Simulation-Based Study of Adding Video Communication to Dispatch Instruction
Primary Purpose
Cardiac Arrest
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
video cell phone
Sponsored by
About this trial
This is an interventional treatment trial for Cardiac Arrest focused on measuring cardiac arrest, video cell phone, dispatcher-assisted CPR
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.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
voice group
video group
Arm Description
the "voice group" received voice CPR instruction via a voice-only cell phone
the "video group" received interactive voice and video instruction via a video cell phone
Outcomes
Primary Outcome Measures
quality of chest compressions and rescue breaths
Secondary Outcome Measures
spent time to first effective chest compression and rescue breath
Full Information
NCT ID
NCT00564616
First Posted
November 26, 2007
Last Updated
November 26, 2007
Sponsor
National Taiwan University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00564616
Brief Title
Simulation-Based Study of Adding Video Communication to Dispatch Instruction
Official Title
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
Study Type
Interventional
2. Study Status
Record Verification Date
November 2007
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
October 2007 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
National Taiwan University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrest
Keywords
cardiac arrest, video cell phone, dispatcher-assisted CPR
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
96 (Actual)
8. Arms, Groups, and Interventions
Arm Title
voice group
Arm Type
Placebo Comparator
Arm Description
the "voice group" received voice CPR instruction via a voice-only cell phone
Arm Title
video group
Arm Type
Experimental
Arm Description
the "video group" received interactive voice and video instruction via a video cell phone
Intervention Type
Device
Intervention Name(s)
video cell phone
Intervention Description
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
Primary Outcome Measure Information:
Title
quality of chest compressions and rescue breaths
Time Frame
every 30 seconds
Secondary Outcome Measure Information:
Title
spent time to first effective chest compression and rescue breath
Time Frame
expressed as seconds
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthew Huei-Ming Ma, MD, PhD
Organizational Affiliation
National Taiwan University Hospital
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
17224230
Citation
Cheung S, Deakin CD, Hsu R, Petley GW, Clewlow F. A prospective manikin-based observational study of telephone-directed cardiopulmonary resuscitation. Resuscitation. 2007 Mar;72(3):425-35. doi: 10.1016/j.resuscitation.2006.07.025. Epub 2007 Jan 16.
Results Reference
background
PubMed Identifier
18583016
Citation
Yang CW, Wang HC, Chiang WC, Chang WT, Yen ZS, Chen SY, Ko PC, Ma MH, Chen SC, Chang SC, Lin FY. Impact of adding video communication to dispatch instructions on the quality of rescue breathing in simulated cardiac arrests--a randomized controlled study. Resuscitation. 2008 Sep;78(3):327-32. doi: 10.1016/j.resuscitation.2008.03.232. Epub 2008 Jun 25.
Results Reference
derived
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Simulation-Based Study of Adding Video Communication to Dispatch Instruction
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