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Glaucoma Medication Adherence Study

Assessment of the role of regular text messages, audio-visual reminders using adherence monitors, and one on one counselling on the adherence to topical medications in patients with glaucoma - A non-randomized study - AGMAS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073433
Enrollment
100
Registered
2024-09-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: H401- Open-angle glaucoma

Interventions

Sponsors

W K Kellogg Eye Centre, Michigan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: as

Exclusion criteria

Exclusion criteria: 1. Newly diagnosed patients with glaucoma 2. Glaucoma patients with uncontrolled IOP 3. Glaucoma patients who are not on stable medications 4. Ocular hypertension (OHT) 5. Normal tension glaucoma 6. Secondary glaucomas like immediate post-surgical, steroid induced which might not need long term anti-glaucoma medications 7. History of intraocular surgery within the previous 3 months 8. People with cognitive decline – BCVA in the better eye less than 6/60, poor hearing requiring hearing aids 9. Illiterate patients 10. Pregnant / nursing mothers

Design outcomes

Primary

MeasureTime frame
1.To assess the change in mean adherence from baseline following regular text messages, audio-visual reminders using adherence monitors and counselling 2.To assess the proportion of participants with improved adherence from baseline following regular text messages, audio-visual reminders using adherence monitors and counselling Timepoint: 6 months

Secondary

MeasureTime frame
1. To assess the barriers for adherence based on a survey questionnaire 2. To assess the participant feedback regarding the three methods of intervention - regular text messages, audio-visual reminders using adherence monitors and counselling using a feedback form 3. To assess whether there is an incremental response in adherence when multiple methods are used sequentially 4. To assess the proportion of participants with =80% adherence Timepoint: 6 months

Countries

India

Contacts

Public ContactSwati Upadhyaya

Aravind Eye Hospital, Pondicherry

swati.dr@aravind.org8489810704

Outcome results

None listed

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