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Web-based Dietary Intervention for Diabetic Patients

Dietary Intervention Among Patients With Type 2 Diabetes Mellitus: An e-Approach

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01246687
Acronym
myDIDeA
Enrollment
134
Registered
2010-11-23
Start date
2010-03-31
Completion date
2011-12-31
Last updated
2017-12-27

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

Conditions

Behavior, Diabetes Mellitus, Type 2, Intervention Studies

Brief summary

The Internet holds promise for a wide-scale promotion of dietary and lifestyle behavioural change. Website-delivered interventions have a potentially broad population reach as it is available 24 hours, and could be hosted by both government and non-governmental agencies. To date, there is no published study focused on dietary behaviour change in adults with Type 2 Diabetes Mellitus (T2DM) via a website-based system. myDIDeA was a 12-months two-armed randomised controlled trial conducted in three tertiary public hospitals in Klang Valley, Malaysia. The primary outcome was the Dietary Knowledge, Attitude and Behaviour (DKAB) score, while the secondary outcomes included the food intake, anthropometry measurements, blood pressure and resting heart rate, blood biomarkers and the Dietary Stages of Change (DSOC) score.

Detailed description

The study was designed according to the recommendations of the CONSORT statement for randomised trials of non-pharmacologic treatment. The study commenced in November 2009 after obtaining the ethical approvals from relevant authorities, and the trial has been registered with Clinicaltrials.gov (NCT01246687). After being screened for eligibility, 128 patients with Type 2 Diabetes Mellitus (T2DM) from the outpatient clinics at these hospitals were recruited into the study with informed consent. After the baseline data collection, the participants were randomised into the e-intervention (n=66) or the control (n=62) group. The e-intervention group received an intensive six-month dietary intervention through the study website, which was developed based on various established guidelines and recommendations but personalised according to the participants' DSOC, in addition to the usual standard treatment at the outpatient clinics. In contrast, the control group received the usual standard treatment given to patients with T2DM, and did not receive the website login information, or any reinforcement via e-mail or SMS. Data were collected at baseline, six months post-intervention and at 12 months follow-up. A structured and pre-tested questionnaire was used for this purpose. The anthropometry measurements, blood pressure and resting heart rate were measured at data collection. Details on the blood biomarkers were obtained from the hospital medical records. The statistical analysis revealed that myDIDeA was successful in improving overall DKAB score by improving the diabetes-related dietary knowledge and attitude of the participants. Besides, the intervention programme also have successfully improved the DSOC score of the intervention group, suggesting the participants were indeed making small but significant progress in changing their dietary behaviour. Improvement in the diet quality (improvement in vegetable intake and reduction in carbohydrate and protein intake), glycaemic control and total cholesterol have added credibility to this web-delivered intervention. The process evaluation of the study website revealed that on the average each participant logged in the website once a week and spent 11 minutes at the website per visit. The usability (facilitating conditions) scored the highest, while the acceptability (anxiety) scored the lowest.

Interventions

BEHAVIORALe-Intervention

Dietary educational programme developed using Transtheoretical Model of Change and delivered via a website specific for Type 2 Diabetes patients.

Sponsors

Monash University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Mentally sound men and women who are \> 18 years old. * Literate with a fair command of English and/or Malay languages. * Have access to the Internet at home, work or public place. * Willing to access the web portal at least once every fortnight. * Have been confirmed to have HbA1c of \>7%. * KAB score \< 50% at baseline.

Exclusion criteria

* Pregnant, lactating or intend to become pregnant during the study period. * Diagnosed with Type 1 Diabetes Mellitus (T1DM) or Gestational Diabetes Mellitus (GDM) * Weighing not more than 150% of the desired weight for height. * Any pre-existing condition compromising the quality of life or ability to participate according to protocol. * Have severe complications (chronic heart disease, cerebrovascular disease, diagnosed HIV/AIDS, cancer, emphysema, chronic liver or kidney disease) that would affect the subjects' ability to follow the tailored advice. * Enrolled in other clinical studies.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Dietary KAB Score at 6 monthsBaseline & 6 monthsDietary Knowledge, Attitude & Behaviour Score - assessed using 36-item questionnaire.
Change from Baseline in Dietary KAB Score at 12 monthsBaseline & 12 monthsDietary Knowledge, Attitude & Behaviour Score - assessed using 36-item questionnaire.

Secondary

MeasureTime frameDescription
Change from Baseline in dietary practices at 6 monthsBaseline & 6 monthsNutrient intake, dietary GI, supplement intake, food preparation & eating out habit
Change from Baseline in dietary practices at 12 monthsBaseline & 12 monthsNutrient intake, dietary GI, supplement intake, food preparation & eating out habit
Change from Baseline in anthropometric measurements at 6 monthsBaseline & 6 monthsBMI, body fat percentage, waist circumference
Change from Baseline in blood biomarkers at 12 monthsBaseline & 12 monthsHbA1c, fasting plasma glucose, lipid profile (data to be obtained from the medical records)
Change from Baseline in blood biomarkers at 6 monthsBaseline & 6 monthsHbA1c, fasting plasma glucose, lipid profile (data to be obtained from the medical records)
Change from Baseline in anthropometric measurements at 12 monthsBaseline & 12 monthsBMI, body fat percentage, waist circumference

Countries

Malaysia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026