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A Community-based Weight Loss Programme for Chinese Overweight Adults With Pre-diabetes

Primary Purpose

Pre-diabetes

Status
Active
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
group-based lifestyle intervention
Minimal intervention (SMS intervention)
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pre-diabetes focused on measuring Diabetes prevention, Pre-diabetes, Weight loss, Cardio-metabolic risks, Obesity, Lifestyle intervention, Community-based

Eligibility Criteria

30 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • aged 30 to 65 years
  • overweight (BMI ≥ 23kg/m2) or obese (BMI ≥ 25 kg/m2)
  • with at least one blood test result showing IGT (7.8-11.0 mmol/L after a two-hour glucose tolerance test), IFG (fasting glucose 5.6 - 6.9 mmol/L) or impaired HbA1c 5.7% - 6.4%
  • have a mobile phone
  • able to read Chinese and speak Cantonese.

Exclusion Criteria:

  • with current or clinical history of T2DM, or with co-morbid conditions that may limit participation in the study, such as recent history of an acute cardiovascular event, uncontrolled hypertension, cancer or major psychiatric or cognitive problems
  • already participating in a weight loss programme
  • receiving drug treatment for pre-diabetes (e.g. Metformin) or long-term use of medications known to influence glucose metabolism (e.g. corticosteroids)

Sites / Locations

  • The University of Hong Kong

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Community-based lifestyle intervention

Minimal intervention (SMS intervention)

Arm Description

Participants will attend 7 community-based group intervention sessions plus 2 individual face-to-face dietician consultation sessions during the first 6 months, followed by a 6-month maintenance phase which they will receive monthly phone support from the research team.

Participants will receive one SMS per month during the first 6 months, followed by a 6-month maintenance phase which participants will receive one SMS every 2 months.

Outcomes

Primary Outcome Measures

Percent weight change
% weight change from baseline

Secondary Outcome Measures

Homeostatic Model Assessment of Insulin Resistance (HOMA-IR)
Estimated from fasting insulin and fasting glucose, [fasting insulin (uU/mL)*fasting glucose(mmol/L)]/22.5
Fasting insulin
Fasting insulin
Fasting blood glucose (FG)
Fasting blood glucose
Haemoglobin A1C (HbA1C)
HbA1C
Systolic and diastolic blood pressure (SBP, DBP)
measured by automatic BP monitor
Blood lipid profile
fasting blood for total cholesterol, HDL, LDL and triglycerides
Diabetes status
Oral glucose tolerance test
Physical activity
International physical activity questionnaire short form (IPAQ, Chinese version). A validated 6-item questionnaire to assess the frequency and duration of vigorous intensity activity, moderate intensity activity, and walking. The questionnaire will be scored using established methods (www.ipaq.ki.se). Data will be summarized to report physical activity in categories: High-active group Vigorous-intensity activity on ≥ 3 days and accumulating ≥1500 MET-minutes/week OR ≥7 days of any combination of walking, moderate-intensity or vigorous intensity activities achieving ≥3000 MET-minutes/week Moderate-active group ≥3 days of vigorous activity of ≥20 minutes/day OR ≥5 days of moderate-intensity activity or walking of ≥30 minutes/day OR ≥5 days of any combination of walking, moderate-intensity or vigorous intensity activities achieving ≥600 MET-min/week. Low-active/inactive group Individuals who do not meet criteria for high- and moderate-active
Dietary intake
24 hour recalls
Health-related quality of life (HRQOL)
12-item Short Form Survey (SF12 Chinese version). It is a validated scale which provides two summary measures. Physical and Mental Health Composite Scores (PCS & MCS) will be computed using the scores of 12 questions and range from 0 to 100. Higher scores represent better health.
Carotid artery intima-media thickness (cIMT)
High-resolution B-mode ultrasonography

Full Information

First Posted
July 13, 2018
Last Updated
October 16, 2021
Sponsor
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT03609697
Brief Title
A Community-based Weight Loss Programme for Chinese Overweight Adults With Pre-diabetes
Official Title
Effects of a Community-based Weight Loss Programme Targetting Chinese Overweight Adults With Pre-diabetes: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 10, 2018 (Actual)
Primary Completion Date
May 31, 2022 (Anticipated)
Study Completion Date
May 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong

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
Type 2 diabetes (T2DM) is a serious chronic condition and one of the world's fastest growing health problems. The onset of T2DM is gradual, with most individuals progressing through a state of pre-diabetes. Pre-diabetes is a prevalent and potentially reversible condition, which provides an important window of opportunity for the prevention of T2DM and its complications. This project aims to translate the evidence-based diabetes prevention strategies into a community setting to reduce diabetes risks in Hong Kong Chinese people with pre-diabetes .
Detailed Description
Type 2 diabetes (T2DM) is a major non-communicable disease and one of the world's fastest growing health problem. It is associated with significant morbidity, including increased risk of heart disease and stroke, hypertension, retinopathy and blindness, renal failure and leg amputation, which place an enormous burden on individuals, society and the healthcare system. The T2DM trend in Hong Kong mirrors the global trend. It is a major cause of mortality and morbidity with approximately 700,000 people diagnosed with diabetes, representing 10% of Hong Kong's total population. T2DM is a non-reversible, yet a preventable condition. The onset of T2DM is gradual, with most individuals progressing through a state of pre-diabetes. People with pre-diabetes, defined as having impaired fasting glucose (IFG), impaired glucose tolerance (IGT) or elevated glycated haemoglobulin (HbA1C) , are at increased risk of developing T2DM and its associated complications, such as heart diseases and retinopathy, which can develop even in the absence of progression to overt T2DM. Hence, it is essential that people with pre-diabetes are targeted for early intervention to prevent T2DM and related complications. International clinical trials demonstrated that lifestyle interventions targeting at least 5% weight loss in individuals with pre-diabetes can be cost-effective in preventing T2DM. Lifestyle intervention (which includes diet, physical activity and behavioural modification components) and self-management of pre-diabetes has been listed as an effective means of decreasing the incidence of T2DM in the international guidelines on management of pre-diabetes. The aim of this study is to translate preventive research into effective community-based intervention by setting up a culturally appropriate lifestyle intervention programme for the prevention of T2DM in Hong Kong Chinese adults with pre-diabetes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pre-diabetes
Keywords
Diabetes prevention, Pre-diabetes, Weight loss, Cardio-metabolic risks, Obesity, Lifestyle intervention, Community-based

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
It is a 12-month 2-arm randomised controlled trial, RCT (the lifestyle intervention group and the SMS intervention group) with a 3 year follow up. The programme will proceed in two phases: the intensive intervention phase (0-6 months) and the maintenance phase (7-12 months). During the intensive intervention phase, participants in the lifestyle intervention group will attend 7 group-based interventions plus two sessions of individual face-to-face dietician consultation. During the maintenance phase, participants will receive monthly phone call from the research team. The SMS intervention group will receive regular SMS during both the intensive intervention and the maintenance phases.
Masking
Outcomes Assessor
Masking Description
All outcome assessors will be blinded to group allocation
Allocation
Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Community-based lifestyle intervention
Arm Type
Experimental
Arm Description
Participants will attend 7 community-based group intervention sessions plus 2 individual face-to-face dietician consultation sessions during the first 6 months, followed by a 6-month maintenance phase which they will receive monthly phone support from the research team.
Arm Title
Minimal intervention (SMS intervention)
Arm Type
Other
Arm Description
Participants will receive one SMS per month during the first 6 months, followed by a 6-month maintenance phase which participants will receive one SMS every 2 months.
Intervention Type
Behavioral
Intervention Name(s)
group-based lifestyle intervention
Other Intervention Name(s)
individual dietitian consultation, Telephone support, community-based intervention
Intervention Description
Involve education about pre-diabetes self-management, weight loss, behavioural modification skills, nutrition and physical activity.
Intervention Type
Behavioral
Intervention Name(s)
Minimal intervention (SMS intervention)
Intervention Description
Text message related to general information about T2DM, pre-diabetes, and lifestyle modification.
Primary Outcome Measure Information:
Title
Percent weight change
Description
% weight change from baseline
Time Frame
% weight change from baseline at 6-month and 12-months
Secondary Outcome Measure Information:
Title
Homeostatic Model Assessment of Insulin Resistance (HOMA-IR)
Description
Estimated from fasting insulin and fasting glucose, [fasting insulin (uU/mL)*fasting glucose(mmol/L)]/22.5
Time Frame
Changes from baseline insulin sensitivity at 6-month and 12-months
Title
Fasting insulin
Description
Fasting insulin
Time Frame
Changes from baseline fasting insulin at 6-month and 12-months
Title
Fasting blood glucose (FG)
Description
Fasting blood glucose
Time Frame
Changes from baseline FG at 6-month and 12-months
Title
Haemoglobin A1C (HbA1C)
Description
HbA1C
Time Frame
Changes from baseline HbA1Cat 6-month and 12-months
Title
Systolic and diastolic blood pressure (SBP, DBP)
Description
measured by automatic BP monitor
Time Frame
Changes from baseline SBP and DBP at 6-month and 12-months
Title
Blood lipid profile
Description
fasting blood for total cholesterol, HDL, LDL and triglycerides
Time Frame
Changes from baseline blood lipid to 6-month and 12-months
Title
Diabetes status
Description
Oral glucose tolerance test
Time Frame
6-month and 12-months follow-up
Title
Physical activity
Description
International physical activity questionnaire short form (IPAQ, Chinese version). A validated 6-item questionnaire to assess the frequency and duration of vigorous intensity activity, moderate intensity activity, and walking. The questionnaire will be scored using established methods (www.ipaq.ki.se). Data will be summarized to report physical activity in categories: High-active group Vigorous-intensity activity on ≥ 3 days and accumulating ≥1500 MET-minutes/week OR ≥7 days of any combination of walking, moderate-intensity or vigorous intensity activities achieving ≥3000 MET-minutes/week Moderate-active group ≥3 days of vigorous activity of ≥20 minutes/day OR ≥5 days of moderate-intensity activity or walking of ≥30 minutes/day OR ≥5 days of any combination of walking, moderate-intensity or vigorous intensity activities achieving ≥600 MET-min/week. Low-active/inactive group Individuals who do not meet criteria for high- and moderate-active
Time Frame
Change in levels of physical activity from baseline to 6-month and 12-months
Title
Dietary intake
Description
24 hour recalls
Time Frame
Changes in dietary intake from baseline to 6-month and 12-months
Title
Health-related quality of life (HRQOL)
Description
12-item Short Form Survey (SF12 Chinese version). It is a validated scale which provides two summary measures. Physical and Mental Health Composite Scores (PCS & MCS) will be computed using the scores of 12 questions and range from 0 to 100. Higher scores represent better health.
Time Frame
Changes in HRQOL from baseline to 6-month and 12-months
Title
Carotid artery intima-media thickness (cIMT)
Description
High-resolution B-mode ultrasonography
Time Frame
Change in cIMT from baseline to 6-month and 12-months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: aged 30 to 65 years overweight (BMI ≥ 23kg/m2) or obese (BMI ≥ 25 kg/m2) with at least one blood test result showing IGT (7.8-11.0 mmol/L after a two-hour glucose tolerance test), IFG (fasting glucose 5.6 - 6.9 mmol/L) or impaired HbA1c 5.7% - 6.4% have a mobile phone able to read Chinese and speak Cantonese. Exclusion Criteria: with current or clinical history of T2DM, or with co-morbid conditions that may limit participation in the study, such as recent history of an acute cardiovascular event, uncontrolled hypertension, cancer or major psychiatric or cognitive problems already participating in a weight loss programme receiving drug treatment for pre-diabetes (e.g. Metformin) or long-term use of medications known to influence glucose metabolism (e.g. corticosteroids)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Mandy Ho
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Hong Kong
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to make individual participant data available to other researchers.
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A Community-based Weight Loss Programme for Chinese Overweight Adults With Pre-diabetes

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