Cardiopulmonary resuscitation (CPR) quality improvement programme

ISRCTN ISRCTN56583860
DOI https://doi.org/10.1186/ISRCTN56583860
Secondary identifying numbers PB-PG-1207-14246
Submission date
30/11/2010
Registration date
05/07/2011
Last edited
04/02/2016
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Circulatory System
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Gavin Perkins
Scientific

Warwick Medical School Clinical Trials Unit
University of Warwick
Coventry
CV4 7AL
United Kingdom

Email g.d.perkins@warwick.ac.uk

Study information

Study designMulticentre prospective cohort study
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Hospital
Study typeTreatment
Participant information sheet Not available in web format, please use the contact details below to request a patient information sheet.
Scientific titleCardiopulmonary resuscitation (CPR) quality improvement programme: a multicentre, prospective, cohort study
Study objectivesImplementing a CPR quality improvement initiative will improve the rate of return of spontaneous circulation and other outcomes in patients sustaining cardiac arrest
Ethics approval(s)Coventry Research Ethics Committee, 26/06/2009, REC ref: 09/H1210/65
Health condition(s) or problem(s) studiedIn-hospital cardiac arrests
Intervention1. Control
2. CPR feedback through Q-CPR® (Laerdal medical, UK)
3. CPR feedback through Q-CPR® (Laerdal medical, UK) plus team briefing / debriefing
Intervention typeOther
Primary outcome measureSurvived event [defined as sustained (> 20 minutes) return of spontaneous circulation]
Secondary outcome measures1. Patient outcomes
1.1. Any return of spontaneous circulation
1.2. Survival to hospital discharge
1.3. Cerebral performance category of patients at discharge
2. Process outcomes
2.1. Quality of emergency calls
2.2. Chest compression depth, rate
2.3. No flow time
2.4. Duration of pre and post-shock pauses
2.5. Ventilation rate
2.6. time to first shock
2.7.Appropriate decision to shock
3. Team factors
3.1. CPR knowledge
3.2. Confidence / preparedness
Overall study start date01/11/2009
Completion date31/01/2013

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit18 Years
SexBoth
Target number of participants912
Key inclusion criteriaPatients have to be either 18 or older and suffer an in-hospital cardiac arrest where resuscitation is attempted (defined as loss of a pulse requiring the delivery of chest compressions).
Key exclusion criteria1. Patient has a Do-not-attempt resuscitation order written and documented in their medical records
2. Cardiac arrest not attended by a resuscitation team
3. Out - of - hospital cardiac arrest
4. Previous participation in this study
Date of first enrolment01/11/2009
Date of final enrolment31/01/2013

Locations

Countries of recruitment

  • England
  • United Kingdom

Study participating centre

Warwick Medical School Clinical Trials Unit
Coventry
CV4 7AL
United Kingdom

Sponsor information

Heart of England NHS Foundation Trust (UK)
Hospital/treatment centre

c/o Elizabeth Adey
R+D Manager
MIDRU
Bordesley Green East
Birmingham
B9 5SS
England
United Kingdom

Email Elizabeth.Adey@heartofengland.nhs.uk

Funders

Funder type

Government

National Institute for Health Research (NIHR) (UK) - Research for Patient Benefit (RfPB) programme (PB-PG-1207-14246)

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Protocol article protocol 18/10/2011 Yes No
Results article results 01/11/2015 Yes No

Editorial Notes

04/02/2016: Publication reference added.