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

Effects of a Community-based Weight Loss Programme Targetting Chinese Overweight Adults With Pre-diabetes: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03609697
Enrollment
180
Registered
2018-08-01
Start date
2018-08-10
Completion date
2024-05-31
Last updated
2021-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pre-diabetes

Keywords

Diabetes prevention, Pre-diabetes, Weight loss, Cardio-metabolic risks, Obesity, Lifestyle intervention, Community-based

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.

Interventions

Involve education about pre-diabetes self-management, weight loss, behavioural modification skills, nutrition and physical activity.

BEHAVIORALMinimal intervention (SMS intervention)

Text message related to general information about T2DM, pre-diabetes, and lifestyle modification.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

All outcome assessors will be blinded to group allocation

Intervention 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.

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Percent weight change% weight change from baseline at 6-month and 12-months% weight change from baseline

Secondary

MeasureTime frameDescription
Homeostatic Model Assessment of Insulin Resistance (HOMA-IR)Changes from baseline insulin sensitivity at 6-month and 12-monthsEstimated from fasting insulin and fasting glucose, \[fasting insulin (uU/mL)\*fasting glucose(mmol/L)\]/22.5
Fasting insulinChanges from baseline fasting insulin at 6-month and 12-monthsFasting insulin
Fasting blood glucose (FG)Changes from baseline FG at 6-month and 12-monthsFasting blood glucose
Haemoglobin A1C (HbA1C)Changes from baseline HbA1Cat 6-month and 12-monthsHbA1C
Blood lipid profileChanges from baseline blood lipid to 6-month and 12-monthsfasting blood for total cholesterol, HDL, LDL and triglycerides
Systolic and diastolic blood pressure (SBP, DBP)Changes from baseline SBP and DBP at 6-month and 12-monthsmeasured by automatic BP monitor
Physical activityChange in levels of physical activity from baseline to 6-month and 12-monthsInternational 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: 1. 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 2. 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. 3. Low-active/inactive group Individuals who do not meet criteria for high- and moderate-active
Dietary intakeChanges in dietary intake from baseline to 6-month and 12-months24 hour recalls
Health-related quality of life (HRQOL)Changes in HRQOL from baseline to 6-month and 12-months12-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)Change in cIMT from baseline to 6-month and 12-monthsHigh-resolution B-mode ultrasonography
Diabetes status6-month and 12-months follow-upOral glucose tolerance test

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026