Skip to content

A Smartphone Application to Improve Medication Adherence Among People With Type 2 Diabetes Mellitus in Singapore

A Smartphone Application to Improve Medication Adherence Among People With Type 2 Diabetes Mellitus in Singapore: A Randomized Controlled Trial

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02105597
Acronym
iADHERE
Enrollment
0
Registered
2014-04-07
Start date
2014-08-31
Completion date
Unknown
Last updated
2017-02-10

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

Conditions

Diabetes Mellitus

Keywords

Diabetes mellitus, Medication adherence, Compliance, Mobile health

Brief summary

Background: Diabetes mellitus (DM) is a major cause of morbidity and mortality worldwide. Long-term glycemic control is important to prevent or delay the onset of DM related complications. Patients often fail to achieve optimal glycemic control from pharmacotherapy due to non-adherence. With the high prevalence of smartphone usage locally and among the developed countries, there has been a growing interest to deliver interventions through mobile applications. In this study, a mobile application targeted at improving medication adherence among people with Type 2 DM will be developed and evaluated. Aims: This study aims to (i) design a smartphone application to improve medication adherence and (ii) evaluate its impact on clinical outcomes, health-related quality of life (HRQoL) and health status among patients with Type 2 DM. Hypothesis: The use of a smartphone application can improve medication adherence among patients with Type 2 DM, as well as clinical outcomes, HRQoL and health status. Methods: This is a randomized, open-label controlled trial involving patients with Type 2 DM managed at Singapore General Hospital. Patients seen at the institution's Diabetes Centre and those referred to the pharmacist-led Medication Therapy Management service are eligible to participate. Patients in the intervention group will have the mobile application downloaded onto their smartphones, while those in the control group will receive the usual standard of care. The primary outcome will be change in self-reported medication adherence, determined using the 8-item Morisky Medication Adherence Scale. Secondary outcomes include change in HbA1c, blood glucose, frequency of dose titrations, addition or removal of oral hypoglycemic agents, HRQoL (measured using the Audit of Diabetes Dependent Quality of Life) and health status (measured using the EuroQol-5D-5L and EuroQol Visual Analogue Scale). All outcomes will be measured at baseline and at the end of the 6-month study period (± 4 weeks). Significance: The development and evaluation of a mobile application to improve adherence among patients with Type 2 DM in Singapore is the first of its kind, and the findings of this study will provide the much-needed evidence to demonstrate the effectiveness of this intervention.

Interventions

OTHERMobile application

The intervention in this study is a mobile application which will be downloaded into the participant's smartphone.

Sponsors

National University of Singapore
CollaboratorOTHER
Singapore General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* Existing Type 2 DM managed at SGH Diabetes Centre and those referred to the pharmacist-led MTM service * Age≥ 40 years * HbA1c≥ 8.0 * Suspected non-adherence (e.g. admitted to have missed doses, HbA1c not at target despite frequent dose titrations, recent DM related hospitalization/ emergency visit) * Owns a iOS smartphone with Wi-Fi or data plan

Exclusion criteria

* Unable to manage own medications (e.g. taken care of by caregiver, nursing home patients, cognitive impairment) * Unable to read and comprehend English * Physical impairment that precludes the use of smart phone functions (e.g. deformed finger joints, amputation)

Design outcomes

Primary

MeasureTime frameDescription
Change in self-reported medication adherenceBaseline (at recruitment) and 6 months (+/- 4 weeks)Self-reported medication adherence will be assessed using the 8-item Morisky Medication Adherence Scale.

Secondary

MeasureTime frameDescription
Change in blood glucoseBaseline (at recruitment) and 6 months (+/- 4 weeks)Part of routine monitoring during doctor's appointment
Frequency of dose titrations of oral hypoglycemic agents and insulin6 months (+/- 4 weeks) after recruitment
Change in HbA1cBaseline (at recruitment) and 6 months (+/- 4 weeks)Part of routine monitoring during doctor's appointment
Change in health-related quality of lifeBaseline (at recruitment) and 6 months (+/- 4 weeks)Measured using Audit of Diabetes Dependent Quality of Life - 19 (ADDQoL-19) questionnaire
Change in health statusBaseline (at recruitment) and 6 months (+/- 4 weeks)Measured using EuroQol-5D-5L and EuroQol Visual Analogue Scale.
Addition or removal of oral hypoglycemic agents and insulin6 months (+/- 4 weeks) after recruitment

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026