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NCT Number: NCT07416864

Enhancing Operational Efficiency in Eye Care Services

Pushpagiri Vitreo Retina Institute (PVRI) based in Secunderabad is a tertiary care eye hospital providing specialty eye care services since 2007. Over 15-20 preplanned surgical/clinical procedures are conducted for patients requiring care on a daily basis. They range from simple cataract surgeries or injections to detailed specialty surgeries including Vitreo-retina, glaucoma, pediatric eye care and muscular conditions of the eye. All procedures are elective procedures and are pre-planned. The current study aims to improve hospital efficiency and reduce the total appointment time for patients. The current study aims to reduce patient overall waiting time by 15-25% by introducing simple patient identification tools to help streamline all planned procedures.

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Key information

Age range

Up to 85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Pushpagiri Vitreo Retina Institute

Secunderabad, Telangana, India

Location status: Recruiting

Location contact

Dr. Bala Vidyadhar

CONTACT

[email protected]

+91 9482395316

About this study

PVRI operates close to 70-80 procedures daily. 15-20 pre-planned procedures are scheduled in the Secunderabad unit. All patients undergoing planned procedures on a daily basis spend close to 4-6 hours in the hospital. To understand the clinical workflow and time taken for the patient to undergo the procedure, a baseline assessment was conducted by the PVRI operational research team to measure the specific time taken for the patient to pass through the different sections of the hospital for undergoing any procedure.

Findings of the baseline assessment showed that waiting time was generally higher at >4 hours for all patients. The waiting time was specifically higher in the ward area before and after a procedure is done. Patients getting treated under the Cash or Third Party Administrator (TPA) category take twice as long as other categories finish billing procedures at the front office section. The individual waiting area in each section is listed on the table below.

S no Description Category Avg. Waiting time(Hr:Min)

  • Total Appointment Time Non-Cataract procedure 04:24 (TAT) Cataract procedure 04:09 Credit patients 04:23 Cash/TPA patient 04:05 EHS/ARG 03:53
  • Time spent at Front office/ Billing Cash-TPA 00:30 Credit/Cred + Enhanced 00:12 ARG/State Scheme 00:07 CGHS/SCCL/SCR/central 00:24
  • Ward Waiting Time (Pre-op) Non-Cataract 01:03 Cataract procedure 01:04
  • OR Table time Non-Cataract 00:49 Cataract procedure 00:39
  • Operation Theatre time (in-out of the dept) Overall average of all cases OT time 1:24
  • Average Recovery to discharge time Non-Cataract 01:33 Cataract procedure 01:51 Overall recovery average 01:44

Study Design

This study will adopt an operational research design using a mixed-methods approach, combining time-motion studies, process mapping, and intervention validation to optimize patient flow at Pushpagiri Vitreo Retina Institute (PVRI), Secunderabad unit. The design will follow three phases:

  • Baseline workflow analysis (already conducted and used as reference).
  • Development and implementation of interventions (checklists, billing streamlining, ward scheduling).
  • Post-intervention evaluation to measure efficiency gains against defined objectives.

Study Setting and Population The study will be conducted at PVRI Secunderabad unit, a super-specialty eye hospital performing 70-80 procedures daily, of which 15-20 are pre-planned surgical cases. All patients scheduled for planned surgical procedures (cataract and non-cataract) during the study period will be eligible. Subgroup analyses will be performed for payment categories (Cash/TPA, Credit, State/EHS schemes).

Sample Size Calculation for Reduction in Overall TAT

Since the study compares mean TAT before and after intervention, the sample size has been calculated using the formula for comparison of two means, n=(Z_(α/2)+Z_β )^2×2σ^2 ┤/d^2 n=(1.96+0.84)^2×2×120^2 ┤/38^2 = 156.4

Thus, the minimum required sample size is 157 patients per phase. A 15% adjustment has been applied to the minimum calculated sample size to account for operational data loss such as cancelled procedures and incomplete records. After inflation (157 × 1.15 = 181), the value was rounded to a practical range of 180-200 patients per phase. Therefore, the final planned sample size is approximately 400 patients in total, with 200 in the baseline phase and 200 in the post-intervention phase.

Interventions

  • Pre-operative segregation checklist:
  • Develop a standardized checklist validated by ophthalmologists and anesthetists & operational heads.
  • Pilot-test on a small group of patients before scaling.
  • Incorporate electronic/digital versions where feasible.
  • Reception and billing workflow redesign:
  • Introduce a fast-track billing process for Cash/TPA patients, drawing on evidence that optimized front-office processes reduce waiting time significantly (Kern et al., 2021).
  • Consider implementing token-based or electronic queue management.
  • Ward waiting time reduction:
  • Streamline surgical slot allocation using checklist-based segregation.
  • Allocate time slots and support nurses proactively based on procedure type.
  • Recovery and discharge process:
  • Develop discharge readiness criteria checklist to shorten recovery-to-discharge time.
  • Introduce counseling for patients/attendants while recovery monitoring is completed.

Data Collection Methods

  • Time-motion study: Direct observation with stopwatch/timestamp recording at each stage (front office, pre-op, ward, OT, recovery, billing).
  • Process mapping: Sequential workflow documentation through patient tracking sheets.
  • Operational logs: Data extraction from hospital information system (where available).

Data Analysis[BM1.1]

  • Descriptive statistics (mean, median, SD) to summarize time at each stage.
  • Paired t-tests or Wilcoxon signed-rank tests (depending on distribution) to compare pre- and post-intervention times.
  • Subgroup analyses by procedure type (cataract vs. non-cataract) and payment method.
  • Simulation modeling may be applied to validate checklist scheduling efficiency Ethical Considerations
  • Institutional Ethics Committee (IEC) approval will be obtained.
  • Informed consent will be taken from all patients included in the study.
  • Confidentiality of patient records will be maintained.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients undergoing pre-planned elective procedures in the unit listed on appointment basis.
  • Eligibility: Enrolment criteria: any patient undergoing any planned procedure is included on daily basis

Exclusion criteria

  • Patients undergoing emergency procedures.
  • Data for patients whose procedures were cancelled/postponed
  • Any other patients undergoing procedures under the free eye camps

Treatment and study plan

Health service Optimization

Other
  • Introduction of validated appointment checklist
  • Presence of single Point of Contact (POC) for patient transfer from Ward to OT to Ward
  • Standardize Discharge documentation protocol through EMR IP billing

Primary outcomes

  1. Patient appointment time

    Time frame: 6-8 months

    Reduction of overall Patient appointment time by 15-25%

Secondary outcomes

  1. Billing time

    Time frame: 6-8 months

    Reduction in billing time at reception by 20% for patients undergoing treatment through Cash/TPA payments

  2. Ward waiting time

    Time frame: 6-8 months

    Reduction in Ward waiting time of all patients undergoing cataract surgery by 20%

Sponsors and collaborators

Lead sponsor

Seva Canada Society

Other

Collaborators

  • Pragyaan Sustainable Health Outcomes Foundation
  • Pushpagiri Vitreo Retina Institute, Secunderabad

Registry information

Official study title

Enhancing Operational Efficiency in Eye Care Services: A Mixed-Methods Operational Research Study in a Tertiary Care Eye Hospital

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 18, 2026
Registry last updated
May 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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