Follow-up Compliance for Corneal Ulcer Patients With SMS Reminder

ConditionCorneal Ulcer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorSeva Canada Society

About this trial

Corneal ulcer is defined as the loss of corneal epithelium with underlying stromal infiltration and suppuration, accompanied by signs of inflammation, with or without hypopyon1. The condition may be caused by bacterial, fungal, viral or parasitic pathogens and carries a significant risk of corneal perforation and subsequent visual impairment2. These risks highlight the importance of timely treatment plans and consistent referral networks3.

A lot of patients choose to self-medicate and postpone seeking professional assistance due either their lack of awareness or forgetfulness, which results in inadequate follow-up compliance4,5. Scheduling appointments regularly is still a significant barrier to successful treatment and visual recovery.

SMS reminders have shown encouraging real-world success in improving follow-up attendance with in ophthalmology. Mobile health tools, such as the peek Community Eye Health system, have proven increased follow-up rates and improved access to eye care services in low-resource setting through automated appointment reminders and patient monitoring6.

The aim of this operational research study to evaluated the feasibility, scalability, and effectiveness of SMS reminders in improving follow-up compliance among patients with corneal ulcer at the Lumbini Eye Institute and Research Center (LEIRC), Western Nepal. The findings are expected to inform the integration of cost-effective digital health strategies to strengthen patient adherence, optimize clinical outcomes, and support eye health programs in resource limited environments.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Newly diagnosed patients (18 to 70 years) of corneal ulcer in one or both eye, who are medically managed, visiting the OPD at LEIRC and have access to a mobile phone.

Disqualifiers

Less than 18 years or more than 70 years Patients who do not have a access to a mobile phone.

Trial design

Design model

Parallel

Treatments tested in this trial

  • SMS reminder

    Other intervention

    Patients presenting on Monday, Wednesday, and Friday for the first time for treatment will be recruited in the intervention group. For those who are recruited after receiving informed consent, SMS reminders before scheduled follow-up will be sent from the hospital regarding the next scheduled visit. In addition, routine counselling will be done during the first visit regarding the follow-up schedule.

Treatment groups

310 Participants
are divided into 2 treatment groups
Group A: SMS reminder groupExperimental treatment 1 intervention
Group B: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Follow-up compliance

Proportion of patients who comply with scheduled follow-up visits during the study period

Time frame
6 months

Secondary outcomes

1

Cost effectiveness

Direct and indirect cost of the SMS and routine counselling services.

Time frame
6 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Seva Canada Society

Lead sponsor

Lumbini Eye Institute and Research Centre

Collaborator

Pragyaan Sustainable Health Outcomes Foundation

Collaborator