Improvement of Ambulance Response Times in Karachi, Pakistan
NCT ID: NCT02743169
Last Updated: 2020-08-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
OBSERVATIONAL
2017-04-01
2020-06-29
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluating the Integration of the Recommended Summary Plan for Emergency Care Treatment (ReSPECT) Into Primary Care
NCT05046197
Analyzing Patient Flows at the Emergency Department by Data Analytics, Simulation, and Optimization
NCT05025683
Trends of the Pre-hospital Emergency Care Spectrum in Beijing From 2005 to 2014: A Retrospective Analysis
NCT02645877
Evaluation of the Diagnostic Value of the TPD System in Determining ADHF Causing Acute Dyspnea
NCT03998410
Development of a Multipurpose Dashboard to Monitor the Situation of Emergency Departments
NCT06372379
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Low- and middle-income countries (LMICs) shoulder a disproportionate burden from acute illnesses, yet it has also been demonstrated that reduced transport times to a hospital decrease the odds of mortality in trauma patients in LMICs. A lack of equipment, poorly developed infrastructure, and long distances have been reported as key barriers in the provision of emergency care. Pakistan is one such LMIC that is burdened by many of these challenges in prehospital care. Emergency medical systems (EMS) have only recently been established in Pakistan, and prior to the last several years, patients were routinely transported to healthcare facilities by relatives, bystanders, or by basic patient transport. Where formal patient transport is available, transport times are often prolonged by distance, traffic congestion, and a lack of public cooperation.
Geographic information systems (GIS) are an analytic method that may serve as a key tool in decreasing the time of transporting acutely ill patients to life-saving medical care. GIS, which links geographic information to public health data, has been used in simulations to decrease ambulance response times and been shown to decrease response times in industrialized countries. However, this has not been replicated in other highly developed countries and has never been demonstrated in an LMIC.
The investigators hypothesize that that spatial analysis of the location data of ambulance calls can improve prehospital care provided by Aman Health Care Services in Karachi, Pakistan by decreasing ambulance response times for high acuity patients.
Aim 1: Develop a conceptual framework for prehospital care in LMICs. As no such framework currently exists in the literature, the investigators will develop a conceptual framework to anchor this project in Aims 2 and 3. The framework will be developed after a consideration of other related health systems frameworks in the literature. The investigators will also consult with experts in the field and with the partners in Karachi to comment on how the framework can be improved.
Aim 2: Analyze the location of calls to identify geographic areas with longer calls and higher severity of illness. Using GIS and spatial analysis, the investigators will analyze Aman Ambulance's existing data on ambulance calls to find areas of Karachi that routinely have long response times.
Aim 3: Position ambulances where there are clusters of delayed ambulance calls for high acuity patients to improve response times. Over a six-month period, ambulances will be repositioned in and around clusters of delays to improve response times. This period will be compared with the same calendar period in the previous year using a logistic regression analysis to determine if there is a decrease in delayed ambulance responses. Spatial analyses will also be performed on data from the intervention period to assess for the presence of clusters of delays.
This study has the potential to use a sustainable method of analyzing routinely collected data on ambulance calls to shorten the time that patients with acute illnesses receive appropriate medical care in Pakistan, a setting in which there are substantial infrastructure and human resource challenges.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Standard Practice
This group will consist of ambulance calls under the standard practice of Aman Foundation for ambulance placement.
No interventions assigned to this group
Post-Intervention
This group will consist of ambulance calls after the spatially-optimized placement of ambulances.
Spatially-Optimized
Spatial analysis of retrospective data will be used to optimize the placement of ambulances to decrease response time from the time the call is received until the time the ambulance arrives at the patient's location.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Spatially-Optimized
Spatial analysis of retrospective data will be used to optimize the placement of ambulances to decrease response time from the time the call is received until the time the ambulance arrives at the patient's location.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Johns Hopkins University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Kiemanh Pham, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
Johns Hopkins School of Medicine
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Aman Foundation
Karachi, , Pakistan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
IRB00085859
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.