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
| 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
| 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 CPRMeasurement of chest compression depth
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 CPRPercent of Chest Compressions greater than 51mm
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 CPRChest Compression Release Velocity
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 CPRChest Compression Fraction indicating the percentage of time in which chest compressions are done by rescuers during a cardiac arrest
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 CPRMean Chest Compression Rate
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 CPRPre-shock pause: time from cessation of CPR to shock delivery
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
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place