Actively Recruiting

Phase Not Applicable
Age: 0 - 85Years
All Genders
ID07416864

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

Age: 0 - 85Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Intervention

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

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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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