment blood glucose levels trend to increase over time. Thus, the most efficient way to manage T2D is to prevent diabetes from developing. Also complications of T2D can best be postponed by postponing the onset of the primary disease itself. The efforts to prevent the disease need to start as early as possible and address all susceptibility factors. Fortunately, recent studies have convincingly demonstrated that prevention of T2D is possible. This project will show for the first time how lifestyle interventions work in people with IGT in the Caribbean population. The results of this study will be sued for policy making and planning of primary prevention activities not only in the local health-care system but in the entire Caribbean region.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes, Glucose Metabolism Disorders
Keywords
impaired glucose tolerance, nutrition, physical activity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
730 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lifestyle intervention (nutrition)
Arm Type
Experimental
Arm Description
The 200 study participants of this arm will first receive 6 months of nutritional counseling and thereafter combined nutrition/physical activity counseling during 18 month. The counseling sessions consists of monthly group seminars (10 participants/group) and totally 6 individual visits with a nutritionist and 6 visits with a physical activity expert.
Arm Title
Lifestyle counseling (physical activity)
Arm Type
Experimental
Arm Description
The 200 study participants of this arm will first receive 6 months of physical activity counseling and thereafter combined nutrition/physical activity counseling during 18 month. The counseling sessions consists of monthly group seminars (10 participants/group) and totally 6 individual visits with a nutritionist and 6 visits with a physical activity expert.
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle intervention (nutrition)
Intervention Description
The 200 study participants of this arm will first receive 6 months of Nutritional counseling and thereafter combined nutrition/physical activity counseling during 18 month. The counseling sessions consists of monthly group seminars (10 participants/group) and totally 6 individual visits with a nutritionist and 6 visits with a physical activity expert.
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle intervention (physical activity)
Intervention Description
The 200 study participants of this arm will first receive 6 months of physical activity counseling and thereafter combined nutrition/physical activity counseling during 18 month. The counseling sessions consists of monthly group seminars (10 participants/group) and totally 6 individual visits with a nutritionist and 6 visits with a physical activity expert.
Primary Outcome Measure Information:
Title
The proportion of patients who reach normal levels of all glycaemic parameters.
Description
Proportion of patients whose fasting glucose level is less than 6.1 mmol/l Proportion of patients whose 2-hour glucose level is less than 7.8 mmol/l
Time Frame
Month 24 of the intervention
Secondary Outcome Measure Information:
Title
Difference in reduction of 10 year-estimated cardiovascular risk score of 10% between the standard therapy control group and the lifestyle intervention groups (WHO CVD prediction chart).
Description
Proportion of patients whose blood pressure level is less than 130/80 mmHg Proportion of patients whose serum HDL cholesterol level is more than 1.2 mmol/l Proportion of patients whose serum LDL cholesterol level is less than 2.0 mmol/l Proportion of patients whose total/HDL cholesterol ratio is less than 4.0 Proportion of patients whose weight reduction is more than 5%
Time Frame
Month 24 of the intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
34 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 34-69 years-of-age with diagnosed IGT Informed consent given. Exclusion Criteria: Patients with pharmacologically-treated diabetes Hypertriglyceridaemia under drug treatment History of life-limiting diseases or events Unwillingness to sign the informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jaakko O Tuomilehto, MD, PhD
Organizational Affiliation
University of Helsinki
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tania Acosta, MD
Organizational Affiliation
CIIS LTDA
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Noël C Barengo, MD, PhD, MPH
Organizational Affiliation
CIIS LTDA
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Astrid Arrieta, MD
Organizational Affiliation
CIIS LTDA
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Carlos Ricaurte
Organizational Affiliation
CIIS LTDA
Official's Role
Study Chair
Facility Information:
Facility Name
Camino Bosques de María
City
Barranquilla
Country
Colombia
Facility Name
Camino Sur Occidente El Pueblo
City
Barranquilla
Country
Colombia
Facility Name
Centro de INvestigacion Sanitaria
City
Barranquilla
Country
Colombia
Facility Name
Paso Las Malvinas
City
Barranquilla
Country
Colombia
Facility Name
Paso Nueva Era
City
Barranquilla
Country
Colombia

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The study group is ready to share the data in de-identified format once the main results have been reported or in case any journal may ask for the data to run a check.
Citations:
PubMed Identifier
19021089
Citation
Schwarz PE, Li J, Lindstrom J, Tuomilehto J. Tools for predicting the risk of type 2 diabetes in daily practice. Horm Metab Res. 2009 Feb;41(2):86-97. doi: 10.1055/s-0028-1087203. Epub 2008 Nov 19.
Results Reference
background
PubMed Identifier
18252900
Citation
Lindstrom J, Peltonen M, Eriksson JG, Aunola S, Hamalainen H, Ilanne-Parikka P, Keinanen-Kiukaanniemi S, Uusitupa M, Tuomilehto J; Finnish Diabetes Prevention Study (DPS) Group. Determinants for the effectiveness of lifestyle intervention in the Finnish Diabetes Prevention Study. Diabetes Care. 2008 May;31(5):857-62. doi: 10.2337/dc07-2162. Epub 2008 Feb 5.
Results Reference
background
PubMed Identifier
14633807
Citation
Lindstrom J, Louheranta A, Mannelin M, Rastas M, Salminen V, Eriksson J, Uusitupa M, Tuomilehto J; Finnish Diabetes Prevention Study Group. The Finnish Diabetes Prevention Study (DPS): Lifestyle intervention and 3-year results on diet and physical activity. Diabetes Care. 2003 Dec;26(12):3230-6. doi: 10.2337/diacare.26.12.3230.
Results Reference
background
PubMed Identifier
29505512
Citation
Acosta T, Barengo NC, Arrieta A, Ricaurte C, Tuomilehto JO. A demonstration area for type 2 diabetes prevention in Barranquilla and Juan Mina (Colombia): Baseline characteristics of the study participants. Medicine (Baltimore). 2018 Jan;97(1):e9285. doi: 10.1097/MD.0000000000009285.
Results Reference
derived
Links:
URL
http://www.idfbridges.org/projects/1/4
Description
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DEMOJUAN- DEMOnstration Area for Primary Prevention of Type 2 Diabetes, JUAN Mina and Barranquilla, Colombia

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