COMPLETED

Mixed-reality REBOA Simulator With Virtual Coaching

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) is a life-saving emergency procedure that is highly suited for simulation-based training. This study aims to assess the validity of our REBOA simulator with virtual coach (or live quantitative feedback) for mastery learning. The hypotheses are: H0: Virtual coach is non-inferior in REBOA training to an average human instructor. H1: Virtual coach is inferior in REBOA training to an average human instructor. We expect to learn whether the virtual coach is non-inferior to an average human instructor for US-guided REBOA training. Additionally, we expect to find which determinants affect success rate most and to assess the needs for the current simulator system's future software development.

Official Title

Assessment of a Mixed-reality Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) Training Simulator With Virtual Coach for Mastery Learning.

Quick Facts

Study Start:2022-02-10
Study Completion:2022-11-11
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05062928

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * \>18 years of age
  1. * i. not obtaining informed consent,
  2. * ii. inability to complete all the procedures,
  3. * iii. Completed a REBOA course iv. Used the US-guided REBOA simulator in any way

Contacts and Locations

Principal Investigator

Samsun Lampotang
STUDY_DIRECTOR
Univeristy of Florida

Study Locations (Sites)

University of Florida
Gainesville, Florida, 32601
United States

Collaborators and Investigators

Sponsor: University of Florida

  • Samsun Lampotang, STUDY_DIRECTOR, Univeristy of Florida

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-02-10
Study Completion Date2022-11-11

Study Record Updates

Study Start Date2022-02-10
Study Completion Date2022-11-11

Terms related to this study

Keywords Provided by Researchers

  • aorta, abdominal
  • aorta, thoracic
  • Teaching

Additional Relevant MeSH Terms

  • Hemorrhage
  • Simulation Training