A Mannequin Study to Assess Various CPR Training Methods Using a Student Population

Sponsor
University of Pennsylvania (Other)
Overall Status
Completed
CT.gov ID
NCT01833910
Collaborator
(none)
25
1
4
24
1

Study Details

Study Description

Brief Summary

Prompt delivery of cardiopulmonary resuscitation (CPR) can double a victims chance of survival from cardiac arrest (CA), yet it is provided in less than 1/3 of witnessed events. Studies indicate that video-based education methods can effectively train bystanders in CPR. Using the education and evaluation methods of an existing in-hospital training program, the investigators will assess the CPR skills of students taught with video-only methods, with and without psychomotor skills practice, and compare them to those using a video self-instruction (VSI) kit.

Condition or Disease Intervention/Treatment Phase
  • Other: AHA CPR Anytime Video Self-Instruction Kit
  • Other: AHA CPR Anytime DVD
N/A

Detailed Description

The long term goal of our work is to implement real world CPR training strategies that maximize resuscitation skill retention, and promote willingness to act while addressing major barriers to training including time and cost. To accomplish this, the study team will train student volunteers from the University of Pennsylvania using one of three methods: 1) a video-only method with no psychomotor skill practice, 2) a video-only method with psychomotor skill practice on a household object or 3) a video self-instruction (VSI) kit. Volunteers will be young, healthy students from the University of Pennsylvania with no CPR Training within the last 24 months. The investigators will use the American Heart Association's CPR Anytime Video Self-Instruction Kit which comes equipped with a DVD and inflatable manikin.

For the groups receiving the Video-Only methods, the investigators will remove the inflatable manikin and train the subjects with the DVD. The investigators will randomize the participants to one of the video-only methods or to the VSI kit method of training when they are scheduled for training. Immediately following the training, the investigators will conduct a CPR skills test to measure the effectiveness of the training method. Three (3) to twelve (12) months post-training the investigators will schedule and conduct an in-person interview with subjects. As part of the interview, subjects will be asked to complete a survey measuring their comfort level and willingness to use their CPR skills. Subjects will also be asked to complete another CPR Skills test.

Study Design

Study Type:
Interventional
Actual Enrollment :
25 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
A Mannequin Study to Assess Various CPR Training Methods Using a Student Population
Study Start Date :
Oct 1, 2012
Actual Primary Completion Date :
Apr 1, 2013
Actual Study Completion Date :
Oct 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Video-only - DVD

CPR Training with AHA CPR Anytime DVD presented on a TV with DVD player and no psychomotor skill practice.

Other: AHA CPR Anytime DVD
A CPR Training Video, originally developed as part of a kit, administered without the accompanying manikin.

Experimental: Video-only - iPad

CPR Training with AHA CPR Anytime DVD presented on a portable video player and no psychomotor skill practice.

Other: AHA CPR Anytime DVD
A CPR Training Video, originally developed as part of a kit, administered without the accompanying manikin.

Experimental: Video-only with Household Object

CPR Training with AHA CPR Anytime DVD and practice on a household item

Other: AHA CPR Anytime DVD
A CPR Training Video, originally developed as part of a kit, administered without the accompanying manikin.

Experimental: Video Self Instruction Kit

CPR Training with AHA CPR Anytime Video Self-Instruction kit including manikin

Other: AHA CPR Anytime Video Self-Instruction Kit
CPR Training utilizing a video self-instruction kit including training video and inflatable manikin.

Outcome Measures

Primary Outcome Measures

  1. CPR Compression Quality [3 months post training]

    CPR Compression rate and depth measured on a skill reporting CPR manikin during a simulated cardiac emergency.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Must be able to complete 25-30 minutes of moderate physical activity
Exclusion Criteria:
  • CPR Training within the past 24 months

Contacts and Locations

Locations

Site City State Country Postal Code
1 Center for Resusciation Science - Univerity of Pennsylvania Philadelphia Pennsylvania United States 19104

Sponsors and Collaborators

  • University of Pennsylvania

Investigators

  • Principal Investigator: Benjamin Abella, MD, MPhil, University of Pennsylvania

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of Pennsylvania
ClinicalTrials.gov Identifier:
NCT01833910
Other Study ID Numbers:
  • 816764
First Posted:
Apr 17, 2013
Last Update Posted:
Nov 1, 2018
Last Verified:
Oct 1, 2018
Keywords provided by University of Pennsylvania
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 1, 2018