Skip to main content
Clinical Trials/NCT01191736
NCT01191736
Completed
Not Applicable

Comparison of the Effectiveness of Ultra-Brief and Brief Hands-Only CPR Video Training With and Without Psychomotor Skill Practice for Lay Responders: a Controlled Randomized Study

Valleywise Health0 sites336 target enrollmentSeptember 2009
ConditionsCardiac Arrest

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Arrest
Sponsor
Valleywise Health
Enrollment
336
Primary Endpoint
Median Compression Depth (mm)
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

Bystander CPR improves survival from Out of Hospital Cardiac Arrest. This study examines the efficacy of ultra-brief video training for Hands-Only CPR. Subjects were randomized to one of four training conditions, then assessed for CPR skills retention.

Detailed Description

Bystander CPR improves survival from Out of Hospital Cardiac Arrest. This study is the first of its kind to examine the efficacy of ultra-brief video training for Hands-Only CPR without the use of a manikin. The results will inform future efforts to mass train citizens in CPR. Subjects were randomized to one of four training conditions, then assessed for CPR skills retention. The four groups were 1) no training; 2) ultra-brief training video (90 seconds); 3) short training video (5 minutes) with no practice; and 4) short training video with hands-on practice. The subjects were then evaluated for CPR skills retention. One half of the subjects were evaluated on the training day, and the other half were evaluated two months later.

Registry
clinicaltrials.gov
Start Date
September 2009
End Date
November 2009
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Members of a local area church

Exclusion Criteria

  • Less than 18 years old
  • formal CPR training or certification within last 2 years
  • Lacks fluency in English
  • Works as a health care provider

Outcomes

Primary Outcomes

Median Compression Depth (mm)

Time Frame: 60 minutes after intervention or two months after intervention

Assessment of resuscitation skills using a Laerdal Resusci Annie recording manikin and Laerdal PC Skill Reporting software

Secondary Outcomes

  • The Proportion of Subjects Who Assessed the Responsiveness of the Victim (Manikin) as Judged by Expert Raters(60 minutes after intervention and two months after intervention)

Similar Trials