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Structured Trauma Quality Improvement Meetings at Four Trauma Centres in India

Structured Trauma Quality Improvement Meetings at Four Trauma Centres in India: Protocol for a Prospective Observational Study to Assess Effectiveness

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03005509
Acronym
TQI
Enrollment
1500
Registered
2016-12-29
Start date
2017-01-31
Completion date
2018-03-31
Last updated
2019-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Injuries Major, Major Trauma

Keywords

Quality improvement, Injury, Injuries

Brief summary

A prospective before-and-after study to evaluate the effect of implementing a Trauma Quality Improvement protocol on the process of Trauma Quality Improvement meetings and major trauma patient outcomes at four trauma centres in India.

Detailed description

This project will be conducted as a prospective before-and-after study at four major trauma centres in India, with the intervention occurring between pre- and post-intervention phases. Included in the study will be all patients presenting to any of the four trauma hospitals with a potentially life-threatening or limb-threatening injury. The intervention will be the introduction of a structured Trauma Quality Improvement Meeting (TQIM), using a checklist and training program. The primary outcome will be compliance with the TQIM checklist, measured as the proportion of discussed cases (trauma deaths) for which problems with care, preventability and corrective actions were discussed and / or agreed. The secondary outcomes will include in-hospital risk-adjusted mortality, hospital length of stay and time to emergency surgery. Data collection will occur at all meetings at the four trauma hospitals at which trauma deaths are discussed. Data will also be collected in a dedicated trauma registry.

Interventions

OTHERTQIM checklist

The intervention phase will include an intense training period covering: 1. Conduct of Trauma Quality Improvement Meeting (TQIM) (and Trauma Quality Improvement program in general). The training will be delivered using the World Health Organization (WHO) Trauma Quality Improvement Programmes short course and online resources. 2. Implementation of Trauma Quality Improvement Meeting (TQIM) Checklist.

Sponsors

National Trauma Research Institute
CollaboratorOTHER
The Alfred
CollaboratorOTHER
Monash University
CollaboratorOTHER
All India Institute of Medical Sciences
CollaboratorOTHER
The George Institute for Global Health, Australia
CollaboratorOTHER
Sheth Vadilal Sarabhai General Hospital
CollaboratorOTHER
Guru Teg Bahadur Hospital
CollaboratorOTHER
Lokmanya Tilak Municipal Medical College and Hospital
CollaboratorOTHER
Centralised Accident and Trauma Services, Delhi, India
CollaboratorOTHER_GOV
GVK EMRI: Emergency Management and Research Institute
CollaboratorOTHER
Maharashtra Emergency Medical Services, India
CollaboratorOTHER
Nathiba Hargovandas Lakhmichand Municipal Medical College, India
CollaboratorUNKNOWN
University College of Medical Sciences, India
CollaboratorINDIV
Dr Gerard O'Reilly
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients presenting to any of the four study sites with a potentially life-threatening or limb-threatening injury. Specifically, all presenting injured patients triaged as Red or Yellow according to the Australia-India Trauma Systems Collaboration (AITSC) Trauma Triage Protocol, will meet the screening criteria for data collection. Retrospective inclusion in the registry will be continued for all screened patients presenting to any of the included hospitals with injury (including near-drowning) as the primary diagnosis and with at least one of the following criteria: * Admission to hospital * Death after triage but before admission

Exclusion criteria

* The

Design outcomes

Primary

MeasureTime frameDescription
TQIM Checklist compliance - preventabilityUp to 14 monthsTQIM Checklist compliance - % of cases for which it is agreed that care can be improved

Secondary

MeasureTime frameDescription
TQIM Checklist compliance - corrective actionUp to 14 monthsTQIM Checklist compliance - % of cases (where it is agreed that care can be improved) for which at least one corrective action is agreed
In hospital risk-adjusted mortalityUp to 14 monthsIn-hospital risk-adjusted mortality: The proportion of deaths amongst those with Injury Severity Score (ISS) \>12 and \<50.
Hospital length of stayUp to 14 monthsHospital length of stay
Time to emergency surgeryUp to 14 monthsTime from hospital arrival to operating theatre for patients undergoing emergency surgery

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026