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Status unknownNCT05203575Updated Sep 28, 2022

Building a Behavioural Intervention Programme to Improve Self-Management of Diabetes

An interventional study of Fast-forwarding in Cycle 1 and Goal-Setting plus Weekly Nudge in Cycle 1 in Diabetes, sponsored by National University of Singapore. Status unknown at 1 site in Singapore. Open to participants aged 21 Years to 70 Years. Per ClinicalTrials.gov, last updated 2022-09-28.

Sponsored by National University of Singapore · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Sep 2022), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
225
Allocation
Randomized
Ages
21 Years to 70 Years
Sex
All
01

Study summary

Effective control of diabetes requires patients to change their daily behaviour. The investigators propose an intervention programme for behavioural change with two components, targeting motivation and implementation. The motivation component raises the salience of probable patient-specific detrimental future outcomes by 'fast-forwarding' awareness of these outcomes to the present. The implementation component helps patients to set goals and to act based on weekly tips. A factorial design will be used to establish the necessity and sufficiency of the two components on changing mind and guiding behaviour to improve blood glucose level. Individual-level measures of psychological, physical and medical conditions will be shown to drive the heterogenous responses to the two components. Intervention is expanded into two cycles with crossover design to demonstrate how the individual-level measures drive the wear-off, built-up and persistence of the two components. The results of this two-component programme will serve as a basis for systematic synthesis of component-level effectiveness in behavioural intervention research.

Read the detailed description

This behavioural-change-intervention programme will be an online 'single-centre' outpatient randomized controlled trial (RCT) with ten study arms. It will be a two-component intervention consisting of a motivation component of fast-forwarding and an implementation component of goal-setting and weekly nudges. The field intervention will be structured into a two-cycle four-treatment crossover design with four treatment conditions in the first cycle and crossing-over into eight treatment conditions (including one control condition) in the second cycle. In addition to the control group in the study, a group of patients from the Singapore Health Services (SingHealth) Diabetes Registry dataset will be identified using propensity scoring to serve as a 'match-pair' for each study participant. The electronic medical record of this match-pair will provide an additional benchmark of biological measure in addition to that provided by the control group.

The field study will run for 34 weeks, in two cycles of 14 weeks each, with a 2-week transition period between the two cycles. There will also be a 2-week baseline period in which baseline measurements will be taken before the first cycle begins and a 2-week debriefing period where the final measurement will be taken after the end of the second cycle. Measurements will be taken three times: once before Cycle 1 (as the baseline), once between Cycles 1 and 2, and once at the end of Cycle 2. Participants who are assigned to the motivation component of fast-forwarding will receive fast-forwarding immediately after the measurement session and before the cycle. The participants who are randomly assigned to treatment conditions, including the implementation component, will receive a weekly nudge programme with each 14-week cycle. All participants will have access to the resources used to generate the 14-week cycles.

The investigators will measure the following: (i) physiological and medical information related to the progression of diabetes; (ii) diet quality and exercise level; (iii) psychological reactions towards diabetes management; (iv) behavioural change readiness and commitment; and (v) lifestyle (smoking, alcohol consumption, and sleep quality).

02

Conditions studied

  • Diabetes

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03

In context

Diabetes Mellitus

11,090 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 225 is above the median of 80 across 8,491 interventional studies indexed under Diabetes Mellitus.

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Lead sponsor

National University of Singapore is the lead sponsor of 212 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age between 21-70
  • Has type 2 diabetes
  • Comfortable communicating English
  • Uses smartphone app WhatsApp

Exclusion criteria

Exclusion Criteria:

  • Participants with diagnoses of mental health illnesses
  • Participants who are unable to provide informed consent
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
225 participants (actual)

Study arms

  • No intervention
    Control

    Control condition

  • Experimental
    Weekly nudge in Cycle 2

    Weekly nudge intervention in Cycle 2

    Behavioral: Goal-Setting plus Weekly Nudge in Cycle 2

  • Experimental
    Fast-forwarding

    Fast-forwarding interventions in both Cycles

    Behavioral: Fast-forwarding in Cycle 1 · Behavioral: Fast-forwarding in Cycle 2

  • Experimental
    Fast-forwarding with weekly nudge in Cycle 2

    Fast-forwarding interventions in both Cycles, plus weekly nudge intervention in Cycle 2

    Behavioral: Fast-forwarding in Cycle 1 · Behavioral: Fast-forwarding in Cycle 2 · Behavioral: Goal-Setting plus Weekly Nudge in Cycle 2

  • Experimental
    Weekly nudge in Cycle 1

    Weekly nudge intervention in Cycle 1

    Behavioral: Goal-Setting plus Weekly Nudge in Cycle 1

  • Experimental
    Weekly nudge

    Weekly nudge interventions in both Cycles

    Behavioral: Goal-Setting plus Weekly Nudge in Cycle 1 · Behavioral: Goal-Setting plus Weekly Nudge in Cycle 2

  • Experimental
    Fast-forwarding with weekly nudge in Cycle 1

    Fast-forwarding interventions in both Cycles, plus weekly nudge intervention in Cycle 1

    Behavioral: Fast-forwarding in Cycle 1 · Behavioral: Goal-Setting plus Weekly Nudge in Cycle 1 · Behavioral: Fast-forwarding in Cycle 2

  • Experimental
    Full intervention

    All interventions applied in all Cycles

    Behavioral: Fast-forwarding in Cycle 1 · Behavioral: Goal-Setting plus Weekly Nudge in Cycle 1 · Behavioral: Fast-forwarding in Cycle 2 · Behavioral: Goal-Setting plus Weekly Nudge in Cycle 2

  • Experimental
    Fast-forwarding in Cycle 1

    Fast-forwarding intervention in Cycle 1

    Behavioral: Fast-forwarding in Cycle 1

  • Experimental
    Full in Cycle 1

    Fast-forwarding and weekly nudge interventions in Cycle 1

    Behavioral: Fast-forwarding in Cycle 1 · Behavioral: Goal-Setting plus Weekly Nudge in Cycle 1

Interventions

  • BehavioralFast-forwarding in Cycle 1

    The fast-forwarding intervention will consist of a projection of future risk of co-morbidities. A visual projection model will be built using archival data available through the Singapore Diabetes Registry. The projection model will use the current profile of the participant to calculate a risk profile for the participant's potential complications and co-morbidities, which will be presented as a pie chart. The tool will also present alternative scenarios to the participant and visualize how the likelihood of complications or co-morbidities would decrease or increases if his/her habits changed. This will provide the motivational aspect of the intervention. This intervention takes place during Cycle 1 (first 14 weeks).

  • BehavioralGoal-Setting plus Weekly Nudge in Cycle 1

    The procedure for goal-setting will start with the participant receiving a list of possible goals. The moderator will go through the list with the participant to identify which goals the participant is comfortable with and could reasonably achieve, and to tick off those goals that the participant has already achieved. The participants will choose their own goals. In each subsequent week, the moderator will check-in with the participant and tick off the goal(s) that have been achieved. Chat groups of 10-15 people will be formed to administer the weekly nudge. The participants will be encouraged to introduce themselves and to interact with each other during each the chat session. Every week for the following 14 weeks, the moderator will post diabetes-related content on the WhatsApp chat group and introduce topics of interest according to a planned schedule. This intervention takes place during Cycle 1 (first 14 weeks).

  • BehavioralFast-forwarding in Cycle 2

    The fast-forwarding intervention will consist of a projection of future risk of co-morbidities. A visual projection model will be built using archival data available through the Singapore Diabetes Registry. The projection model will use the current profile of the participant to calculate a risk profile for the participant's potential complications and co-morbidities, which will be presented as a pie chart. The tool will also present alternative scenarios to the participant and visualize how the likelihood of complications or co-morbidities would decrease or increases if his/her habits changed. This will provide the motivational aspect of the intervention. This intervention takes place during Cycle 2 (second 14 weeks).

  • BehavioralGoal-Setting plus Weekly Nudge in Cycle 2

    The procedure for goal-setting will start with the participant receiving a list of possible goals. The moderator will go through the list with the participant to identify which goals the participant is comfortable with and could reasonably achieve, and to tick off those goals that the participant has already achieved. The participants will choose their own goals. In each subsequent week, the moderator will check-in with the participant and tick off the goal(s) that have been achieved. Chat groups of 10-15 people will be formed to administer the weekly nudge. The participants will be encouraged to introduce themselves and to interact with each other during each the chat session. Every week for the following 14 weeks, the moderator will post diabetes-related content on the WhatsApp chat group and introduce topics of interest according to a planned schedule. This intervention takes place during Cycle 2 (second 14 weeks).

06

What researchers measure

Primary outcomes

  1. HbA1c after Cycle 1

    Results from HbA1c test

    Time frame: Measured between Weeks 17-18

  2. HbA1c after Cycle 2

    Results from HbA1c test

    Time frame: Measured between Weeks 33-34

Secondary outcomes

  1. Diet quality after Cycle 1

    Diet quality will be measured using the well-validated Food Frequency Questionnaire

    Time frame: Measured between Weeks 17-18

  2. Diet quality after Cycle 2

    Diet quality will be measured using the well-validated Food Frequency Questionnaire

    Time frame: Measured between Weeks 33-34

  3. Exercise levels after Cycle 1

    Exercise level will be assessed based on the Global Physical Activity Questionnaire (GPAQ) developed by the World Health Organization in 2002 for chronic disease risk-factor surveillance

    Time frame: Measured between Weeks 17-18

  4. Exercise levels after Cycle 2

    Exercise level will be assessed based on the Global Physical Activity Questionnaire (GPAQ) developed by the World Health Organization in 2002 for chronic disease risk-factor surveillance

    Time frame: Measured between Weeks 33-34

  5. Attitudes towards diabetes management after Cycle 1

    The participants' psychological reactions towards diabetes treatment will be captured using three main groups of questionnaires. Their general attitudes towards diabetes will be measured using the Diabetes Attitude Survey developed and validated by the University of Michigan Diabetes Research and Training Center (MDRC). The investigators will measure how strongly the patients feel empowered to cope with and manage diabetes, which is a crucial outcome of DSME. Empowerment will be captured using the Diabetes Empowerment Scale (DES) developed by the MDRC. To gain insight into the psychological processes through which fast-forwarding and implementation influence health outcomes, the investigators will measure attitudes towards perceived barriers to diet adherence, exercise, and monitoring, using the respective subscales of the Diabetes Care Profile developed by MDTC

    Time frame: Measured between Weeks 17-18

  6. Attitudes towards diabetes management after Cycle 2

    The participants' psychological reactions towards diabetes treatment will be captured using three main groups of questionnaires. Their general attitudes towards diabetes will be measured using the Diabetes Attitude Survey developed and validated by the University of Michigan Diabetes Research and Training Center (MDRC). The investigators will measure how strongly the patients feel empowered to cope with and manage diabetes, which is a crucial outcome of DSME. Empowerment will be captured using the Diabetes Empowerment Scale (DES) developed by the MDRC. To gain insight into the psychological processes through which fast-forwarding and implementation influence health outcomes, the investigators will measure attitudes towards perceived barriers to diet adherence, exercise, and monitoring, using the respective subscales of the Diabetes Care Profile developed by MDTC

    Time frame: Measured between Weeks 33-34

  7. Readiness for behavioral change after Cycle 1

    To assess readiness for behavioural change, the investigators will ask the participants to indicate their commitment to make changes to their diet and physical activity. Specifically, the investigators will ask them to name a food that they have been told to eat less of, and to indicate how many times they are willing to cut back on the food. Similarly, the investigators will ask the participants to indicate how much time per week they are willing to exercise to avoid future complications arising from their diabetes

    Time frame: Measured between Weeks 17-18

  8. Readiness for behavioral change after Cycle 2

    To assess readiness for behavioural change, the investigators will ask the participants to indicate their commitment to make changes to their diet and physical activity. Specifically, the investigators will ask them to name a food that they have been told to eat less of, and to indicate how many times they are willing to cut back on the food. Similarly, the investigators will ask the participants to indicate how much time per week they are willing to exercise to avoid future complications arising from their diabetes

    Time frame: Measured between Weeks 33-34

  9. Smoking status after Cycle 1

    Self-reported smoking status

    Time frame: Measured between Weeks 17-18

  10. Smoking status after Cycle 2

    Self-reported smoking status

    Time frame: Measured between Weeks 33-34

  11. Level of alcohol consumption after Cycle 1

    Self-reported frequency of alcohol consumption

    Time frame: Measured between Weeks 17-18

  12. Level of alcohol consumption after Cycle 2

    Self-reported frequency of alcohol consumption

    Time frame: Measured between Weeks 33-34

  13. Sleep quality after Cycle 1

    Self-reported quality of sleep

    Time frame: Measured between Weeks 17-18

  14. Sleep quality after Cycle 2

    Self-reported quality of sleep

    Time frame: Measured between Weeks 33-34

07

Study locations

1 site
  • National University of Singapore
    Singapore, Singapore
08

References and documents

Individual participant data

Plan to share: Yes — Investigators will not be storing or sharing any personal identifiers. All individual level data will be anonymized, and only anonymized data will be shared with other researchers, upon request.

Supporting information: Study protocol, Analytic code

Time frame: The supporting information will be made available upon publication in the supporting documentation.

Access criteria: It will be made available in the supporting documentation.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 28, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05203575
Collaborators
Singapore Health Services
Responsible party
Lawrence Jin (Assistant Professor, National University of Singapore) — Principal investigator
First posted
Jan 24, 2022
Start date
Mar 28, 2022
Primary completion
Aug 31, 2023 (estimated)
Completion
Aug 31, 2023 (estimated)
Last update
Sep 28, 2022

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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