Stress, Psychological Clinical Trial
— NG911Official title:
Multi-tasking to Hyper-tasking: Investigating the Impact of Next Generation 911
Verified date | May 2018 |
Source | University of Washington |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Emergency call centers across the country are preparing for the Next Generation 911 (NG911)
initiative, which will allow citizens to place 9-1-1 "calls" using digital technologies such
as text messaging, email, Skype or instant messaging, and will expand emergency information
sources to also include streaming video, photo uploads, and automatic crash notifications.
The impact of these new information and communication technologies on those tasked with using
them in time-sensitive emergency situations is unknown. Our study is designed to address the
following hypotheses: 1) We hypothesize that NG911 implementation will have a significant
effect on telecommunicator stress levels and 2) A resiliency training tailored to the needs
of telecommunicators will mitigate the impact on NG911 implementation on stress levels. We
will test these hypotheses through the following specific aims:
Aim 1: Measure levels of stress, job satisfaction and job performance among 9-1-1
telecommunicators before and after the NG911 implementation.
Aim 2: Develop and test the efficacy of an evidence-based resiliency training and worker
support intervention to improve psychological well-being and job performance of 9-1-1
telecommunicators.
Aim 3: Build an ABM tool of 9-1-1 call centers to improve 9-1-1 telecommunicator workforce
training and smooth transitions to future call center innovations.
Status | Completed |
Enrollment | 323 |
Est. completion date | December 15, 2017 |
Est. primary completion date | November 1, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: - subjects must be 9-1-1 telecommunicators (call receivers and dispatchers) who work at participating call centers and consent to participate. Exclusion Criteria: - We will exclude subjects who do not consent to participate - We will exclude subjects who do not confirm that they are 21 or older. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Washington |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Calgary Symptoms of Stress Inventory | Change in the Calgary Symptoms of Stress Inventory results | Baseline, immediately post intervention and 3 months post intervention |
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