Simulation-Based Study of Adding Video Communication to Dispatch Instruction

This study has been completed.
Sponsor:
Information provided by:
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT00564616
First received: November 26, 2007
Last updated: NA
Last verified: November 2007
History: No changes posted

November 26, 2007
November 26, 2007
April 2007
Not Provided
quality of chest compressions and rescue breaths [ Time Frame: every 30 seconds ]
Same as current
No Changes Posted
spent time to first effective chest compression and rescue breath [ Time Frame: expressed as seconds ]
Same as current
Not Provided
Not Provided
 
Simulation-Based Study of Adding Video Communication to Dispatch Instruction
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

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.

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.

Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Cardiac Arrest
Device: video cell phone
the "voice group" received voice CPR instruction via a voice-only cell phone, and the "video group" received interactive voice and video instruction via a video cell phone
  • Placebo Comparator: voice group
    the "voice group" received voice CPR instruction via a voice-only cell phone
    Intervention: Device: video cell phone
  • Experimental: video group
    the "video group" received interactive voice and video instruction via a video cell phone
    Intervention: Device: video cell phone

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
96
October 2007
Not Provided

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.
Both
16 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT00564616
200708079R
Yes
Not Provided
National Taiwan University Hospital
Not Provided
Study Director: Matthew Huei-Ming Ma, MD, PhD National Taiwan University Hospital
National Taiwan University Hospital
November 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP