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Determine the Most Effective Intervention for Hemorrhage Control Readiness for Laypersons: The PATTS Trial

NCT03479112 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 562

Last updated 2018-03-29

No results posted yet for this study

Summary

This is a randomized controlled study evaluating the ability of laypersons to correctly apply a tourniquet using different instructional methods. There are four arms being evaluated: flashcards, audio-kit with visual aids, formal in person Bleeding Control Basic (B-Con) course, and a control arm. All participants will then undergo B-Con training at the end of each session and then participants will be evaluated within a 3-6 month time period to evaluate their retention of knowledge and skills taught by the B-Con course.

Conditions

  • Traumatic Hemorrhage

Interventions

BEHAVIORAL

Flashcards

Participants will be provided with Flashcards depicting how to correctly apply a tourniquet to an extremity wound.

BEHAVIORAL

Audio-kit

Participants will be provided with an audio-kit with accompanying visual cues describing and depicting how to correctly apply a tourniquet to an extremity wound.

BEHAVIORAL

B-Con training

Participants will undergo the Bleeding control for the injured (B-Con) basic course.

BEHAVIORAL

B-Con training retention

Evaluation of retention of Bleeding Control for the injured basic course

Sponsors & Collaborators

  • The Gillian Reny Stepping Strong Center for Trauma Innovation

    collaborator UNKNOWN

  • Gillette Children's Specialty Healthcare

    collaborator OTHER

  • Brigham and Women's Hospital

    lead OTHER

Principal Investigators

  • Eric Goralnick, MD, MS · Brigham and Women's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-05-22
Primary Completion
2018-01-30
Completion
2018-01-30

Countries

  • United States

Study Locations

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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 NCT03479112 on ClinicalTrials.gov