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Exercise Program Combined or Not With Nutritional intErvention in Adults With tyPe 2 Diabetes (PEP-2)

Primary Purpose

Overweight, Obesity, Type 2 Diabetes

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Caloric restriction
Diet intervention and structured exercise training program
Sponsored by
Institut de Recherches Cliniques de Montreal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Overweight focused on measuring overweight, obesity, type 2 diabetes, caloric restriction, exercise program, epicardial fat

Eligibility Criteria

30 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Body mass index (BMI) 27-40 kg/m2
  • Type 2 diabetes diagnosed since at least 3 months
  • High risk of cardiovascular disease : Framingham global cardiovascular risk score for 10 years > 15% or 2 or more of the following risk factors: age > 50years, dyslipidemia or treatment, high blood pressure or treatment, pathologic microalbuminuria or established proteinuria, currently smoking, family history of early cardiovascular disease (< 60 years), inactivity or high waist circumference according to IDF criteria
  • HbA1c : 6.0-10.0%
  • Stable weight for last 3 months (±3kg) reported or documented
  • Stable treatment for diabetes. 4 weeks: blood pressure and dyslipidemia medications. 3 months: glitazones and weight loss drugs the treatment that will be maintained at the same dose during the study; insulin will have been introduced since 4 months at least and previous month dose should be stable defined as a 10% variation or less of total daily units.

Exclusion Criteria:

  • Pregnancy, breastfeeding
  • Type 1 diabetes
  • Secondary diabetes (e.g cystic fibrosis, steroid induced, etc.)
  • Recurrent, hypoglycemia without precursor signs or severe hypoglycemia occurred ≥ 2 times for last 12 months
  • Renal failure , creatinine clearance < 40 ml/min (MDRD)
  • Severe retinopathy or neuropathy that can contra-indicate exercise or expose patient to high risk of complications (e.g wound)
  • NYHA classification class III or IV of cardiac insufficiency
  • Established coronaropathy
  • Non stable ventricular or supra-ventricular arrythmia
  • Severe limb atherosclerosis or previous amputation
  • Recent (< 12 months) diagnosis of cancer excepted thyroid and skin
  • Major mental disease
  • Drugs with established effects on weigh such as megace®

Sites / Locations

  • Institut de recherches cliniques de Montréal (IRCM)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Active Comparator

Active Comparator

Arm Label

Optimized usual care

Diet intervention alone

diet intervention and exercise program

Arm Description

participants will attend one visit with the dietician (30mn) and the physical activity specialist (30mn) when they will be given Canadian guidelines pamphlets for physical activity and food consumption. They will also receive a phone call once a month to discuss about issues in guidelines following.

Participants will attend one visit with the physical activity specialist (30mn) when they will receive the physical activity guidelines. Monthly phone call will be make to discuss about issues in physical activity guidelines following.These individuals will also be enrolled in a supervised caloric restriction program. They will have to visit the dietician once a week for the first months and then twice a month for 3 months. The diet intervention will focus on a low fat diet. At each session participants will be weighed and taken the blood pressure.

Participants will attend diet intervention as described for group 2. They will also follow a supervised exercise program three days per week for 4 months. The exercise training is an interval high intensity aerobic (85-90% heart rate reserve) program with resistance exercises (15RM, 2-3 repetitions). Each session will last one hour. At the end of month 1, 2, and 3, all participants will receive the SWA armband for 7 days to record physical activity and estimate energy expenditure. At the end of Month 4, all participants will attend a study visit for repeat baseline testing.

Outcomes

Primary Outcome Measures

Total fat mass
Total fat mass (kg) assessed by Dual X-Ray absoptiometry (DXA)

Secondary Outcome Measures

Diabetes control
A1c and fasting plasma glucose
Epicardial fat
Epicardial fat thickness measured by simplified cardiac echography
Body composition
Body composition : trunkal fat mass, apendicular fat mass, lean body mass and estimated visceral fat mass determined by DXA
Energy consumption
Energy consumption : as measured by total calories consumed using a three non consecutive days food journal. The three days should include one week-end day.
Resting metabolic rate
Resting metabolic rate determined by indirect calorimetry.
Total energy expenditure
Total energy expenditure estimated from 7 days accelerometer data (Senwear Armband accelerometer).
Physical activity energy expenditure
Physical activity energy expenditure estimated from 7 days accelerometer data (Senwear Armband accelerometer).
Muscle strength
upper and lower body strength using 1-RM technique
Cardiorespiratory fitness
Participants will perform a graded exercise test on a cycle ergometer to voluntary exhaustion. Peak oxygen consumption (VO2peak) will be considered to be the highest value obtained during the test.
Lipid profile
Total cholesterol, LDL-Cholesterol, HDL-cholesterol (HDL-C), Triglycerides, Apolipoprotein B, ratios TG/HDL-C and Total cholesterol/HDL-C will be determined with fasting veinous blood sample
Biochemical hepatic steatosis score
Blood pressure
systolic and diastolic blood pressure
Hormonal profile
Inflammatory profile
Psychosocial profile
questionnaire addressing : body esteem, self-esteem, stress, dietary restraint, disinhibition, hunger, quality of life, self-efficacy,perceived benefits, perceived risks
Diabetes self-care
Summary of diabetes care activities (SDCA) questionnaire
visceral fat thickness

Full Information

First Posted
August 20, 2010
Last Updated
April 18, 2016
Sponsor
Institut de Recherches Cliniques de Montreal
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1. Study Identification

Unique Protocol Identification Number
NCT01186952
Brief Title
Exercise Program Combined or Not With Nutritional intErvention in Adults With tyPe 2 Diabetes
Acronym
PEP-2
Official Title
Effects of an Exercise Program Combined or Not With Nutritional intErvention on Total Fat, Epicardial Fat and Metabolic Profile of Obese and Overweight Adults With tyPe 2 Diabetes (The PEP-2 Study)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
September 2010 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institut de Recherches Cliniques de Montreal

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Inactivity and excess energy consumption are leading causes of obesity and type 2 diabetes which are associated with increased cardio-metabolic risk. In order to reduce the cardiovascular risk associated with type 2 diabetes, the Canadian Diabetes Association guidelines (2008) recommends weight loss through caloric restriction and structured physical activity. However, the comparative effects of different methods to obtain caloric deficit for weight loss remains to be elucidated. The main objective of this study is to assess the impact of two strategies of caloric deficit: diet alone or diet and exercise on total fat mass, epicardial fat and cardiovascular risk factors in overweight and obese adults with type 2 diabetes and at high risk of cardiovascular disease.
Detailed Description
Type 2 diabetes is mainly caused by excess body weight due to lack of physical activity and high amount of calories consumption. Individuals with type 2 diabetes demonstrated increased risk of cardiovascular disease compared to non diabetic. Studies showed a cardiovascular risk reduction after weight loss among individuals at risk through lifestyle modification: increase physical activity and low calorie diet. Favourable effects of weight loss on cardiovascular risk are mainly due to total body fat reduction. However, the location of body fat excess has also some important implications. It is now well known that abdominal (visceral) and ectopic fat accumulation (e.g. hepatic fat, epicardial fat, etc.) are more related to an unfavorable cardio-metabolic profile than total fat mass. It has been demonstrated that a moderate weight loss obtained with physical activity or caloric restriction is related to a significant reduction of ectopic fat mass. However, ectopic fat measurement remains problematic due to lack of standardization and safety issues (X-ray). Epicardial fat thickness measured by simple echocardiography is a reliable method to evaluate ectopic fat accumulation. Little research have been done to assess the effect of different methods of weight loss on total fat as well as ectopic fat specifically epicardial adipose tissue among individuals with type 2 diabetes. The objective of this study is to compare to a control group with detailed advice the impact of two structured strategies of caloric deficit: diet alone or diet and exercise on total fat mass, epicardial fat and cardiovascular risk factors in overweight and obese adults with type 2 diabetes and at high risk of cardiovascular disease. The participants to the present study will be free-living adults overweight and obese with type 2 diabetes and at high risk of cardiovascular disease as determined by a Framingham risk score above 15% or the presence of two or more cardiovascular risk factors. Participants will attend a screening study visit to confirm eligibility criteria (anthropometric variables, blood pressure, complete physical examination, coronary heart disease diagnostic by echocardiogram, physical activity aptitude). After enrollment, a baseline visit will consist in series of data collection such as : anthropometric variables, blood pressure, cycle ergometer test to evaluate cardiovascular fitness, an echocardiography to determine epicardial fat thickness, a dual energy x-ray absorptiometry (DEXA) scan to assess body fat, lean mass and bone density, indirect calorimetry for resting metabolic rate, physical activity profile and total energy expenditure determined by Sense Wear Armband (SWA) accelerometer (7days), food consumption estimate with 3 days dairy, questionnaires addressing sociodemographic and psychosocial characteristics, diabetes self-care (SDCA questionnaire), a blood and urine collection for diabetes control, hepatic steatosis biochemical score, detailed lipids, hormonal and inflammatory profile and finally microalbuminuria. The body composition will also be measured by impedancemetry and BOD-POD. Participants will then be randomly assigned to one of the three groups of the study : Group 1: Counseling for physical activity and healthy eating Group 2: Structured diet intervention (caloric restriction) and counseling for physical activity Group 3: Structured diet intervention (caloric restriction) and structured exercise training program (aerobic and resistance training). Group 1: participants will attend one visit with the dietician (30mn) and the physical activity specialist (30mn) when they will be given Canadian guidelines pamphlets for physical activity and food consumption. They will also receive a phone call once a month to discuss about issues in guidelines following. Group 2: participants will attend one visit with the physical activity specialist (30mn) when they will receive the physical activity guidelines. Monthly phone call will be make to discuss about issues in physical activity guidelines following. These individuals will also be enrolled in a supervised caloric restriction program. They will have to visit the dietician once a week for the first months and then twice a month for 3 months. The diet intervention will focus on a low fat diet. At each session participants will be weighed and taken the blood pressure. Group 3: participants will attend diet intervention as described for group 2. They will also follow a supervised exercise program three days per week for 4 months. The exercise training is an interval high intensity aerobic (85-90% Heart rate reserve) program with resistance exercises (15RM, 2-3 repetitions). Each session will last one hour. At the end of month 1, 2, and 3, all participants will receive the SWA armband for 7 days to record physical activity and estimate energy expenditure. At the end of Month 4, all participants will attend a study visit for repeat baseline testing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight, Obesity, Type 2 Diabetes
Keywords
overweight, obesity, type 2 diabetes, caloric restriction, exercise program, epicardial fat

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Optimized usual care
Arm Type
No Intervention
Arm Description
participants will attend one visit with the dietician (30mn) and the physical activity specialist (30mn) when they will be given Canadian guidelines pamphlets for physical activity and food consumption. They will also receive a phone call once a month to discuss about issues in guidelines following.
Arm Title
Diet intervention alone
Arm Type
Active Comparator
Arm Description
Participants will attend one visit with the physical activity specialist (30mn) when they will receive the physical activity guidelines. Monthly phone call will be make to discuss about issues in physical activity guidelines following.These individuals will also be enrolled in a supervised caloric restriction program. They will have to visit the dietician once a week for the first months and then twice a month for 3 months. The diet intervention will focus on a low fat diet. At each session participants will be weighed and taken the blood pressure.
Arm Title
diet intervention and exercise program
Arm Type
Active Comparator
Arm Description
Participants will attend diet intervention as described for group 2. They will also follow a supervised exercise program three days per week for 4 months. The exercise training is an interval high intensity aerobic (85-90% heart rate reserve) program with resistance exercises (15RM, 2-3 repetitions). Each session will last one hour. At the end of month 1, 2, and 3, all participants will receive the SWA armband for 7 days to record physical activity and estimate energy expenditure. At the end of Month 4, all participants will attend a study visit for repeat baseline testing.
Intervention Type
Behavioral
Intervention Name(s)
Caloric restriction
Other Intervention Name(s)
Structured diet intervention (caloric restriction)
Intervention Description
The caloric restriction diet will follow the Canadian Diabetes Association guidelines and be nutritionally balanced with a reduced total fat as well as saturated content.
Intervention Type
Behavioral
Intervention Name(s)
Diet intervention and structured exercise training program
Other Intervention Name(s)
diet intervention and exercise program.
Intervention Description
Participants will follow the diet intervention previously described and a supervised physical activity program. The supervised exercise training sessions will take place three times a week for 4 months. Each session will last 1hour and will include aerobic exercise and resistance training. The aerobic training program will be treadmills intervals exercise at 50-70 % of heart rate reserve(HRR) the first month and 85-90% of HRR from the second to the fourth month. The resistance training programme will consist of two to three sets of 12 repetitions of the following exercises: leg press, chest press, lat pulldown, shoulder press, biceps curl, triceps extension.
Primary Outcome Measure Information:
Title
Total fat mass
Description
Total fat mass (kg) assessed by Dual X-Ray absoptiometry (DXA)
Time Frame
month 4
Secondary Outcome Measure Information:
Title
Diabetes control
Description
A1c and fasting plasma glucose
Time Frame
month 4
Title
Epicardial fat
Description
Epicardial fat thickness measured by simplified cardiac echography
Time Frame
month 4
Title
Body composition
Description
Body composition : trunkal fat mass, apendicular fat mass, lean body mass and estimated visceral fat mass determined by DXA
Time Frame
month 4
Title
Energy consumption
Description
Energy consumption : as measured by total calories consumed using a three non consecutive days food journal. The three days should include one week-end day.
Time Frame
month 4
Title
Resting metabolic rate
Description
Resting metabolic rate determined by indirect calorimetry.
Time Frame
month 4
Title
Total energy expenditure
Description
Total energy expenditure estimated from 7 days accelerometer data (Senwear Armband accelerometer).
Time Frame
month 2,3,4
Title
Physical activity energy expenditure
Description
Physical activity energy expenditure estimated from 7 days accelerometer data (Senwear Armband accelerometer).
Time Frame
month 2,3,4
Title
Muscle strength
Description
upper and lower body strength using 1-RM technique
Time Frame
month 4
Title
Cardiorespiratory fitness
Description
Participants will perform a graded exercise test on a cycle ergometer to voluntary exhaustion. Peak oxygen consumption (VO2peak) will be considered to be the highest value obtained during the test.
Time Frame
month 4
Title
Lipid profile
Description
Total cholesterol, LDL-Cholesterol, HDL-cholesterol (HDL-C), Triglycerides, Apolipoprotein B, ratios TG/HDL-C and Total cholesterol/HDL-C will be determined with fasting veinous blood sample
Time Frame
month 4
Title
Biochemical hepatic steatosis score
Time Frame
month 4
Title
Blood pressure
Description
systolic and diastolic blood pressure
Time Frame
month 4
Title
Hormonal profile
Time Frame
month 4
Title
Inflammatory profile
Time Frame
month 4
Title
Psychosocial profile
Description
questionnaire addressing : body esteem, self-esteem, stress, dietary restraint, disinhibition, hunger, quality of life, self-efficacy,perceived benefits, perceived risks
Time Frame
month 4
Title
Diabetes self-care
Description
Summary of diabetes care activities (SDCA) questionnaire
Time Frame
month 4
Title
visceral fat thickness
Time Frame
month 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Body mass index (BMI) 27-40 kg/m2 Type 2 diabetes diagnosed since at least 3 months High risk of cardiovascular disease : Framingham global cardiovascular risk score for 10 years > 15% or 2 or more of the following risk factors: age > 50years, dyslipidemia or treatment, high blood pressure or treatment, pathologic microalbuminuria or established proteinuria, currently smoking, family history of early cardiovascular disease (< 60 years), inactivity or high waist circumference according to IDF criteria HbA1c : 6.0-10.0% Stable weight for last 3 months (±3kg) reported or documented Stable treatment for diabetes. 4 weeks: blood pressure and dyslipidemia medications. 3 months: glitazones and weight loss drugs the treatment that will be maintained at the same dose during the study; insulin will have been introduced since 4 months at least and previous month dose should be stable defined as a 10% variation or less of total daily units. Exclusion Criteria: Pregnancy, breastfeeding Type 1 diabetes Secondary diabetes (e.g cystic fibrosis, steroid induced, etc.) Recurrent, hypoglycemia without precursor signs or severe hypoglycemia occurred ≥ 2 times for last 12 months Renal failure , creatinine clearance < 40 ml/min (MDRD) Severe retinopathy or neuropathy that can contra-indicate exercise or expose patient to high risk of complications (e.g wound) NYHA classification class III or IV of cardiac insufficiency Established coronaropathy Non stable ventricular or supra-ventricular arrythmia Severe limb atherosclerosis or previous amputation Recent (< 12 months) diagnosis of cancer excepted thyroid and skin Major mental disease Drugs with established effects on weigh such as megace®
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Remi Rabasa-Lhoret, MD, PhD
Organizational Affiliation
Institut de Recherches Cliniques de Montreal
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Antony Karelis, PhD
Organizational Affiliation
Université de Québec à Montréal
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Denis Prud'Homme, MD, Msc
Organizational Affiliation
University of Ottawa
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Eric Doucet, PhD
Organizational Affiliation
University of Ottawa
Official's Role
Study Chair
Facility Information:
Facility Name
Institut de recherches cliniques de Montréal (IRCM)
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H2W 1R7
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
33549453
Citation
Leroux-Stewart J, Elisha B, Tagougui S, Suppere C, Bernard S, Mircescu H, Desjardin K, Messier V, Iacobellis G, Rabasa-Lhoret R. Effect of caloric restriction with or without physical activity on body composition and epicardial fat in type 2 diabetic patients: A pilot randomized controlled trial. Nutr Metab Cardiovasc Dis. 2021 Mar 10;31(3):921-929. doi: 10.1016/j.numecd.2020.11.005. Epub 2020 Nov 13.
Results Reference
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Exercise Program Combined or Not With Nutritional intErvention in Adults With tyPe 2 Diabetes

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