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Not yet recruitingNCT07581327K-LFR ProjectUpdated May 12, 2026

Data-Driven Lay First Responder Program in Cameroon

An interventional study of Lay First Responder (LFR) training in Trauma and Injury, sponsored by Sabrinah Christie. Not yet recruiting at 1 site in Cameroon. Per ClinicalTrials.gov, last updated 2026-05-12.

Sponsored by Sabrinah Christie · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
1,812
Allocation
Non-randomized
Sex
All
01

Study 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).

Read the detailed description

Injury accounts for a substantial proportion of preventable mortality in Cameroon, where no organized prehospital emergency medical system currently exists. Evidence suggests that effective prehospital care could prevent up to 45% of injury-related deaths. Lay First Responder (LFR) programs represent a pragmatic strategy for improving early trauma care in resource-limited settings by training lay persons who are frequently present at injury scenes.

Despite promising early results in other settings, rigorous evaluation of LFR programs has been limited, particularly regarding their impact on patient-level outcomes. This study aim to test the contextual feasibility of the lay first responder program in Cameroon, after it has been successful in other Sub-Saharan nations.

This study seeks to address these gaps by implementing a data-driven LFR program informed by trauma registry analysis and stakeholder engagement, and by evaluating feasibility, acceptability, and effectiveness within Cameroonian context.

The Cameroon Trauma Registry (CTR) gathers prospective data on patient demographics, injury characteristics, receipt of prehospital care, clinical findings and management, disposition and outcomes on patients admitted for injuries at ten trauma hospitals in Cameroon. Each hospital has a full-time research assistant overseen by an MPH-level field supervisor. Patients are followed from presentation through hospital discharge. This study will be implemented in Limbe municipality, Cameroon and will utilize data from the Limbe Regional Hospital site of the CTR.

The LFR intervention: An LFR curriculum adapted for the Cameroon context using a two-stage, mixed-methods approach (quantitative analysis of prospective CTR data and qualitative semi-structured interviews of target stakeholders) will be used to train LFR providers (commercial drivers and community members) over a 3-month training and transition period.

The primary metric of program feasibility will be percent change in the proportion of trauma patients receiving prehospital care in the post-intervention cohort compared to pre-intervention historical controls. The secondary outcomes for program effectiveness will be injury severity-stratified percentage change in the proportion of CTR patients presenting with normal vital signs (systolic blood pressure, heart rate, respiratory rate) in the post-intervention cohort compared to the pre-intervention cohort.

02

Conditions studied

  • Trauma
  • Injury

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Keywords

  • Lay First Resposnder
  • Trauma
  • Pre-Hospital care
  • Road Traffic Injury
  • By-stander response
  • Trauma systems
  • Emergency Care
03

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

- Trauma patients presenting to Limbe Regional Hospital and enrolled in the Cameroon Trauma Registry

Exclusion criteria

Exclusion Criteria

- Trauma patients not included in the Cameroon trauma registry at Limbe regional hospital.

04

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
1,812 participants (estimated)

Study arms

  • No intervention
    Pre-LFR implementation CTR cohort

    Historic data of trauma patients enrolled during an 18-month pre-implementation period in Limbe Regional Hospital before the LFR training program commences.

  • Experimental
    Post-LFR implementation CTR cohort

    Trauma 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.

    Behavioral: Lay First Responder (LFR) training

Interventions

  • BehavioralLay First Responder (LFR) training

    Training of LFR providers using a data driven, pretested curriculum adapted for the Cameroon context over a 3-month training and transition period.

05

What researchers measure

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.

    Time frame: From enrollment through the 18-month post implementation period.

Secondary outcomes

  1. Systolic blood pressure at presentation

    Median systolic blood pressure (mmHg) measured at hospital presentation among injured patients, compared between pre- and post implementation LFR cohorts

    Time frame: From enrollment through the 18-month post implementation period.

  2. Respiratory rate greater than 8 and less than 20 breaths per minute

    Percentage change in the proportion of CTR patients presenting with respiratory rate greater than 8 and less than 20 breaths per minute compared between pre- and post implementation LFR cohorts.

    Time frame: From enrollment through the 18-month post-implementation period

  3. Proportion of trauma patients with heart rate between 60 and 100 beats per minute

    Percent change in the proportion of trauma patients with heart rate between 60 and 100 beats per minute compared between pre- and post implementation LFR cohorts.

    Time frame: From enrollment through the 18-month post implementation period.

  4. In-hospital mortality

    All-cause in-hospital mortality among injured patients, compared between pre- and post implementation LFR cohorts.

    Time frame: From enrollment through the 18-month post-implementation period.

  5. 24-hour mortality

    All-cause mortality within 24 hours of hospital presentation among injured patients, compared between pre- and post implementation LFR cohorts.

    Time frame: From enrollment through the 18-month post implementation period.

  6. Blood transfusion

    Proportion of injured patients receiving blood transfusion during hospitalization, compared between pre- and post implementation LFR cohorts.

    Time frame: From enrollment through 18-month post implementation period.

  7. Operative intervention

    Proportion of injured patients requiring surgical intervention during hospitalization, compared between pre- and post implementation LFR cohorts.

    Time frame: From enrollment through 18-month post implementation period.

06

Study locations

1 site
  • Limbe Health District
    Limbe, Southwest, Cameroon
07

References and documents

Study documents

  • Protocol and statistical analysis plan · Oct 23, 2024

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Undecided

08

Registry details

Key details

Study ID
NCT07581327
Lead sponsor
Sabrinah Christie
Collaborators
Fogarty International Center of the National Institute of Health, University of Buea, University of California, Los Angeles
Responsible party
Sabrinah Christie (Assistant Professor of Surgery, University of California, Los Angeles) — Sponsor-investigator
First posted
May 12, 2026
Start date
Sep 2026 (estimated)
Primary completion
Jun 2028 (estimated)
Completion
Sep 2028 (estimated)
Last update
May 12, 2026

Study contacts

S.Ariane Christie, BA, MD
Contact
s.ariane.christie@gmail.com
808-430-9678
Isaac Obeng-Gyasi, MBChB, MPH
Contact
iobeng@mednet.ucla.edu
202-500-4230

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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