Overweight and Obesity Clinical Trial
Official title:
A Randomised Controlled Trial of a Digital Therapy for Diabetes Prevention
NCT number | NCT03997656 |
Other study ID # | 2018/77 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | September 1, 2019 |
Est. completion date | July 1, 2021 |
The modern world revolves around technology; unsurprisingly companies are leveraging the expertise of the digital tech industry to aid in the prevention of chronic diseases. Among one of the most common chronic diseases in Malaysia is diabetes. Prevalence of diabetes in Malaysia has increased by more than two folds over the past two decades. Despite a growing number of tech products developments on diabetes prevention, a recent meta-analysis has found almost no evidence on digital therapy outside the developed world. Therefore, this study is needed to demonstrate the potential of digital therapy in preventing diabetes in Malaysia. The study design is a randomized controlled trial study conducted in Kuala Terengganu, Malaysia. The study will be conducted in two phases. The first phase will involve preparation of intervention modules and development of intervention mobile app. The second phase will involve validation and utilization of the digital therapy. We hope that this digital therapy program can make a significant difference in health outcomes, especially for diabetes. By giving precise regimes and daily monitoring, digital therapeutics can offer mountains of data that can potentially provide doctors unprecedented insights into patient behavior and create feedback or optimization loops for individual patients. Enabling patients to take greater control over managing their chronic illnesses and preventing disease progression could save billions of ringgits throughout the entire Malaysia healthcare system. By that, we hope this approach can be considered as a scalable solution to address national diabetes prevention efforts to target of improvement on diabetes prevalence to not more than 15% by 2025 and serve as a model for applying such services to other chronic diseases.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | July 1, 2021 |
Est. primary completion date | May 1, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - aged 18-65 years old - body mass index (BMI) of =23 kg/m2, - high risk for diabetes (diabetes risk test score =5 [22] or HbA1c of 38-44 mmol/mol or 5.6-6.2% - ownership of a smartphone (Android only) for communication defined as logging on at least once/day to the internet - being fluent in Malay or English languages and - had no contradictions to participate in weight management program or physical activity. Exclusion Criteria: - clinical history of diabetes or newly diagnosed diabetes at the time of screening where HbA1c level =45 mmol/mol or =6.3% - taking oral anti-diabetic agents - participating in a concurrent weight management program or interventional research protocol - on a prescribed medical diet, anti-obesity or diabetes therapy within the preceding 4 months - had clinical history of cardiovascular diseases occurred within the past 6 months - any form of cancers that require treatment - dementia or probable Alzheimer's disease - advanced arthritis - pregnant or within 6 weeks of having given birth or planning to become pregnant in the next 12 months - existing liver and renal disease and having hyperthyroidism - any mental health condition including eating disorder or alcohol/substance use - other causes which could interfere with participation (for examples physically disabled) |
Country | Name | City | State |
---|---|---|---|
Malaysia | University Sultan Zainal Abidin | Kuala Terengganu | Terengganu |
Lead Sponsor | Collaborator |
---|---|
Universiti Sultan Zainal Abidin |
Malaysia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | body weight | change of the initial body weight by 5% to 7% | 6-months and 12-months | |
Secondary | HbA1c level | HbA1c level will be tested using A1CNow+ test kit from a finger-stick blood samples collected in a capillary tube according to the manufacturer's procedure guidelines. To measure HbA1c with A1cNow+ test kit, the finger will be cleaned with alcohol swab, allowed to dry and then lanced with sterile lancet to obtain a drop of blood. A 5µl capillary blood sample will be collected and added to the sample dilution buffer. The diluted sample will be mixed and added to the monitoring using transfer pipette. Once the sample was applied, the monitor will begin the analyses. Digital results will be displayed in the display window after 5 minutes. The test result will be recorded for each participant. | 6-months and 12-months | |
Secondary | physical activity level | Physical activity (PA) will be assessed using translated and validated version of short-form International Physical Activity Questionnaire (IPAQ short form). It comprises of seven items that identify frequency and time spent on three specific types of physical activity (walking, moderate intensity activity, and vigorous intensity activity) during the past seven days. The Metabolic Equivalent (MET) values will be measured. The subjects' total physical activity (MET-minutes/week) will be calculated by summing up the walking, moderate and vigorous intensity activity scores. Subjects will be categorised as "active" if they achieved =600 MET-minutes/week, "moderately active" if they achieved =150 MET-minutes/week and "inactive" if they achieved <150 MET-minutes/week. | 6-months and 12-months | |
Secondary | dietary intake | The dietary intake status of the participants will be assessed from their food diary record from the app and the diary for intervention and control participants respectively. Participants will be asked to record their dietary intake for three days (two weekdays and one weekend) and the average measurement will be taken. A dietary analysis software, Nutritionist Pro Inc. will be used for energy and nutrient analysis. | 6-months and 12-months | |
Secondary | health-related quality of life | HRQoL will be assessed using translated and validated version of SF-36 health survey questionnaire. It comprises of 36 items which measure eight health domains which are physical functioning (PF), role-physical (RP), bodily pain (BP), general health (GH), vitality (VT), social functioning (SF), role-emotion (RE) and mental health (MH). The eight domains will be scored from 0 to 100 indicating worst to best possible health. All the scores will be further summarised into the Physical Component Summary score (PCS) and the Mental Component Summary score (MCS). | 6-months and 12-months |
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