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Supporting Laypeople Addressing Prehospital Hemorrhage Study

NCT05812352 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 205

Last updated 2023-12-13

No results posted yet for this study

Summary

It is unknown if bystanders equipped with point-of-care (POC) instruction are as effective as bystanders with in-person training for bleeding control. Therefore, POC instructional interventions were developed during this study in response to the scalability challenges associated with in-person training to measure the comparative effectiveness and skill retention of POC instructions vs in-person training using a randomized clinical trial design.

Conditions

Interventions

BEHAVIORAL

Audio kit

MP3 audio files for each of 6 steps and instructional flashcard with pictures corresponding to each of the 6 steps of tourniquet application

BEHAVIORAL

Instructional flashcard

Single page (instructional flashcard) with pictures corresponding to each of the 6 steps of tourniquet application

BEHAVIORAL

In-person training

Stop the Bleed bleeding control (B-Con) course is used for instruction for tourniquet application attempt

Sponsors & Collaborators

  • Washington University School of Medicine

    collaborator OTHER

  • LFR International

    collaborator UNKNOWN

  • University of Michigan

    lead OTHER

Principal Investigators

  • Zachary Eisner, BS · University of Michigan

  • Patricia Widder, MS · Washington University in St. Louis - McKelvey School of Engineering

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-01-24
Primary Completion
2023-12-01
Completion
2023-12-01

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05812352 on ClinicalTrials.gov