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Enrolling By Invitation
NCT05695469
The Impact of ResuGlove as a Chest Compression Feedback Device
Conditions: Testing, Reality
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Phase: NA
Enrollment: 30
Sponsor: University of Turku
Location: Finland
Summary
The goal of this simulation-based randomized trial is to assess if the newly proposed ResuGlove can improve the quality of chest compressions during CPR training of laypersons and inexperienced health professionals.
The main questions it aims to answer are:To determine if the newly developed wearable resuscitation gloves will improve the quality of chest compression during simulation-based CPR trainingTo determine the learnability and usability of the ResuGlove using the System Usability Scale (SUS) questionnaireParticipants will be randomly assigned into two equal groups the ResuGlove group (group 1) vs the traditional CPR group (Group 2).
The investigators will compare the quality of chest compression between these two groups.
On the same day, participants will be asked about the learnability and usability of ResuGlove using the System Usability Scale (SUS questionnaire.
Eligibility Criteria
Inclusion Criteria:First-year, second-year or third-year medical student at the University of TurkuStudents must have previous basic life support trainingParticipants should be able to understand and communicate in EnglishExclusion Criteria:Participants must not have previous advance cardiac life support training.Participants who are not able to understand and communicate in EnglishStudents with known cardiac/pulmonary diseases, back pain, and wrist problems
Source: ClinicalTrials.gov (NCT05695469). StuddyBuddy aggregates publicly available trial information.