Testing the Effectiveness of Different Messaging Approaches to Increase Doctor Visits Amongst Individuals With Risk Factors for Diabetes

Sponsor
Wits Health Consortium (Pty) Ltd (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05755555
Collaborator
Discovery Vitality (Other)
5,000
1
3
8
628.9

Study Details

Study Description

Brief Summary

The purpose of the research is to test the effectiveness of different messaging approaches to nudge members of Vitality and Discovery Health, with risk factors for diabetes (based on data from the Vitality Health Check and Vitality Age assessment), to visit a doctor and test for diabetes. The messages are based on concepts from behavioural economics that aim to make information on screening more salient by using the concept of social proof (person like you) and an authoritative source (a diabetes specialist and the Vitality doctor).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Visit a doctor
N/A

Detailed Description

Members of Vitality who are also members of the Discovery Health medical plan and who have risk factors for diabetes but who have not previously been diagnosed with diabetes will be eligible for the study. Subjects will be identified based on the Vitality Age assessment and the Vitality Health Check done in the previous year. The risk factors identified by these assessments and which are important for eligibility are age ≥45years, overweight and obesity, family history of diabetes, hypertension or raised high blood pressure, low levels of physical activity, cardiovascular disease, and dyslipidemia. It is estimated that approximately 5000 Vitality members will be eligible for the study. Only the actuarial team assigned to the study will have access to the data. Participants will de-identified and randomly allocated to the control and four intervention arms. Messages will be sent via email to them which addresses their specific health risks and measures they can take to address those risk. The messages will be in an encrypted PDF sent by email. In compliance with the POPIA Act, as a first step, participants will be asked to provide consent, by confirming their ID number, to share their individual risks information with them. Messages sent via email will have the same basic structure. All three of the experimental arm messages will include the following:

  • The same subject line

  • A description of their risk factors for diabetes

  • A description of the benefits of visiting a doctor and getting screened for diabetes

Study Design

Study Type:
Interventional
Actual Enrollment :
5000 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Screening
Official Title:
Testing the Effectiveness of Different Messaging Approaches to Increase Doctor Visits to Confirm or Exclude a Diagnosis of Prediabetes or Diabetes Amongst Individuals With Risk Factors for Diabetes: A Randomised, Controlled Trial
Actual Study Start Date :
Aug 4, 2022
Anticipated Primary Completion Date :
Mar 3, 2023
Anticipated Study Completion Date :
Apr 3, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Diabetes specialist

Message with a note from a diabetes specialist

Behavioral: Visit a doctor
Test messages based on concepts from behavioural economics that aim to make information on screening more salient by using the concept of social proof (person like you) and an authoritative source (a diabetes specialist)

Experimental: Someone like you

Message with a note from "a person like you"

Behavioral: Visit a doctor
Test messages based on concepts from behavioural economics that aim to make information on screening more salient by using the concept of social proof (person like you) and an authoritative source (a diabetes specialist)

Experimental: Vitality doctor

Message with a note from the Vitality doctor

Behavioral: Visit a doctor
Test messages based on concepts from behavioural economics that aim to make information on screening more salient by using the concept of social proof (person like you) and an authoritative source (a diabetes specialist)

Outcome Measures

Primary Outcome Measures

  1. Fasting blood glucose (mmol/L) [8 weeks]

    Type 2 Diabetes

  2. Glucose tolerance test (mmol/L) [8 weeks]

    Type 2 Diabetes

  3. HbA1C(%) [8 weeks]

    Pre-Diabetes

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Members of Vitality who are also members of the Discovery Health medical plan and who have risk factors for diabetes but who have not previously been diagnosed with diabetes

  • Risk factors are age ≥45years, overweight and obesity, family history of diabetes, hypertension or raised high blood pressure, low levels of physical activity, cardiovascular disease, and dyslipidemia.

Exclusion Criteria:
  • < 18 years >= 65 years

  • Diagnosed with diabetes

Contacts and Locations

Locations

Site City State Country Postal Code
1 Discovery Vitality Johannesburg Gauteng South Africa 2007

Sponsors and Collaborators

  • Wits Health Consortium (Pty) Ltd
  • Discovery Vitality

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Wits Health Consortium (Pty) Ltd
ClinicalTrials.gov Identifier:
NCT05755555
Other Study ID Numbers:
  • M220715
First Posted:
Mar 6, 2023
Last Update Posted:
Mar 6, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 6, 2023