Clinical Trials Directory

Trials / Completed

CompletedNCT03807206

Resuscitation Outcomes in the Netherlands Flashmob Questionnaire

Resucitation Outcomes in the Netherlands: Flash Mob Research on the Subject of Patient Experiences Regarding Do Not Resuscitate Orders.

Status
Completed
Phase
Study type
Observational
Enrollment
1,136 (actual)
Sponsor
Erasmus Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

Rationale: In-hospital cardiac arrest, associated with a survival to discharge of 15.0%, results in a good neurologic discharge in 9.1% - 30.0% of patients. Therefore it is recommended to engage in advanced care planning with patients, to discuss do-not-resuscitate (DNR) directives. In current knowledge, there are no published data about the prevalence of these DNR orders and associated factors in hospitalized patients in the Netherlands. Also, the conversation about DNR are sometimes perceived as awkward or untimely by patients. Objective: The primary goal is to estimate prevalence DNR order in Dutch hospitals. A secondary goal is to assess what geographical, patient and disease factors are associated with DNR status. Furthermore patient experience in the conversation leading to DNR-orders is of interest. Study design: A cross-sectional point prevalence study, in 10 participating hospitals of the ROUTiNE project. Study population: Patients who plan to be admitted for more than 24 hours to the participating hospitals, aged 18 or older, who are responsive and conscious. Main study parameters/endpoints: The prevalence of DNR orders, expressed as number per 1000 beds. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: There is no risk. Only one ten-minute interview per participant. Therefore the benefit of this study (as described in the objectives) outweigh the potential risks.

Conditions

Interventions

TypeNameDescription
BEHAVIORALQuestionnairePatient questionnaire

Timeline

Start date
2019-01-01
Primary completion
2019-02-07
Completion
2019-02-07
First posted
2019-01-16
Last updated
2019-07-16

Locations

12 sites across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT03807206. Inclusion in this directory is not an endorsement.