Quality ImprovementNCT07416864
Enhancing Operational Efficiency in Eye Care Services
A study testing Health service Optimization in people with Quality Improvement and Appointments and Schedules, run by Seva Canada Society at 1 site in India.
Trial summary
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. Read more about this study
- Who is it for?
- Ages Up to 85 years
- Conditions the study is for
- Quality Improvement, Appointments and Schedules, Operations Research Workflow
- What is being tested?
- Health service Optimization
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 400 participants
- Where
- 1 siteIndia
- Study dates
- 1 Mar 2026to Dec 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Up to 85 years
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- 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
Who cannot join
- Patients undergoing emergency procedures.
- Data for patients whose procedures were cancelled/postponed
- Any other patients undergoing procedures under the free eye camps
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
India1 site, 1 recruiting
- Recruiting
Pushpagiri Vitreo Retina Institute
Secunderabad, Telangana
Dr. Bala Vidyadhar, +91 9482395316, msbv.drrop@pvri.org
About this study
Official title: Enhancing Operational Efficiency in Eye Care Services: A Mixed-Methods Operational Research Study in a Tertiary Care Eye Hospital
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.
Read the detailed description
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.
- Being tested
- Health service Optimization
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Health service OptimizationOther
- 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
| Study group | Role | What they receive |
|---|---|---|
| Intervention arm | Experimental | Not described Receives: Other: Health service Optimization |
What is being measured
The primary outcome is the main question the study is designed to answer.
Patient appointment time
Reduction of overall Patient appointment time by 15-25%
Measured: 6-8 months
Secondary outcomes (2)
Billing time
Reduction in billing time at reception by 20% for patients undergoing treatment through Cash/TPA payments
Measured: 6-8 months
Ward waiting time
Reduction in Ward waiting time of all patients undergoing cataract surgery by 20%
Measured: 6-8 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Feb 2026
- Study start1 Mar 2026
- Primary completionSep 2026 (estimated)
- Study completionDec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Quality ImprovementStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 400 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Seva Canada Society
- Sponsor type
- University, hospital or other
- Collaborators
- Pushpagiri Vitreo Retina Institute, Secunderabad, Pragyaan Sustainable Health Outcomes Foundation
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07416864
- Sponsor's protocol ID
- PVRI-ORCB-0001
- Status last verified
- Apr 2026
- First submitted
- 10 Feb 2026
- Last updated
- 5 May 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 5 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Enhancing Operational Efficiency in Eye Care Services: A Mixed-Methods Operational Research Study in a Tertiary Care Eye Hospital
- ClinicalTrials.gov ID
- NCT07416864
- Acronym / sponsor ID
- PVRI-ORCB-0001
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 400 participants (estimated)
- Lead sponsor
- Seva Canada SocietyUniversity, hospital or other
- Collaborators
- Pushpagiri Vitreo Retina Institute, Secunderabad, Pragyaan Sustainable Health Outcomes Foundation
- Study start
- 1 Mar 2026 (actual)
- Primary completion
- Sep 2026 (estimated)
- Study completion
- Dec 2026 (estimated)
- First posted
- 18 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
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.
Study design
- Primary purpose
- Health services research
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Intervention arm | Experimental | Other: Health service Optimization |
Who may qualify
- Ages
- Up to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (2 listed)
- 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
Key exclusion criteria (3 listed)
- Patients undergoing emergency procedures.
- Data for patients whose procedures were cancelled/postponed
- Any other patients undergoing procedures under the free eye camps
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Health service Optimization* 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 | Other | Intervention arm |
Primary outcome
Patient appointment time
Time frame: 6-8 months
Reduction of overall Patient appointment time by 15-25%
2 secondary outcomes
Billing time
Time frame: 6-8 months
Ward waiting time
Time frame: 6-8 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 May 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Health service Optimization in people with Quality Improvement and Appointments and Schedules, run by Seva Canada Society at 1 site in India.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 5 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in India. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Patient appointment time (time frame: 6-8 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 May 2026.