About this trial
Cataract remains the leading cause of avoidable blindness in India despite substantial expansion of surgical services over the past two decades. While surgical coverage has improved, optimal visual outcomes depend on effective post-operative follow-up, which remains inconsistent across decentralized Vision Center-based systems, particularly in rural and semi-urban settings. Routine program data show wide variation in post-operative cataract follow-up compliance among Vision Centers operating within similar organizational and geographic contexts, suggesting the influence of facility-level determinants.
This phased mixed-methods implementation study aims to identify facility-level factors influencing post-operative cataract follow-up compliance and to develop an evidence-based framework to strengthen follow-up systems. Phase 1 will involve retrospective analysis of three years of integrated Health Management Information System- Vision Centre Management Information System (HMIS-VCMIS) data from approximately 120 Vision Centers to establish empirical benchmarks and classify centers as high- or low-performing. Structured facility assessments and qualitative interviews with Vision Center staff, program managers, and post-operative patients will be conducted to identify operational practices, workflows, and contextual factors associated with follow-up performance.
Phase 2 will focus on co-design, pilot testing, and early implementation of a Follow-Up Strengthening Intervention Framework in selected low-performing Vision Centers. The intervention will include standardized counselling workflows, follow-up tracking and reminder systems, role clarification, supervisory feedback mechanisms, and peer-learning support from high-performing centers. Changes in follow-up compliance will be monitored using routine data over a 12-month implementation period, alongside process evaluation to assess feasibility, fidelity, and acceptability.
Findings from this study will generate practical evidence to strengthen post-operative cataract follow-up systems and inform scalable quality improvement strategies within decentralized Vision Center networks.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥40 years
All cataract surgery types (e.g., SICS, phacoemulsification)
Advised Vision Center follow-up at discharge
Complete HMIS-VCMIS linkage
Disqualifiers
Age <40 years
Non-cataract surgeries
No advised Vision Center follow-up
Trial design
Single group
Treatments tested in this trial
Follow-Up Strengthening Intervention Framework
Other interventionThe intervention will include standardized counselling workflows, follow-up tracking and reminder systems, role clarification, supervisory feedback mechanisms, and peer-learning support from high-performing centers.
Treatment groups
Trial outcomes
Primary outcomes
Post-operative follow-up compliance
The primary outcome will be defined as facility-level postoperative follow-up compliance, calculated as the proportion of cataract patients who complete at least one follow-up visit at a Vision Center within 1 month (±15 days) of surgery. The denominator will include patients advised to follow up with the Vision Center at discharge, and the numerator will include those who completed the follow-up within this time window. The outcome will be based on HMIS-VCMIS linked patient records and analyzed at the Vision Center level over a 12-month observation period.
Locations
Sponsors and contacts
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Seva Canada Society
Lead sponsor
Sadgura Netra Chikitsalaya
Collaborator
Pragyaan Sustainable Health Outcomes Foundation
Collaborator
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