- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04217759
Healthy Lifestyle Intervention on Diabetes Risk Reduction Among Bruneian Young Adults
Effectiveness of Healthy Lifestyle Intervention on Diabetes Risk Reduction Among Bruneian Young Adults: a Randomised Controlled Trial
The general research question posed was 'How effective is a healthy lifestyle intervention using behavioural change strategies in the prevention of Type 2 Diabetes Mellitus (T2DM)?'.
The main aim was to assess the effectiveness of a healthy lifestyle intervention implemented for 12 weeks via face-to-face group sessions and by using social media tools (Facebook and WhatsApp) for young adults at risk of T2DM.
The hypothesis was that this healthy lifestyle intervention may be effective in terms of initiating an increased physical activity (PA) level and a healthy balanced dietary intake resulting in improvements of other T2DM risk factors at 12 weeks.
Study Overview
Status
Intervention / Treatment
Detailed Description
The specific research question posed was 'Is a healthy lifestyle intervention using Social Cognitive Theory (SCT)-based PA and dietary strategies implemented for 12 weeks through face-to-face group sessions and social media tools effective in the initiation and maintenance of increased PA level and healthy balanced dietary intake, resulting in improvements of T2DM risk score, anthropometrics, metabolic parameters and SCT-related psychosocial factors among Bruneian young adults at risk of T2DM?'.
Study design was two-arm parallel, stratified with simple randomisation, and assessor-blinded randomised controlled trial. Participants were randomly allocated into intervention group and control group. Participants were students and alumni of Universiti Brunei Darussalam and Universiti Teknologi Brunei who were overweight-obese at risk of T2DM with a mean age of 23.1 (2.48) years old. Intervention group went through a healthy lifestyle intervention using evidence-based SCT strategies emphasising on PA and diet for 12 weeks, while the control group only received leaflets on healthy lifestyle with no further guidance. Outcomes measured were changes from baseline at week 0 to post-intervention at week 13 between intervention and control groups. Outcomes were changes in diabetes risk score, anthropometrics, metabolic parameters, PA, dietary intake and SCT-related psychosocial factors, with repeated-measures ANOVA as the main analysis.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Bandar Seri Begawan
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Brunei, Bandar Seri Begawan, Brunei Darussalam, BE1410
- PAPRSB Institute of Health Sciences, Universiti Brunei Darussalam
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Bruneian including permanent residents
- BMI from 25.00 to 39.99 kg/m2
- American Diabetes Association (ADA) diabetes risk score of at least 3 and maximum score of 8
- Mentally and physically fit with no chronic conditions
- Without medical conditions that could influence glucose metabolism and insulin resistance
- Answered 'No' to all 6 questions in questionnaire-based pre-exercise risk assessment
- Not actively participating in other healthy lifestyle programmes
- Had access to computer or mobile phone with Internet
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Intervention group
Intervention group went through a healthy lifestyle intervention using evidence-based SCT strategies emphasising on PA and diet for 12 weeks via face-to-face sessions and social media tools (Facebook and WhatsApp)
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The main goal was to provide knowledge and skills for targeted population in order for them to adapt healthy lifestyle throughout their life. At the end of intervention, participants were expected to be fully equipped with necessary knowledge and fundamental skills in adapting and maintaining healthy lifestyle throughout their life. Gradual improvements were emphasised and at least 5% loss of initial body weight was expected, aiming for at least 0.5% loss in the first month. It was divided into three phases (preparation, implementation, maintenance) focusing on PA and diet, in which self-efficacy enhancement and self-regulatory skills were emphasised during the first month of intervention.
Other Names:
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No Intervention: Control group
Control group only received leaflets on healthy lifestyle with no further guidance.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in diabetes risk score from week 0 to week 13
Time Frame: 12 weeks
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Using Finnish Diabetes Risk Score (FINDRISC) questionnaire, with minimum score of 0 and maximum score of 22. Score less than 7 as low risk, 7 to 11 as slightly elevated, 12 to 14 as moderate risk, 15 to 20 as high risk and more than 20 as very high risk.
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12 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in weight (kg)
Time Frame: 12 weeks
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Using digital weighing scale
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12 weeks
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Change in weight (%)
Time Frame: 12 weeks
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Using digital weighing scale
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12 weeks
|
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Height in cm
Time Frame: At baseline
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Using digital weighing scale
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At baseline
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Change in body mass index (BMI) (kg/m2)
Time Frame: 12 weeks
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Calculated with weight and height
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12 weeks
|
|
Change in waist circumference (WC) (cm)
Time Frame: 12 weeks
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Measured at the midpoint between the lower border of the ribcage and iliac crest with tape measure
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12 weeks
|
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Change in hip circumference (HC) (cm)
Time Frame: 12 weeks
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Measured at the largest portion of the buttocks with tape measure
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12 weeks
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Change in waist-to-hip ratio (WHR)
Time Frame: 12 weeks
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Calculated with WC and HC
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12 weeks
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Change in fasting blood glucose (FBG) (mmol/l)
Time Frame: 12 weeks
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With finger-pricking and AccuTrend Plus System blood analyses
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12 weeks
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Change in fasting blood total cholesterol (TC) (mmol/l)
Time Frame: 12 weeks
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With finger-pricking and AccuTrend Plus System blood analyses
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12 weeks
|
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Change in fasting blood triglycerides (TG) (mmol/l)
Time Frame: 12 weeks
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With finger-pricking and AccuTrend Plus System blood analyses
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12 weeks
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Change in systolic blood pressure (SBP) (mmHg)
Time Frame: 12 weeks
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Using OMRON automated blood pressure monitor
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12 weeks
|
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Change in diastolic blood pressure (DBP) (mmHg)
Time Frame: 12 weeks
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Using OMRON automated blood pressure monitor
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12 weeks
|
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Change in resting heart rate (pulse/min)
Time Frame: 12 weeks
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Using OMRON automated blood pressure monitor
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12 weeks
|
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Change in vigorous PA metabolic task (MET) (min/week)
Time Frame: 12 weeks
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Using short-form international PA questionnaire (SF-IPAQ)
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12 weeks
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Change in moderate PA MET (min/week)
Time Frame: 12 weeks
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Using SF-IPAQ
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12 weeks
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Change in walking MET (min/week)
Time Frame: 12 weeks
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Using SF-IPAQ
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12 weeks
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Change in total PA MET (min/week)
Time Frame: 12 weeks
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Using SF-IPAQ
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12 weeks
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Change in sitting time (hrs/day)
Time Frame: 12 weeks
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Using SF-IPAQ
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12 weeks
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Change in intake of carbohydrates (servings/day)
Time Frame: 12 weeks
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Using 4-day dietary record
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12 weeks
|
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Change in intake of protein (servings/day)
Time Frame: 12 weeks
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Using 4-day dietary record
|
12 weeks
|
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Change in intake of fruits (servings/day)
Time Frame: 12 weeks
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Using 4-day dietary record
|
12 weeks
|
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Change in Intake of vegetables (servings/day)
Time Frame: 12 weeks
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Using 4-day dietary record
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12 weeks
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Change in intake of water in (litres/day)
Time Frame: 12 weeks
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Using 4-day dietary record
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12 weeks
|
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Change in motivation score
Time Frame: 12 weeks
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Using University of Rhode Island Change Assessment (URICA) with minimum score of -2 and maximum score of 14.
The higher the score, the higher the motivation.
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12 weeks
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Change in social support (diet) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate better support for eating healthy.
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12 weeks
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Change in social support (PA) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate better support for exercising
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12 weeks
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Change in overcoming barriers (PA) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate more capabilities to overcome barriers towards exercising
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12 weeks
|
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Change in moral disengagement (diet) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate lack of control in eating
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12 weeks
|
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Change in outcome expectations (diet) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate more positive expectations for dieting
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12 weeks
|
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Change in outcome expectations (PA) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate more positive expectations for exercising
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12 weeks
|
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Change in emotional coping (PA) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate better emotional coping by exercising
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12 weeks
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Change in self-efficacy (PA) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate better confidence in exercising
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12 weeks
|
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Facilitation (PA) score
Time Frame: 12 weeks
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Using social cognitive theory (SCT) constructs scale with minimum score of 1 and maximum score of 4. Higher scores indicate better access to facilities and equipment for exercising
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12 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Alifah Nur'ain Haji Mat Rasil, University Brunei Darussalam
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- UBDIHS/13H0621
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
All collected data was available only within the research team which consisted of supervisors only:
- Dr Nik Tuah (main supervisor)
- Dr Mas Rina Wati Hamid (co-supervisor)
- Assoc Prof Dr Ayub Sadiq (co-supervisor)
IPD Sharing Time Frame
IPD Sharing Access Criteria
Research team
- Dr Alifah Nur'ain Haji Mat Rasil (principal investigator)
- Dr Nik Tuah (main supervisor)
- Dr Mas Rina Wati Hamid (co-supervisor)
- Assoc Prof Dr Ayub Sadiq (co-supervisor)
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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