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Mobile application Vs conventional diary method on medication adherence among diabetic subjects

Impact of mobile application and conventional diary method on the adherence to the medications among subjects attending Diabetes clinic in a tertiary care center of eastern India: A randomized pilot study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099891
Enrollment
120
Registered
2025-12-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: E119- Type 2 diabetes mellitus without complications

Interventions

Intervention1: Medisafe Mobile Application: A smartphone-based platform designed to support patients in managing their medication schedules through features like timely reminders, dose tracking, adher

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged 18 70 years with type 2 diabetes mellitus On stable oral hypoglycemic agents insulin for at least 3 months Owns a smartphone (for Medisafe arm) Provides informed consent.

Exclusion criteria

Exclusion criteria: Cognitive impairment or psychiatric illness interfering with adherence. Severe diabetic complications (e.g., end-stage renal disease, advanced retinopathy). Participation in another adherence-related trial.

Design outcomes

Primary

MeasureTime frame
Medication adherence measured using: MARS Medication Adherence Scale (MARS 5) at baseline and 24 week Pill count method at each follow-up visit. Timepoint: Baseline and 24 Weeks

Secondary

MeasureTime frame
Change in HbA1c at baseline and at the end of 12 weeks and 24 weeks Fasting and postprandial blood glucose values. Renal parameters like blood urea, serum creatinine and spot urine albumin creatinine ratio were reassessed after 12 and 24 weeks and compared with the baseline values Patient satisfaction and ease-of-use (Likert scale questionnaire). Timepoint: 12 weeks and 24 Weeks

Countries

India

Contacts

Public ContactShatavisa Mukherjee

School of Tropical Medicine, Kolkata

shatavisa100@gmail.com9830529192

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026