Skip to main content
Clinical Trials/NCT00564616
NCT00564616
Completed
Not Applicable

A Randomized Controlled Study Focused on Impact of Adding Video Communication to Dispatch Instruction on the Quality of CPR, Including Chest Compressions and Rescue Breaths, in Simulated Cardiac Arrests

National Taiwan University Hospital0 sites96 target enrollmentApril 2007
ConditionsCardiac Arrest

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Arrest
Sponsor
National Taiwan University Hospital
Enrollment
96
Primary Endpoint
quality of chest compressions and rescue breaths
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

The purpose of this study is to determine whether adding interactive video communication to dispatch instruction improves the quality of bystander cardiopulmonary resuscitation in simulated cardiac arrests.

Detailed Description

Sudden cardiac death (SCD) is a leading cause of adult death and bystander cardiopulmonary resuscitation (CPR) significantly improves survival. Dispatch assistance increases the chance of bystander CPR but the quality of dispatcher-assisted CPR (DA-CPR) remains unsatisfactory. This study is conducted to assess the effect of adding interactive video communication to dispatch instruction on the quality of bystander CPR, including chest compressions and rescue breathing, in simulated cardiac arrests.

Registry
clinicaltrials.gov
Start Date
April 2007
End Date
October 2007
Last Updated
18 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Volunteers above 16 years of age who have not received any CPR training within the last 5 years were recruited.

Exclusion Criteria

  • Healthcare providers, non-Mandarin speaking individuals, and those with illness/physical conditions that prevent them from receiving telephone instructions or performing CPR were excluded.

Outcomes

Primary Outcomes

quality of chest compressions and rescue breaths

Time Frame: every 30 seconds

Secondary Outcomes

  • spent time to first effective chest compression and rescue breath(expressed as seconds)

Similar Trials