Actively Recruiting
Enhancing Operational Efficiency in Eye Care Services: A Mixed-Methods Operational Research Study in a Tertiary Care Eye Hospital
Led by Seva Canada Society · Updated on 2026-05-05
400
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
Sponsors
S
Seva Canada Society
Lead Sponsor
P
Pushpagiri Vitreo Retina Institute, Secunderabad
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating ways to improve operational efficiency and reduce total appointment time for patients undergoing elective eye care procedures at Pushpagiri Vitreo Retina Institute (PVRI), a tertiary eye hospital in Secunderabad. This study focuses on reducing patient waiting time by 15-25% using simple patient identification tools to streamline planned surgical and clinical procedures. The study uses a mixed-methods operational research design including time-motion studies, process mapping, and intervention validation. The study involves implementing interventions such as a pre-operative segregation checklist, redesigning reception and billing workflows to introduce fast-track billing for some payment categories, streamlining surgical slot allocation in wards, and improving recovery and discharge processes through checklist-based criteria and patient counseling. These interventions are applied after a baseline workflow analysis has been conducted to measure current patient flow and waiting times. Participants are patients scheduled for pre-planned elective eye procedures during the study period. Researchers will observe and record time spent at different hospital sections such as front office, ward, operation theatre, and recovery. Data analysis will compare pre- and post-intervention times to measure efficiency improvements. The primary outcome is patient appointment time over 6-8 months, with secondary outcomes including billing and ward waiting times. The study includes informed consent, ethical approval, and maintains patient confidentiality.
CONDITIONS
Brief Title
Enhancing Operational Efficiency in Eye Care Services
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing pre-planned elective procedures at the hospital
- Patients scheduled on an appointment basis for planned procedures
- Patients of all genders up to 85 years old
You will not qualify if you...
- Patients undergoing emergency eye procedures
- Patients whose procedures were cancelled or postponed
- Patients receiving treatment through free eye camps
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 to 8 months
Participants undergo planned eye procedures with operational improvements including a validated appointment checklist, a single point of contact for patient transfer, and standardized discharge documentation to optimize patient flow and reduce waiting times.
Multiple visits corresponding to scheduled procedures and associated care
Trial Site Locations
Total: 1 location
1
Pushpagiri Vitreo Retina Institute
Secunderabad, Telangana, India
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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