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Trial · NCT00539539

Automated Real-time Feedback on CPR Study

NCT00539539, Phase 2, Completed, University of Washington; results first posted 2012-06-25

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Automated Real-time Feedback on CPR Study. Trials, record NCT00539539. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00539539

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Automated Real-time Feedback on CPR Study
NCT number
NCT00539539
Status
Completed
Phases
Phase 2
Enrollment
1,586 participants, actual
Lead sponsor
University of Washington
Conditions
Heart Arrest
Interventions
Laerdal Q-CPR /technology
First posted
2007-10-04
Last updated
2012-06-25
Results first posted
2012-06-25
Limitations and caveats
Open label study - providers not blinded to intervention. High rates of missing CPR process measures.

Source ClinicalTrials.gov

Registered outcomes8

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryRate of ROSC During the Prehospital ResuscitationPrehospital resuscitationReturn of spontaneous circulation (ROSC)
SecondaryPulses Present at ED Arrival.Resuscitation
SecondarySurvival to Hospital DischargeLength of HospitalizationSurvival to hospital discharge
SecondaryCPR FractionUp to 10 minutes of CPRPercentage of time during CPR spend doing compressions.
SecondaryCompression DepthUp to 10 minutes of CPRAverage compression depth (mm) during the first 10 minutes of CPR.
SecondaryCompression RateUp to 10 minutes of CPRAverage compression rate during the first 10 minutes of CPR.
SecondaryPercentage of Compressions With an Incomplete ReleaseUp to 10 minutes of CPRPercentage of compressions with incomplete release during the first ten minutes of CPR.
SecondaryVentilation RateUp to 10 minutes of CPRAverage ventilation rate (breaths/minute) during the first ten minutes of CPR.

Outcomes8

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYRate of ROSC During the Prehospital ResuscitationPrehospital resuscitationIntent to treatParticipantsNUMBER
SECONDARYPulses Present at ED Arrival.ResuscitationIntention to treat. Presence of pulses not known for one participant on the feedback off arm. Analysis includes 815 participants on the feedback on arm and 770 on the feedback off arm.ParticipantsNUMBER
SECONDARYSurvival to Hospital DischargeLength of HospitalizationIntention to treat, with survival to hospital discharge missing for one participant on the feedback off arm. Analysis included 815 participants on the feedback on arm, and 770 on the feedback off arm.ParticipantsNUMBER
SECONDARYCPR FractionUp to 10 minutes of CPRIntention to treat, with CPR fraction available for 604 participants on the feedback on arm, and 570 on the feedback off arm.PercentageMEAN
SECONDARYCompression DepthUp to 10 minutes of CPRIntention to treat. Compression depth available for 529 participants on the feedback on arm and 467 on the feedback off arm.mmMEAN
SECONDARYCompression RateUp to 10 minutes of CPRIntention to treat. Average compression rate available for 604 participants on the feedback on arm and 570 on the feedback off arm.Compressions per minuteMEAN
SECONDARYPercentage of Compressions With an Incomplete ReleaseUp to 10 minutes of CPRIntention to treat. Incomplete release available for 529 participants on the feedback on arm and 467 on the feedback off arm.% of compressions w/ incomplete releaseMEAN
SECONDARYVentilation RateUp to 10 minutes of CPRIntention to treat. Ventilation rate available in 347 participants on the feedback on arm and 346 on the feedback off arm.breaths per minuteMEAN

Results by group16

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Rate of ROSC During the Prehospital ResuscitationFeedback On361Participants
Rate of ROSC During the Prehospital ResuscitationFeedback Off345Participants
Pulses Present at ED Arrival.Feedback On260Participants
Pulses Present at ED Arrival.Feedback Off243Participants
Survival to Hospital DischargeFeedback On92Participants
Survival to Hospital DischargeFeedback Off96Participants
CPR FractionFeedback On66Standard Error 1Percentage
CPR FractionFeedback Off64Standard Error 1Percentage
Compression DepthFeedback On39.6Standard Error 0.4mm
Compression DepthFeedback Off37.8Standard Error 0.4mm

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDFeedback On815
Overall StudySTARTEDFeedback Off771
Overall StudyCOMPLETEDFeedback On815
Overall StudyCOMPLETEDFeedback Off771
Overall StudyNOT COMPLETEDFeedback On0
Overall StudyNOT COMPLETEDFeedback Off0

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityFeedback On
Total, all-cause mortalityFeedback Off
Total, other adverse eventsFeedback On0815
Total, other adverse eventsFeedback Off0771
Total, serious adverse eventsFeedback On0815
Total, serious adverse eventsFeedback Off0771

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
21296838DERIVED

Source PubMed

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
U01HL077863Resuscitation Outcomes Consortium (ROC) Data Coordinating CenterMAY, SUSANNEUNIVERSITY OF WASHINGTONNATIONAL HEART, LUNG, AND BLOOD INSTITUTE2004 to 2015

Trial comparisons4

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Feedback On vs Feedback Off: Survival to Hospital DischargeTrial comparisons
Feedback On vs Feedback Off: Rate of ROSC During the Prehospital ResuscitationTrial comparisons
Feedback On vs Feedback Off: Pulses Present at ED Arrival.Trial comparisons
Feedback On vs Feedback Off: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00539539

GET https://conductscience.org/api/trials/v1/NCT00539539/registered