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Multifactorial Intervention in Type 2 Diabetes - Italy (MINDIT)

Primary Purpose

Type 2 Diabetes

Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Intensive care
Sponsored by
University of Parma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Type 2 Diabetes focused on measuring diabetes,, cardiovascular, risk factor, cardiovascular event, intervention

Eligibility Criteria

50 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Both genders
  • age 50-70 years
  • Type two diabetes with at least two-year history of disease and without insulin treatment in the first two years after diagnosis
  • Negative medical history for documented previous cardiovascular events or macrovascular complications
  • Written consent to participate
  • Presence of at least 2 of the following risk factors:

    • LDL cholesterol > 130 mg/dL (regardless of treatment)
    • Triglycerides > 200 mg/dL
    • HDL cholesterol < 35 (males) or 45 (females) mg/dL
    • Blood pressure > 140/90 mmHg
    • Cigarette smoking

Exclusion Criteria:

  • Age below 50 or above 70 years
  • Type 1 diabetes, diagnosis before 40 years of age, known presence of auto-antibodies or insulin requirement in the first 2 years of disease.
  • Chronic kidney failure (plasma creatinine > 2 mg/dL)
  • Significant liver damage (AST and/or ALT > 2 times the upper limits of normality)
  • History of previous cardiovascular events
  • Active neoplasms or any concomitant disease limiting life expectancy

Sites / Locations

  • Francesco Giorgino
  • Maria Dolci
  • Lamberto De Giorgio
  • Giuseppe Derosa
  • PierPaolo DeFeo
  • Donatella Zavaroni
  • Roberto Miccoli
  • Giovanni Ghirlanda
  • Mariela Trovati

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Usual Care

Intensive Care

Arm Description

Clinical practice in type 2 diabetes treatment

Intensive multi-factorial treat-to-target intervention, according to international guidelines, that includes both lifestyle intervention and a step-wise strategy for pharmacological treatment with a treat-to-target approach.

Outcomes

Primary Outcome Measures

Cardiovascular events
To verify if an intensive care intervention compared to usual care is able to significantly decrease the incidence of first cardiovascular event. Composite primary end-point = mortality for cardiovascular causes, proven acute myocardial infarction (STEMI or NSTEMI), acute coronary syndrome requiring hospitalization, proven ischemic stroke, coronary or carotid revascularization procedure

Secondary Outcome Measures

cardiovascular risk factors changes
To assess whether the intensive treatment is able to significantly improve cardiovascular risk factors with increased multiple-target achievement. A pre-planned interim analysis after two years of follow-up was foreseen by the study protocol. To verify that the intesive protocol implemented on the basis of national and international guidelines is actually feasible in a real world clinical setting.

Full Information

First Posted
November 12, 2010
Last Updated
August 11, 2011
Sponsor
University of Parma
Collaborators
Italian Society of Diabetology, AstraZeneca, Daiichi Sankyo, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01240070
Brief Title
Multifactorial Intervention in Type 2 Diabetes - Italy
Acronym
MINDIT
Official Title
Multicenter, Randomized Trial Designed to Evaluate the Applicability of the Guidelines of the Italian Society of Diabetology for the Prevention of Cardiovascular Diseases in Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
October 2010
Overall Recruitment Status
Unknown status
Study Start Date
January 2002 (undefined)
Primary Completion Date
December 2011 (Anticipated)
Study Completion Date
December 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University of Parma
Collaborators
Italian Society of Diabetology, AstraZeneca, Daiichi Sankyo, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Despite several clinical trials have clearly demonstrated that the correction of a single cardiovascular risk factor in patients with type 2 diabetes decreases the incidence of myocardial infarction and other cardiovascular disease (CVD) events, only the Steno study has been evaluating the effect of a multifactorial intervention strategy on macrovascular complications of diabetes. For this reason, the disease management approach currently endorsed by international guidelines (i.e correction of all major CVD risk factors to target levels usually lower than lower risk populations) has not been extensively investigated in terms of prevalence of application in current clinical practice and in terms of real efficacy. The Multifactorial INtervention in type 2 Diabetes - ITaly (MIND.IT) is a multicentric two-phase study involving 9 Diabetes Care Units throughout Italy with the overall aims of: (1) investigating the degree of application of the international guidelines for CVD prevention in type 2 diabetic patients and (2) verifying whether the application of an intensive multi-factorial intervention inspired by these guidelines is feasible and effective in decreasing the incidence of new CVD events.
Detailed Description
The study is multi-centric, randomized, open label, active treatment controlled, two parallel-group, pragmatical intervention trial with 5 years of follow-up, to assess superiority of an intensive treat-to-target strategy (including lifestyle and pharmacological interventions) for correction of major cardiovascular risk factors compared to usual care in decreasing incidence of first cardiovascular events in non complicated type 2 diabetic patients at high risk, as defined by presence of 2 or more cardiovascular risk factors. All high-risk patients identified during phase 1 who accepted to participated were allocated to usual or intensive treatment based on the recruiting center. Centers were randomly assigned to treatment arm before phase 2 beginning. Investigators from Intensive Care centers received centralized training to ensure the application of the intensive care program on their patients. HbA1c values and lipid profile are assessed in peripheral laboratories (one per each study site) with an external, centralized, quality control program and the adjustment for systematic differences among study labs. Participating investigators are left free to decide upon patient's treatments. In intensive-care centers, investigators are provided with a multi-factorial step-wise protocol to support the application of a treat-to-target approach. Intensive care strategy includes intervention on lifestyle. Dietary intervention goals: BMI<25 or 5% reduction of body weight; dietary assumption of saturated fat <10% of total caloric intake; fibers= 15-20 g/1000 Kcal. Methods defined to reach the dietary goal: A) Patients with BMI 25-30 kg/m2: reduction of caloric intake = 300-500 Cal/d; B) Patients with BMI >30: reduction of caloric intake 500-800 Cal/d. Physical activity intervention goal: 200-300 calories per day. Example: brisk walking for 30 min every day or biking (18-25Km/h 45-60 min). Alternatives: swimming 1h , dancing 1h, gym exercise 1h;-avoiding isometric exercise and exercise with intensity >50-60 % of maximal oxygen consumption. Frequency: everyday or at least 3 times a week; Pharmacological intervention: Blood glucose control, multi-step intervention. In obese patients: 1) Metformin (M, 500-2500mg); 2) M+Sulphonylureas (S) or S-like drugs, increasing progressively the dose; 3) M+S+Acarbose; 4) M+S+insulin bed-time; 5) insulin basal-bolus. In normal weight patients: 1) S; 2) S+acarbose; 3) S+ bed-time insulin; 4) insulin basal bolus; Blood pressure control --> 1) Ace-inhibitors or AT-II receptor antagonists; 2) add long acting calcium-channel blockers or beta-blockers or low dose diuretics; 3) add a third drug; lipid control: 1) diet + physical activity; 2) if LDL > 130 mg/dL statins (with a stepwise increase of dose if necessary); if triglycerides > 200 mg/dL fibrates; anti-platelet treatment: aspirin 100 mg/d in all patients (alternative drugs for aspirin-intolerants). The scheduled visits were defined as follows: Intensive-care group: mandatory visit every three months with annual visit for MIND.IT data collection. Usual-care group: at least one MIND.IT visit every year + the usual organization of the center.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
diabetes,, cardiovascular, risk factor, cardiovascular event, intervention

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1461 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Clinical practice in type 2 diabetes treatment
Arm Title
Intensive Care
Arm Type
Active Comparator
Arm Description
Intensive multi-factorial treat-to-target intervention, according to international guidelines, that includes both lifestyle intervention and a step-wise strategy for pharmacological treatment with a treat-to-target approach.
Intervention Type
Other
Intervention Name(s)
Intensive care
Intervention Description
Intensive multi-factorial treat-to-target intervention program designed according to international guidelines
Primary Outcome Measure Information:
Title
Cardiovascular events
Description
To verify if an intensive care intervention compared to usual care is able to significantly decrease the incidence of first cardiovascular event. Composite primary end-point = mortality for cardiovascular causes, proven acute myocardial infarction (STEMI or NSTEMI), acute coronary syndrome requiring hospitalization, proven ischemic stroke, coronary or carotid revascularization procedure
Time Frame
5 years of follow up
Secondary Outcome Measure Information:
Title
cardiovascular risk factors changes
Description
To assess whether the intensive treatment is able to significantly improve cardiovascular risk factors with increased multiple-target achievement. A pre-planned interim analysis after two years of follow-up was foreseen by the study protocol. To verify that the intesive protocol implemented on the basis of national and international guidelines is actually feasible in a real world clinical setting.
Time Frame
2 years and 5 years of follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Both genders age 50-70 years Type two diabetes with at least two-year history of disease and without insulin treatment in the first two years after diagnosis Negative medical history for documented previous cardiovascular events or macrovascular complications Written consent to participate Presence of at least 2 of the following risk factors: LDL cholesterol > 130 mg/dL (regardless of treatment) Triglycerides > 200 mg/dL HDL cholesterol < 35 (males) or 45 (females) mg/dL Blood pressure > 140/90 mmHg Cigarette smoking Exclusion Criteria: Age below 50 or above 70 years Type 1 diabetes, diagnosis before 40 years of age, known presence of auto-antibodies or insulin requirement in the first 2 years of disease. Chronic kidney failure (plasma creatinine > 2 mg/dL) Significant liver damage (AST and/or ALT > 2 times the upper limits of normality) History of previous cardiovascular events Active neoplasms or any concomitant disease limiting life expectancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ivana Zavaroni, MD
Organizational Affiliation
University of Parma
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Angela A Rivellese, MD
Organizational Affiliation
Federico II University of Naples
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Olga Vaccaro, MD
Organizational Affiliation
Federico II University of Naples
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Roberto Miccoli, MD
Organizational Affiliation
University of Pisa
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mariella Trovati, MD
Organizational Affiliation
University of Turin, Italy
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Franco Cavalot, MD
Organizational Affiliation
University of Turin, Italy
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Massimo Boemi, MD
Organizational Affiliation
INRCA of Ancona
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
PierPaolo DeFeo, MD
Organizational Affiliation
University Of Perugia
Official's Role
Study Director
Facility Information:
Facility Name
Francesco Giorgino
City
Bari
Country
Italy
Facility Name
Maria Dolci
City
Carrara
Country
Italy
Facility Name
Lamberto De Giorgio
City
La Spezia
Country
Italy
Facility Name
Giuseppe Derosa
City
Pavia
Country
Italy
Facility Name
PierPaolo DeFeo
City
Perugia
Country
Italy
Facility Name
Donatella Zavaroni
City
Piacenza
Country
Italy
Facility Name
Roberto Miccoli
City
Pisa
Country
Italy
Facility Name
Giovanni Ghirlanda
City
Roma
Country
Italy
Facility Name
Mariela Trovati
City
Torino
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
17426738
Citation
Rivellese AA, Boemi M, Cavalot F, Costagliola L, De Feo P, Miccoli R, Patti L, Trovati M, Vaccaro O, Zavaroni I; Mind.it Study Group. Dietary habits in type II diabetes mellitus: how is adherence to dietary recommendations? Eur J Clin Nutr. 2008 May;62(5):660-4. doi: 10.1038/sj.ejcn.1602755. Epub 2007 Apr 11.
Results Reference
background
PubMed Identifier
18093594
Citation
Vaccaro O, Boemi M, Cavalot F, De Feo P, Miccoli R, Patti L, Rivellese AA, Trovati M, Ardigo D, Zavaroni I; MIND-IT Study Group. The clinical reality of guidelines for primary prevention of cardiovascular disease in type 2 diabetes in Italy. Atherosclerosis. 2008 Jun;198(2):396-402. doi: 10.1016/j.atherosclerosis.2007.10.026. Epub 2008 Feb 21.
Results Reference
background
PubMed Identifier
23863908
Citation
Vaccaro O, Franzini L, Miccoli R, Cavalot F, Ardigo D, Boemi M, De Feo P, Reboldi G, Rivellese AA, Trovati M, Zavaroni I; MIND.IT Study Group. Feasibility and effectiveness in clinical practice of a multifactorial intervention for the reduction of cardiovascular risk in patients with type 2 diabetes: the 2-year interim analysis of the MIND.IT study: a cluster randomized trial. Diabetes Care. 2013 Sep;36(9):2566-72. doi: 10.2337/dc12-1781. Epub 2013 Jul 17.
Results Reference
derived
PubMed Identifier
23147277
Citation
Ardigo D, Vaccaro O, Cavalot F, Rivellese AA, Franzini L, Miccoli R, Patti L, Boemi M, Trovati M, Zavaroni I; MIND.IT study group. Effectiveness of treat-to-target strategy for LDL-cholesterol control in type 2 diabetes: post-hoc analysis of data from the MIND.IT study. Eur J Prev Cardiol. 2014 Apr;21(4):456-63. doi: 10.1177/2047487312467746. Epub 2012 Nov 12.
Results Reference
derived
Links:
URL
http://www.siditalia.it/forisid.html?start=2
Description
Official site of the ForiSid, where the study is briefly described in italian language

Learn more about this trial

Multifactorial Intervention in Type 2 Diabetes - Italy

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