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Feasibility of an interactive, SMS-based diabetes distress support program for Type 1 Diabetes patients

Feasibility of an interactive, SMS-based diabetes distress support program for Type 1 Diabetes patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623000978662
Acronym
T1DDS
Enrollment
90
Registered
2023-09-08
Start date
2025-03-03
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

None listed

Brief summary

A six-month study comparing usual clinical care (face to face appointments every 3 months) to usual care plus an SMS-based diabetes support program. HYPOTHESIS: We hypothesize that an SMS-based support program (SMS4T1D) will be feasible in the RPAH Diabetes Centre type 1 diabetes population and that this SMS-based program will facilitate a greater decrease in diabetes distress than standard clinical care over a six-month period. AIM: The primary aim of this study is to assess the feasibility of an SMS-based, diabetes distress support program in the RPAH Diabetes Centre type 1 diabetes population. The secondary aim is to estimate the likely magnitude of change in diabetes distress associated with the SMS4T1D program. This data could then be used to inform power calculations for future studies involving the SMS-based support program.

Interventions

A pilot, randomised controlled trial designed to test the feasibility of an interactive, SMS-based diabetes distress support program over a 6-month period against standard of care at the Royal Prince Alfred Hospital) RPAH Diabetes Centre. The pilot RCT will assess current clinic standard of care (Strategy A) against clinic standard of care plus SMS support (Strategy B). All participants will complete the T1-DDS score, PAID-5 score, DES-SF score, DSAS-1 score on two occasions, at baseline and at

A pilot, randomised controlled trial designed to test the feasibility of an interactive, SMS-based diabetes distress support program over a 6-month period against standard of care at the Royal Prince Alfred Hospital) RPAH Diabetes Centre. The pilot RCT will assess current clinic standard of care (Strategy A) against clinic standard of care plus SMS support (Strategy B). All participants will complete the T1-DDS score, PAID-5 score, DES-SF score, DSAS-1 score on two occasions, at baseline and at six-months. All participants will complete the T1-DDS score, PAID-5 score, DES-SF score, DSAS-1 score on two occasions, at baseline and at six-months. Strategy A – Current standard of care (Quarterly - once every 3 months) • Quarterly in-person clinic appointments at the Diabetes Centre or via telehealth (with Endocrinologist and Diabetes Educator) for review of glycaemia, routine pathology test results, complication screening and treatment adjustment • Dietary review/education with the Diabetes Centre Dietitian (as required) • Provision of a personal blood glucose monitor (or an alternative monitoring modality – Continuous Glucose Monitoring (CGM) or flash glucose monitoring) for self-monitoring of glycaemia at home Strategy B – Standard of care PLUS SMS support (SMS4T1D) • Current standard of care PLUS • A semi-personalised (male/female, name), twice weekly SMS relating to diabetes management (including general diabetes information [healthy eating, hypo support] and reminders about diabetes-specific self-care measures) • An option to engage with staff of the RPAH Diabetes Centre between routine clinic visits by sending diabetes-related questions via an SMS portal and receive a reply within one business day.

Sponsors

Sydney Local Health District
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

1. Patients with type 1 diabetes. 2. Over 18 years of age. 3. Willingness to provide informed consent and willingness to participate and comply with the study requirements. 4. Access to a mobile telephone to participate in the SMS-based program.

Exclusion criteria

1. Insufficient proficiency in English to participate in the interactive, SMS-based support program. 2. Participants with a history of a psychological illness or other conditions which may interfere with their ability to understand the study requirements.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026