This trial is active, not recruiting.

Condition cardiac arrest
Treatment telephone simulation training
Sponsor University of Washington
Collaborator Agency for Healthcare Research and Quality (AHRQ)
Start date September 2013
End date July 2016
Trial size 212 participants
Trial identifier NCT01972087, 44640-EJ, 5R18HS021658-02


This study is to test the use of simulation training to improve 9-1-1 telecommunicators' call processing and response. Training sessions will expose 9-1-1 telecommunicators to several realistic emergency situations through mock 9-1-1 calls with a trained actor playing the part of a reporting party, followed immediately by feedback on call handling provided by a trained call observer. Investigators hypothesize that simulation followed by trained observer-directed feedback will increase correct triage of medical emergency and delivery of pre-arrival instructions during simulated calls and in actual 9-1-1 calls.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification efficacy study
Intervention model single group assignment
Masking open label
Primary purpose health services research
(No Intervention)
Participants randomized to the control arm receive no telephone simulation training.
Participants randomized to the intervention arm receive telephone simulation training.
telephone simulation training
The intervention consists of four 20-minute telephone simulation training sessions over a 4 month period (one session each month). Each 20-minute training session will include 3 simulated 9-1-1 calls, performed by a standardized caller (trained actor) and feedback will be provided right away by a trained observer who takes notes during the simulation calls and discusses the teaching points after the session. In total, the 9-1-1 dispatchers will receive 12 different simulated calls.

Primary Outcomes

Change in elapsed seconds from call answer to start of telephone-cardiopulmonary resuscitation (T-CPR) instructions in cardiac arrest calls in simulations and in actual calls.
time frame: Once monthly over 4 months (during simulations); at event (actual cardiac arrest 9-1-1 call) over 12 months.

Secondary Outcomes

Change in proportion of calls with querying behaviors compliant with the "all-callers" interviewing protocol.
time frame: Once monthly over 4 months (during simulations); at event (actual cardiac arrest 9-1-1 call) over 12 months.

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: 9-1-1 call-center call receivers. - Exclusion Criteria:

Additional Information

Official title Simulation Training to Improve 911 Dispatcher Identification of Cardiac Arrest
Principal investigator Hendrika Meischke, PhD
Trial information was received from ClinicalTrials.gov and was last updated in October 2015.
Information provided to ClinicalTrials.gov by University of Washington.