Trial Outcomes & Findings for MIHS Emergency Department CPR Quality Improvement Project (NCT NCT01245699)

NCT ID: NCT01245699

Last Updated: 2019-04-26

Results Overview

Measurement of chest compression depth

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

115 participants

Primary outcome timeframe

during CPR

Results posted on

2019-04-26

Participant Flow

Participant milestones

Participant milestones
Measure
Before Training, RTAV CPR Feedback and Debriefing
Before scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
After Training, RTAV CPR Feedback, and Debriefing
After scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing.
Overall Study
STARTED
61
54
Overall Study
COMPLETED
52
49
Overall Study
NOT COMPLETED
9
5

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

MIHS Emergency Department CPR Quality Improvement Project

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Phase I
n=52 Participants
Before training
Phase 2
n=49 Participants
After training.
Total
n=101 Participants
Total of all reporting groups
Age, Customized
Mean Age of participants
56 years
n=5 Participants
60 years
n=7 Participants
58 years
n=5 Participants
Sex: Female, Male
Female
19 Participants
n=5 Participants
8 Participants
n=7 Participants
27 Participants
n=5 Participants
Sex: Female, Male
Male
33 Participants
n=5 Participants
41 Participants
n=7 Participants
74 Participants
n=5 Participants

PRIMARY outcome

Timeframe: during CPR

Measurement of chest compression depth

Outcome measures

Outcome measures
Measure
Before Training
n=52 Participants
Before scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
After Training.
n=49 Participants
After scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
CPR Quality-compression Depth
46.7 mm
Interval 42.9 to 50.5
61.6 mm
Interval 58.7 to 64.4

PRIMARY outcome

Timeframe: during CPR

Percent of Chest Compressions greater than 51mm

Outcome measures

Outcome measures
Measure
Before Training
n=52 Participants
Before scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
After Training.
n=49 Participants
After scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
CPR Quality-percent of >51mm Compressions
30.6 percentage of chest compressions >51mm
Interval 18.3 to 42.9
87.4 percentage of chest compressions >51mm
Interval 74.6 to 100.1

PRIMARY outcome

Timeframe: during CPR

Chest Compression Release Velocity

Outcome measures

Outcome measures
Measure
Before Training
n=52 Participants
Before scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
After Training.
n=49 Participants
After scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
CPR Quality
314 mm/s
Interval 289.0 to 338.0
442 mm/s
Interval 422.0 to 462.0

PRIMARY outcome

Timeframe: During CPR

Chest Compression Fraction indicating the percentage of time in which chest compressions are done by rescuers during a cardiac arrest

Outcome measures

Outcome measures
Measure
Before Training
n=52 Participants
Before scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
After Training.
n=49 Participants
After scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
CPR Quality-compression Fraction
84.3 % of time chest compressions are done
Interval 80.8 to 87.7
88.4 % of time chest compressions are done
Interval 84.8 to 91.9

PRIMARY outcome

Timeframe: During CPR

Mean Chest Compression Rate

Outcome measures

Outcome measures
Measure
Before Training
n=52 Participants
Before scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
After Training.
n=49 Participants
After scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
CPR Quality-Chest Compression Rate
125 CCs/min
Interval 122.0 to 128.0
125 CCs/min
Interval 122.0 to 127.0

PRIMARY outcome

Timeframe: During CPR

Pre-shock pause: time from cessation of CPR to shock delivery

Outcome measures

Outcome measures
Measure
Before Training
n=52 Participants
Before scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
After Training.
n=49 Participants
After scenario-based training, real-time audiovisual CPR feedback, and post-event debriefing
CPR Quality- Pre-shock Pause
9.7 sec
Interval 3.0 to 16.3
5.9 sec
Interval 0.0 to 13.9

Adverse Events

Phase I

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Phase 2

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Bentley J Bobrow, MD

Maricopa Integrated Health System

Phone: 602-364-0580

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place