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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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00564616
Enrollment
96
Registered
2007-11-28
Start date
2007-04-30
Completion date
2007-10-31
Last updated
2007-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest

Keywords

cardiac arrest, video cell phone, dispatcher-assisted CPR

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.

Interventions

DEVICEvideo 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

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frame
quality of chest compressions and rescue breathsevery 30 seconds

Secondary

MeasureTime frame
spent time to first effective chest compression and rescue breathexpressed as seconds

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026