Resuscitation Outcomes in the Netherlands Flashmob Questionnaire
ROUTINE-F
Resucitation Outcomes in the Netherlands: Flash Mob Research on the Subject of Patient Experiences Regarding Do Not Resuscitate Orders.
1 other identifier
observational
1,136
1 country
12
Brief Summary
The aim of this study is to gain insight in patients' experiences regarding do not resuscitate conversations and decisions. A multicentre flash mob investigation will be conducted in which data will be obtained over the course of two weeks using electronic questionnaires that patients will fill out. General demographic data and a brief quality of life assessment (EQ-5D) will be collected. Whether a DNR converstation has taken place will be noted, along with patients' experiences with this conversation. Lastly the patient will be asked about his/her expectations of survival after cardiopulmonary resuscitation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2019
Shorter than P25 for all trials
12 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2019
CompletedFirst Submitted
Initial submission to the registry
January 7, 2019
CompletedFirst Posted
Study publicly available on registry
January 16, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 7, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
February 7, 2019
CompletedJuly 16, 2019
July 1, 2019
1 month
January 7, 2019
July 14, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Prevalence of DNR-orders
Percentage of DNR-orders in the total cohort as noted in the electronic patient file
1 day
Secondary Outcomes (4)
DNR-order discussion prevalence
1 day
DNR-order discussion experience
1 day
DNR-order discrepancy
1 day
Quality of life
1 day
Other Outcomes (1)
General demographic data
1 day
Study Arms (1)
Flashmob 2019
Patients from the following hospitals will receive a questionnaire/structured intereview: Erasmus MC, Franciscus Gasthuis \& Vlietland, Ikazia, Haaglanden Medisch Centrum, Albert Schweitzer ziekenhuis, Jeroen Bosch ziekenhuis, Rijnstate ziekenhuis, Amphia ziekenhuis, Tergooi klinieken, Medisch Spectrum Twente, Reinier de Graaf gasthuis. Pending: Maasstad ziekenhuis
Interventions
Eligibility Criteria
The base population consists of all adult patients admitted to all the participating hospitals. These consist of one academic centre and 10 general hospitals. The sampling is based on non-probability as it does not represent the entire population (i.e. inhabitants of the Netherlands), however it is based on probability sampling when the population is solely patients admitted to hospital.
You may qualify if:
- All patients admitted to the participating hospitals with a planned admission \>24 hours at the moment this study takes place.
You may not qualify if:
- Refusal to participate
- \<18 years of age
- Admitted in outpatient clinic and day treatment centres (e.g. haemodialysis)
- Admitted \<24 hours, as defined by not sleeping overnight in hospital
- No reliable proxy in the following situations:
- Unable to answer questions (e.g. unconscious, cognitively impaired, delirious)
- Language barrier (with no interpreter or family member)
- The following hospital departments are excluded:
- Intensive care unit
- Coronary/acute cardiac care unit
- Obstetrics
- Paediatrics
- Stroke unit
- Dialysis (outpatient dialysis)
- Day-care wards/short-stay (i.e. \<1 day)
- +1 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Erasmus Medical Centerlead
- European Society of Anaesthesiologycollaborator
Study Sites (12)
Jeroen Bosch ziekenhuis
's-Hertogenbosch, Netherlands
Rijnstate
Arnhem, Netherlands
Amphia
Breda, Netherlands
Reinier de Graaf gasthuis
Delft, Netherlands
Albert Schweitzer ziekenhuis
Dordrecht, Netherlands
Medisch Spectrum Twente
Enschede, Netherlands
Tergooi ziekenhuizen
Hilversum, Netherlands
Erasmus MC
Rotterdam, 3015CE, Netherlands
Franciscus Gasthuis & Vlietland
Rotterdam, Netherlands
Ikazia
Rotterdam, Netherlands
Maasstad
Rotterdam, Netherlands
Haaglanden Medisch Centrum
The Hague, Netherlands
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Robert Jan Stolker, MD PhD
Erasmus Medical Center
- PRINCIPAL INVESTIGATOR
Monique van Dijk, MD PhD
Erasmus Medical Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principal investigator/medical doctor
Study Record Dates
First Submitted
January 7, 2019
First Posted
January 16, 2019
Study Start
January 1, 2019
Primary Completion
February 7, 2019
Study Completion
February 7, 2019
Last Updated
July 16, 2019
Record last verified: 2019-07
Data Sharing
- IPD Sharing
- Will not share
Because of the personal nature of data (reg. age, sex, religion, eductional level) we will not make it available.