Data-Driven Lay First Responder Program in Cameroon
K-LFR Project
Implementation of a Data-Driven Pre-Hospital Lay First Responder Program in Cameroon
1 other identifier
interventional
1,812
1 country
1
Brief Summary
Cameroon experiences a high burden of injury-related morbidity and mortality and currently lacks a formal pre-hospital care system. Lay First Responder (LFR) programs have been implemented in several low-and middle-income countries to improve early injury care by training non-medical community members with high exposure to injury, such as commercial drivers, in basic first aid and safe transport of injured patients. The study aims to implement and evaluate a data-driven, context-adapted LFR program in Cameroon using an implementation science approach. Quantitative trauma registry data and qualitative stakeholder interviews will be used to adapt the LFR curriculum to local injury patterns and care gaps. LFR program implementation will be associated with increased chances of survival on presentation and improved trauma outcomes. The study is an interrupted time series evaluation of an LFR intervention where prehospital care rates and clinical patterns in the Cameroon Trauma Registry (CTR) patients at Limbe Regional hospital will be compared between historical pre-implementation controls and post-implementation of a data-driven lay first responder training program (the intervention).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 15, 2026
CompletedFirst Posted
Study publicly available on registry
May 12, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2028
Study Completion
Last participant's last visit for all outcomes
September 1, 2028
May 12, 2026
May 1, 2026
1.8 years
April 15, 2026
May 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Prehospital care rate
Proportion of hospitalized trauma patients who received prehospital care prior to arrival at participating hospitals, compared between pre- and post implementation LFR cohorts.
From enrollment through the 18-month post implementation period.
Secondary Outcomes (7)
Systolic blood pressure at presentation
From enrollment through the 18-month post implementation period.
Respiratory rate greater than 8 and less than 20 breaths per minute
From enrollment through the 18-month post-implementation period
Proportion of trauma patients with heart rate between 60 and 100 beats per minute
From enrollment through the 18-month post implementation period.
In-hospital mortality
From enrollment through the 18-month post-implementation period.
24-hour mortality
From enrollment through the 18-month post implementation period.
- +2 more secondary outcomes
Study Arms (2)
Pre-LFR implementation CTR cohort
NO INTERVENTIONHistoric data of trauma patients enrolled during an 18-month pre-implementation period in Limbe Regional Hospital before the LFR training program commences.
Post-LFR implementation CTR cohort
EXPERIMENTALTrauma patients enrolled in the 18- month post-implementation period in Limbe Regional Hospital after the 3-month LFR provider training program and transition period has ended.
Interventions
Training of LFR providers using a data driven, pretested curriculum adapted for the Cameroon context over a 3-month training and transition period.
Eligibility Criteria
You may qualify if:
- \- Trauma patients presenting to Limbe Regional Hospital and enrolled in the Cameroon Trauma Registry
You may not qualify if:
- \- Trauma patients not included in the Cameroon trauma registry at Limbe regional hospital.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sabrinah Christielead
- Fogarty International Center of the National Institute of Healthcollaborator
- University of Bueacollaborator
- University of California, Los Angelescollaborator
Study Sites (1)
Limbe Health District
Limbe, Southwest, Cameroon
MeSH Terms
Conditions
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SEQUENTIAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Assistant Professor of Surgery
Study Record Dates
First Submitted
April 15, 2026
First Posted
May 12, 2026
Study Start (Estimated)
September 1, 2026
Primary Completion (Estimated)
June 1, 2028
Study Completion (Estimated)
September 1, 2028
Last Updated
May 12, 2026
Record last verified: 2026-05