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The Pre-Diabetes Interventions and Continued Tracking to Ease-out Diabetes (Pre-DICTED) Program

Primary Purpose

Pre-diabetes

Status
Active
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
Lifestyle modification
Metformin
Financial incentives
Sponsored by
Singapore General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pre-diabetes

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Singapore citizens or permanent residents
  2. Age between 18 and 64
  3. Body mass index (BMI) ≥ 23.0 kg/m2
  4. Pre-diabetes diagnosed based on:

    1. fasting plasma glucose 6.1 - 6.9 mmol/L (Impaired fasting glucose; IFG) and/or
    2. 2-hr plasma glucose in 75g oral glucose tolerance test (OGTT) 7.8 - 11.0 mmol/L (Impaired glucose tolerance; IGT) (Laboratory tests to be done within 6 months of enrolment)

Exclusion Criteria:

  1. Individuals with diabetes mellitus
  2. Health conditions impeding participation in lifestyle change programme (e.g. active cancer, recent myocardial event within 6 months, heart failure, chronic kidney disease)
  3. Current pregnancy or breast feeding
  4. Treatment with medications known to alter glucose tolerance
  5. Known allergic reaction to metformin

Sites / Locations

  • Singapore General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Treatment arm

Control

Arm Description

Participants in the treatment arm will receive structured group-based lifestyle interventions with stepwise addition of metformin for selected high-risk participants.

Participants in the control arm will receive the current standard of care for pre-diabetes which includes counseling on lifestyle modifications and follow up by primary care physicians.

Outcomes

Primary Outcome Measures

Diabetes incidence
The primary outcome, diabetes incidence, will be diagnosed based on a single, annual OGTT or the semi-annual FPG (Fasting plasma glucose) test

Secondary Outcome Measures

Weight
Weight in kg
Waist circumference
Waist circumference in cm
HbA1c
HbA1c in %
Fasting plasma glucose
Fasting plasma glucose in mmol/L
2-hour plasma glucose
2-hour plasma glucose post oral glucose challenge in mmol/L
International physical activity questionnaire (IPAQ) score
IPAQ score in MET minutes a week
Metformin adherence
Metformin adherence assessed by pill counts

Full Information

First Posted
October 13, 2017
Last Updated
May 4, 2022
Sponsor
Singapore General Hospital
Collaborators
Ministry of Health, Singapore, Health Promotion Board, Singapore, Singapore Clinical Research Institute, Duke-NUS Graduate Medical School
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1. Study Identification

Unique Protocol Identification Number
NCT03503942
Brief Title
The Pre-Diabetes Interventions and Continued Tracking to Ease-out Diabetes (Pre-DICTED) Program
Official Title
The Pre-Diabetes Interventions and Continued Tracking to Ease-out Diabetes (Pre-DICTED) Program
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 30, 2017 (Actual)
Primary Completion Date
March 30, 2024 (Anticipated)
Study Completion Date
April 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Singapore General Hospital
Collaborators
Ministry of Health, Singapore, Health Promotion Board, Singapore, Singapore Clinical Research Institute, Duke-NUS Graduate Medical School

4. Oversight

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

5. Study Description

Brief Summary
The Pre-DICTED (Pre-Diabetes Intervention and Continued Tracking to Ease-out Diabetes) program is a community-based diabetes prevention program. This study aims to test the effectiveness of structured, group-based lifestyle interventions with stepwise addition of metformin, if required, among subjects with pre-diabetes in multi-ethnic Singapore.
Detailed Description
The Pre-DICTED program is designed as a randomized, controlled, pragmatic trial. The program targets to recruit up to 846 overweight/obese (BMI ≥23.0) adults (age 18-64) with isolated impaired fasting glucose (IFG), isolated impaired glucose tolerance (IGT), or IFG + IGT in Singapore. The follow-up period will be 3 years. Eligible subjects will be identified through community, primary care clinics and hospital-based diabetes screening program. Following informed consent, eligible participants will be randomised into the control or the treatment arm. Participants in the control arm will receive the current standard of care for pre-diabetes which includes counseling on lifestyle modifications and follow up by primary care physicians. Participants in the treatment arm will undergo a 3-month, locally tailored, group-based lifestyle intervention program (consisting of nutrition workshops, exercise sessions and goal-setting workshop) plus subsequent stepwise addition of metformin for selected participants at the highest risk of progression to diabetes at ≥ 6 months of follow-up. Financial incentives will be awarded to participants who achieve weight lost of ≥5% of baseline weight during follow-up period. The primary outcome of diabetes incidence will be assessed bi-annually and compared across the study arms. Secondary outcomes will include weight, waist circumference, fasting plasma glucose (FPG), 2-h glucose, HbA1c, physical activity, diet and metformin adherence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pre-diabetes

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Treatment arm
Arm Type
Experimental
Arm Description
Participants in the treatment arm will receive structured group-based lifestyle interventions with stepwise addition of metformin for selected high-risk participants.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants in the control arm will receive the current standard of care for pre-diabetes which includes counseling on lifestyle modifications and follow up by primary care physicians.
Intervention Type
Behavioral
Intervention Name(s)
Lifestyle modification
Intervention Description
Participants in the treatment arm will receive structured, locally tailored, group-based lifestyle interventions that consist of a core intervention phase (3 months) and a maintenance phase (33 months). The core intervention phase will consist of twice weekly group sessions on nutrition, exercise and goal-setting within the first 6 weeks followed by 6 weeks of self-directed lifestyle modification. During the maintenance phase, the participants will receive monthly short message service (SMS) on health tips as well as 6 monthly telephone calls from program coordinators.
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin will be will be prescribed to treatment group participants at highest risk of diabetes conversion (i.e.IFG + IGT or IFG + HbA1c ≥6.0%) after at least 6 months of lifestyle interventions at a starting dose of 250 mg twice a day followed by up-titration to 500 mg twice a day after 3 months if the participants do not experience any gastrointestinal side effects.
Intervention Type
Other
Intervention Name(s)
Financial incentives
Intervention Description
Participants will be given cash incentives if they meet the weight loss target, which is pre-defined as 5% of baseline weight, at the 3rd, 6th, 12th, 18th, 24th, 30th and 36th month of study period.
Primary Outcome Measure Information:
Title
Diabetes incidence
Description
The primary outcome, diabetes incidence, will be diagnosed based on a single, annual OGTT or the semi-annual FPG (Fasting plasma glucose) test
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Weight
Description
Weight in kg
Time Frame
3 years
Title
Waist circumference
Description
Waist circumference in cm
Time Frame
3 years
Title
HbA1c
Description
HbA1c in %
Time Frame
3 years
Title
Fasting plasma glucose
Description
Fasting plasma glucose in mmol/L
Time Frame
3 years
Title
2-hour plasma glucose
Description
2-hour plasma glucose post oral glucose challenge in mmol/L
Time Frame
3 years
Title
International physical activity questionnaire (IPAQ) score
Description
IPAQ score in MET minutes a week
Time Frame
3 years
Title
Metformin adherence
Description
Metformin adherence assessed by pill counts
Time Frame
Up to 30 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Singapore citizens or permanent residents Age between 18 and 64 Body mass index (BMI) ≥ 23.0 kg/m2 Pre-diabetes diagnosed based on: fasting plasma glucose 6.1 - 6.9 mmol/L (Impaired fasting glucose; IFG) and/or 2-hr plasma glucose in 75g oral glucose tolerance test (OGTT) 7.8 - 11.0 mmol/L (Impaired glucose tolerance; IGT) (Laboratory tests to be done within 6 months of enrolment) Exclusion Criteria: Individuals with diabetes mellitus Health conditions impeding participation in lifestyle change programme (e.g. active cancer, recent myocardial event within 6 months, heart failure, chronic kidney disease) Current pregnancy or breast feeding Treatment with medications known to alter glucose tolerance Known allergic reaction to metformin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yong Mong Bee
Organizational Affiliation
Singapore General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Singapore General Hospital
City
Singapore
ZIP/Postal Code
169608
Country
Singapore

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34362409
Citation
Yeung KF, Gandhi M, Lam AYR, Julianty S, Chia AYM, Tan GCS, Goh SY, Ho ETL, Koh AFY, Tan GSW, Shum EJW, Finkelstein EA, Jafar TH, Teoh YL, van Dam RM, Whitton C, Thumboo J, Bee YM. The Pre-Diabetes Interventions and Continued Tracking to Ease-out Diabetes (Pre-DICTED) program: study protocol for a randomized controlled trial. Trials. 2021 Aug 6;22(1):522. doi: 10.1186/s13063-021-05500-5.
Results Reference
derived

Learn more about this trial

The Pre-Diabetes Interventions and Continued Tracking to Ease-out Diabetes (Pre-DICTED) Program

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