search
Back to results

Feasibility of Prediabetes Remission in Adults With Coronary Heart Disease (DIABEPIC1)

Primary Purpose

Prediabetic State, Coronary Heart Disease, Healthy Lifestyle

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Lifestyle changes
Sponsored by
Montreal Heart Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prediabetic State

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Coronary heart disease patients referred from the Montreal Heart Institute.
  • Aged ≥ 40 years.
  • Recently diagnosed prediabetes (HbA1c ≥ 5.7% to 6.4%) in the last 6 months.
  • Referred to Centre EPIC because of stable angina, acute coronary syndrome (with or without ST elevation), after coronary revascularization (primary or elective) or bypass surgery.
  • Able to perform a maximal exercise test and exercise training program in accordance with current cardiovascular rehabilitation recommendations.
  • Able to use a smartphone application or to complete an adherence/compliance diary.
  • Able to read, understand and sign the information and consent form.

Exclusion Criteria:

  • Absolute and relative contraindication to exercise testing and/or physical training.
  • Diabetic patients (HbA1c ≥ 6.5%) or patients with a HbA1c value of ≥ 5.7% to 6.4% but with the help of oral hypoglycemic agents.
  • Taking psychotropic medications that may induce mass gain (tricyclic antidepressants, mirtazapine, paroxetine, lithium, valproate, clozapine, olanzapine) or other medications known to promote mass gain (cortisone).
  • Taking recently introduced weight-loss medications (semaglutide).
  • Unintentional mass loss of more than 10 kg in the past year.
  • Pregnant or nursing women.

Sites / Locations

  • Preventive medicine and physical activity centre (centre EPIC), Montreal Heart InstituteRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention

Arm Description

Behavioral: Lifestyle changes Nutritional advice to progressively integrate a moderate-carbohydrate Mediterranean diet with intermittent fasting 16:8 (5 times/week for 12 weeks). Personalized exercise prescription and training (3 times per week) Personalized education and motivational interviewing

Outcomes

Primary Outcome Measures

Feasibility of an intensive multidisciplinary program based on lifestyle changes in coronary heart disease patients recently diagnosed with prediabetes that are referred to the Centre EPIC.
Total recruitment, recruitment rate, compliance and completion rate at 3 months after the start of the intervention
Feasibility of an intensive multidisciplinary program based on lifestyle changes in coronary heart disease patients recently diagnosed with prediabetes that are referred to the Centre EPIC.
Total recruitment, recruitment rate, compliance and completion rate at 6 months after the start of the intervention

Secondary Outcome Measures

Proportion of prediabetic participants (HbA1c ≥ 5.7% to 6.4% at the start of the program) in complete remission of prediabetes.
Remission of prediabetes will be defined by the following 3 criteria: An HbA1c < 5.7% at 3 months of intervention (Metabolic criteria). Which is maintained at 6 months (Duration criteria). Without the use of glucose-lowering agents (pharmacological criteria). Proportion of prediabetic patients that reach an HbA1c < 5.7% at 6 months of intervention will also be studied
Evolution of the HOMA-IR between the start of the program, the end of intervention (3 months) and the follow-up visit (6 months).
HOMA-IR is a marker of insulin resistance

Full Information

First Posted
June 22, 2022
Last Updated
July 12, 2022
Sponsor
Montreal Heart Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT05459987
Brief Title
Feasibility of Prediabetes Remission in Adults With Coronary Heart Disease
Acronym
DIABEPIC1
Official Title
Feasibility and Impact of an Intensive Team-based Intervention on Prediabetes Remission in Patients With Coronary Heart Disease
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 15, 2022 (Actual)
Primary Completion Date
March 15, 2023 (Anticipated)
Study Completion Date
June 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Montreal Heart Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To evaluate the feasibility of a 6-month multidisciplinary program to reverse prediabetes in adults with coronary heart disease using the Mediterranean diet, intermittent fasting and exercise.
Detailed Description
The proposed study will assess the feasibility of an intensive lifestyle program to reverse newly onset prediabetes (HbA1c ≥ 5.7% to 6.4%) in patients with coronary heart disease that would otherwise start a standard cardiac rehabilitation programme (12 weeks with twice weekly exercise, nutrition, and nursing counselling). The patients will be offered an upgraded 6-month intensive team-based multidisciplinary stepwise program with the goal of remitting prediabetes. The program will consist of a 3-month synchronous nutritional, exercise, and motivational intervention and of a 3-month maintenance and follow-up period. The DIABEPIC prevent 1 study is a single-arm, open-label study aiming to demonstrate the feasibility of an intensive multidisciplinary stepwise intervention in newly diagnosed prediabetic and coronary heart disease patients, ultimately aiming to remit prediabetes. The purpose of this first study is to devise and iteratively improve participant recruitment and adherence strategies for a possible future randomized controlled trial. It also includes as goals: to study the efficacy and adherence of an intensive multicomponent lifestyle intervention, to study the proportion of patients that improve or remit their insulin resistant state, to study the changes in a variety of anthropomorphic, physical, analytic, vascular and test parameters and to better characterize the factors associated with prediabetes remission.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetic State, Coronary Heart Disease, Healthy Lifestyle, Remission

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Behavioral: Lifestyle changes Nutritional advice to progressively integrate a moderate-carbohydrate Mediterranean diet with intermittent fasting 16:8 (5 times/week for 12 weeks). Personalized exercise prescription and training (3 times per week) Personalized education and motivational interviewing
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle changes
Intervention Description
Nutritional advice to progressively integrate a moderate-carbohydrate Mediterranean diet with intermittent fasting 16:8 (5 times/week for 12 weeks). Personalized exercise prescription and training (3 times per week) Personalized education and motivational interviewing
Primary Outcome Measure Information:
Title
Feasibility of an intensive multidisciplinary program based on lifestyle changes in coronary heart disease patients recently diagnosed with prediabetes that are referred to the Centre EPIC.
Description
Total recruitment, recruitment rate, compliance and completion rate at 3 months after the start of the intervention
Time Frame
at 3 months after the start of the intervention
Title
Feasibility of an intensive multidisciplinary program based on lifestyle changes in coronary heart disease patients recently diagnosed with prediabetes that are referred to the Centre EPIC.
Description
Total recruitment, recruitment rate, compliance and completion rate at 6 months after the start of the intervention
Time Frame
at 6 months after the start of the intervention
Secondary Outcome Measure Information:
Title
Proportion of prediabetic participants (HbA1c ≥ 5.7% to 6.4% at the start of the program) in complete remission of prediabetes.
Description
Remission of prediabetes will be defined by the following 3 criteria: An HbA1c < 5.7% at 3 months of intervention (Metabolic criteria). Which is maintained at 6 months (Duration criteria). Without the use of glucose-lowering agents (pharmacological criteria). Proportion of prediabetic patients that reach an HbA1c < 5.7% at 6 months of intervention will also be studied
Time Frame
at 3 and 6 months of the start of the intervention
Title
Evolution of the HOMA-IR between the start of the program, the end of intervention (3 months) and the follow-up visit (6 months).
Description
HOMA-IR is a marker of insulin resistance
Time Frame
at 3 and 6 months of the start of the intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Coronary heart disease patients referred from the Montreal Heart Institute. Aged ≥ 40 years. Recently diagnosed prediabetes (HbA1c ≥ 5.7% to 6.4%) in the last 6 months. Referred to Centre EPIC because of stable angina, acute coronary syndrome (with or without ST elevation), after coronary revascularization (primary or elective) or bypass surgery. Able to perform a maximal exercise test and exercise training program in accordance with current cardiovascular rehabilitation recommendations. Able to use a smartphone application or to complete an adherence/compliance diary. Able to read, understand and sign the information and consent form. Exclusion Criteria: Absolute and relative contraindication to exercise testing and/or physical training. Diabetic patients (HbA1c ≥ 6.5%) or patients with a HbA1c value of ≥ 5.7% to 6.4% but with the help of oral hypoglycemic agents. Taking psychotropic medications that may induce mass gain (tricyclic antidepressants, mirtazapine, paroxetine, lithium, valproate, clozapine, olanzapine) or other medications known to promote mass gain (cortisone). Taking recently introduced weight-loss medications (semaglutide). Unintentional mass loss of more than 10 kg in the past year. Pregnant or nursing women.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Louis Bherer, PhD
Phone
5148273758
Email
louis.bherer@umontreal.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louis Bherer, PhD
Organizational Affiliation
Université de Montréal
Official's Role
Principal Investigator
Facility Information:
Facility Name
Preventive medicine and physical activity centre (centre EPIC), Montreal Heart Institute
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H1T1N6
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Louis Bherer, PhD
Phone
514-827-3758
Email
louis.bherer@umontreal.ca
First Name & Middle Initial & Last Name & Degree
Louis Bherer, PhD
First Name & Middle Initial & Last Name & Degree
Martin Juneau, MD
First Name & Middle Initial & Last Name & Degree
Josep Iglesies-Grau, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
If sponsor OK, we would agree with making individual data available to other researchers
IPD Sharing Time Frame
One year after completion of the study
IPD Sharing Access Criteria
Upon request to the principal investigator
Citations:
PubMed Identifier
31518657
Citation
Saeedi P, Petersohn I, Salpea P, Malanda B, Karuranga S, Unwin N, Colagiuri S, Guariguata L, Motala AA, Ogurtsova K, Shaw JE, Bright D, Williams R; IDF Diabetes Atlas Committee. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas, 9th edition. Diabetes Res Clin Pract. 2019 Nov;157:107843. doi: 10.1016/j.diabres.2019.107843. Epub 2019 Sep 10.
Results Reference
background
PubMed Identifier
29475843
Citation
Bommer C, Sagalova V, Heesemann E, Manne-Goehler J, Atun R, Barnighausen T, Davies J, Vollmer S. Global Economic Burden of Diabetes in Adults: Projections From 2015 to 2030. Diabetes Care. 2018 May;41(5):963-970. doi: 10.2337/dc17-1962. Epub 2018 Feb 23.
Results Reference
background
PubMed Identifier
31105044
Citation
Hall KD, Ayuketah A, Brychta R, Cai H, Cassimatis T, Chen KY, Chung ST, Costa E, Courville A, Darcey V, Fletcher LA, Forde CG, Gharib AM, Guo J, Howard R, Joseph PV, McGehee S, Ouwerkerk R, Raisinger K, Rozga I, Stagliano M, Walter M, Walter PJ, Yang S, Zhou M. Ultra-Processed Diets Cause Excess Calorie Intake and Weight Gain: An Inpatient Randomized Controlled Trial of Ad Libitum Food Intake. Cell Metab. 2019 Jul 2;30(1):67-77.e3. doi: 10.1016/j.cmet.2019.05.008. Epub 2019 May 16. Erratum In: Cell Metab. 2019 Jul 2;30(1):226. Cell Metab. 2020 Oct 6;32(4):690.
Results Reference
background
PubMed Identifier
31722562
Citation
Dal Canto E, Ceriello A, Ryden L, Ferrini M, Hansen TB, Schnell O, Standl E, Beulens JW. Diabetes as a cardiovascular risk factor: An overview of global trends of macro and micro vascular complications. Eur J Prev Cardiol. 2019 Dec;26(2_suppl):25-32. doi: 10.1177/2047487319878371. Epub 2019 Nov 13.
Results Reference
background
PubMed Identifier
27841877
Citation
Lotta LA, Gulati P, Day FR, Payne F, Ongen H, van de Bunt M, Gaulton KJ, Eicher JD, Sharp SJ, Luan J, De Lucia Rolfe E, Stewart ID, Wheeler E, Willems SM, Adams C, Yaghootkar H; EPIC-InterAct Consortium; Cambridge FPLD1 Consortium; Forouhi NG, Khaw KT, Johnson AD, Semple RK, Frayling T, Perry JR, Dermitzakis E, McCarthy MI, Barroso I, Wareham NJ, Savage DB, Langenberg C, O'Rahilly S, Scott RA. Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance. Nat Genet. 2017 Jan;49(1):17-26. doi: 10.1038/ng.3714. Epub 2016 Nov 14.
Results Reference
background

Learn more about this trial

Feasibility of Prediabetes Remission in Adults With Coronary Heart Disease

We'll reach out to this number within 24 hrs