Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12616001392459
Ethics application status
Approved
Date submitted
7/09/2016
Date registered
7/10/2016
Date last updated
26/04/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
Pilot assessment of the utility and acceptability of a new ‘goals of care and not for cardiopulmonary resuscitation’ documentation tool/form
Scientific title
Pilot assessment of the utility of and acceptability to emergency department doctors of a new 'goals of care and not for cardiopulmonary resuscitation' documentation tool/form at Cabrini Emergency Department for use in all patients requiring a goals of care discussion as determined by their emergency department doctor during the study period.
Secondary ID [1] 289999 0
nil
Universal Trial Number (UTN)
U1111-1186-8231
Trial acronym
n/a
Linked study record

Health condition
Health condition(s) or problem(s) studied:
End of life care 300008 0
Condition category
Condition code
Public Health 299903 299903 0 0
Health service research

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
See attached form for the intervention. This is a form that can be utilised by physicians to document conversations with patients and families about end of life management plans.

This form will replace the usual not for CPR (cardiopulmonary resuscitation) form currently utilised at Cabrini hospital. All current forms will be replaced in the Emergency Department for the duration of the study by the new form that is being studied. Forms will not be replaced in other locations in the Cabrini network.

Doctors will receive face-to-face and email education about the new form in the two weeks preceding the intervention. The education will be delivered by an emergency physician (KW) in the emergency department face-to-face and will be a 5-10 minute conversation showing them the form and pointing out the sections available for use. The email will be similar, advising them that the usual forms will be replaced by the study forms with an attachment to the email including a copy of the form. There will be the opportunity for doctors to ask questions about the form face-to-face or via email. There are no educational tools other than the form, nor is there education in how to conduct a conversation about goals-of-care or resuscitation appropriateness/futility.

Only doctors will complete the forms and we anticipate using approximately 150 forms during a 12 week study period. Doctors are also able to document conversations in the regular medical notes if they prefer but there will be no other not for CPR forms available.

Adherence to using this form (rather than the usual not for CPR form) will be measured by retrospective review of all medical notes of patients enrolled in the study.

All doctors in the ED will receive an email with the trial form attached and a 500 word description of the aim of the study. One paragraph explanation for each of the sections to be completed will be provided. Doctors will be asked to time the conversations on their phones and enter the data at the bottom of the form.

See form attached to ANZCTR registration record for the intervention
Intervention code [1] 295705 0
Behaviour
Comparator / control treatment
Retrospective review of comparison group of patients (1 month before implementation). A group of patients matched for age/gender and SPICT status who were admitted from ED to the ward will be selected by research staff and Dr Katie Walker. The comparison group will be reviewed retrospectively for patient outcomes (length of stay; discharge or death) and evidence of discussion documentation (on the form and/or in the patient notes). The comparison group will also provide a baseline NFR rate.

The Supportive & Palliative Care Indicators tool (SPICT) will be used retrospectively to identify those patients admitted via ED who were at risk of dying within 12 months. The tool identifies evidence of general deteriorating health, as well as evidence of advance medical conditions to identify those patients at risk of dying, akin to the 'surprise question' (would you be surprised if this patient died in the next 12 months). Patients determined to be at risk are those for whom goals of care discussions should be conducted, and limitations of treatment considered.
Control group
Historical

Outcomes
Primary outcome [1] 299393 0
The attitudes to and experiences of doctors using the new form in the Emergency Department to document of end-of-life discussions, goals of care discussions and limits of treatment discussion and/or decisions.

This will be evaluated by surveys and semi-structured interviews with doctors, designed for this study (attached).

This is a composite outcome as the numbers of participants is small.
Timepoint [1] 299393 0
October 1st to November 30th 2016

Survey will be sent one week post intervention. Interviews 1-4 weeks post intervention.
Secondary outcome [1] 327030 0
Establishment of the average duration (in minutes) and standard deviation of end-of-life/goals of care discussions in Emergency patients at Cabrini Emergency Department

This will be measured by each physician completing a form estimating (or timing) the duration of the conversation and documenting this on the form.
Timepoint [1] 327030 0
October 1st to November 30th 2016

Documentation will be audited 1-4 weeks post intervention.
Secondary outcome [2] 327031 0
Evaluation of the utility of each section of the form to physicians as measured by the completion rate of each section of the form.

This will be retrospectively assessed by reviewing each study form and determining in a binary fashion, whether each section was utilised or not
Timepoint [2] 327031 0
October 1st to November 30th 2016

Documentation will be audited 1-4 weeks post intervention
Secondary outcome [3] 327543 0
To determine whether a form containing these end-of-life discussion sections, facilitates discussion with patients and their carers about these issues

This will be evaluated by surveys and semi-structured interviews with doctors and nursing staff, designed for this study (attached).
Timepoint [3] 327543 0
October 1st to November 30th 2016

Interviews will be conducted 1-4 weeks post intervention
Secondary outcome [4] 327544 0
To determine whether this form prompts decisions about setting treatment limits for patients (i.e. not for cardiopulmonary resuscitation)

This will be evaluated by semi-structured interviews with doctors
Timepoint [4] 327544 0
October 1st to November 30th 2016

Interviews will be conducted 1-4 weeks post intervention

Eligibility
Key inclusion criteria
Patients attending Cabrini Emergency Department between the time periods of October 1st to November 30th 2016 for whom an attending doctor determines that an end-of-life/goals of care discussion is appropriate.
All doctors who work in the Emergency Department are eligible to take part in the study.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
patients age less than 18 years
no exclusion criteria for doctors

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Nil
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Nil
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
All doctors attending the ED will be eligible for enrolment. All doctors wishing to document a Not for CPR decision will be required to utilise this form. The goals of care page is optional as are all sections individually within the form.

All forms will be sequentially numbered and a requirement of obtaining a form will be to provide the patient Universal Record number to the researchers to enable tracking of the patient records. Note that the form contains a research data entry space to record the estimated duration of the conversation and documentation of the discussion.

Doctors who use a form are eligible for semi-structured interview. All those using a form will approached face-to-face and by email to invite participation.

Interviews will be recorded and transcribed into NVivo. Data will be coded into themes and analysed by two researchers with experience in qualitative research. Any dissent will be reviewed by a third researcher. Interviews will continue until theme saturation is obtained.

The duration of consultations times will be analysed by simple descriptive statistics (mean, median, SD)

Retrospective medical review will be undertaken to determine the completion rate of each section of the form. Simple descriptive statistics will be used to analyse this data. (mean, median, SD)

No sample size calculations as this is a qualitative study. On prior experience we anticipate that at least two not-for-CPR documents are completed each day in the ED. Over a 12 week period, we anticipate that approximately 150 trial forms will be used and therefore each doctor is likely to complete at least 5 forms.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
18/10/2016
Actual
1/12/2016
Date of last participant enrolment
Anticipated
18/01/2017
Actual
28/02/2017
Date of last data collection
Anticipated
18/03/2017
Actual
28/08/2017
Sample size
Target
150
Accrual to date
Final
108
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 6537 0
Cabrini Hospital - Malvern - Malvern
Recruitment postcode(s) [1] 14118 0
3144 - Malvern

Funding & Sponsors
Funding source category [1] 294486 0
Hospital
Name [1] 294486 0
Cabrini Hospital
Country [1] 294486 0
Australia
Primary sponsor type
Individual
Name
Michele Levinson
Address
Cabrini-Monash University Department of Medicine
Cabrini Insitute
154 Wattletree Rd
Malvern
Vic
3144
Country
Australia
Secondary sponsor category [1] 293216 0
Individual
Name [1] 293216 0
Katie Walker
Address [1] 293216 0
Emergency Department
Cabrini Hospital
183 Wattletree Rd
Malvern
Vic
3144
Country [1] 293216 0
Australia
Other collaborator category [1] 279171 0
Individual
Name [1] 279171 0
Erin O'Callaghan
Address [1] 279171 0
Emergency Department
Cabrini Hospital
183 Wattletree Rd
Malvern
Vic
3144
Country [1] 279171 0
Australia
Other collaborator category [2] 279172 0
Individual
Name [2] 279172 0
Amber Mills
Address [2] 279172 0
Cabrini-Monash University Department of Medicine
Cabrini Institute
154 Wattletree Rd
Malvern
Vic
3144
Country [2] 279172 0
Australia
Other collaborator category [3] 279216 0
Individual
Name [3] 279216 0
Gaya Sritharan
Address [3] 279216 0
Cabrini-Monash University Department of Medicine
Cabrini Insitute
154 Wattletree Rd
Malvern
Vic
3144
Country [3] 279216 0
Australia
Other collaborator category [4] 279217 0
Individual
Name [4] 279217 0
Anthea Gellie
Address [4] 279217 0
Cabrini-Monash University Department of Medicine
Cabrini Institute
154 Wattletree Rd
Malvern
Vic
3144
Country [4] 279217 0
Australia
Other collaborator category [5] 279218 0
Individual
Name [5] 279218 0
Georgina Johnstone
Address [5] 279218 0
Cabrini-Monash University Department of Medicine
Cabrini Institute
154 Wattletree Rd
Malvern
Vic
3144
Country [5] 279218 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 295810 0
Cabrini Human Research Ethics committee
Ethics committee address [1] 295810 0
Ethics committee country [1] 295810 0
Australia
Date submitted for ethics approval [1] 295810 0
31/08/2016
Approval date [1] 295810 0
15/09/2016
Ethics approval number [1] 295810 0
CHREC 02-24-10-16

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes
Attachments [1] 1106 1106 0 0
/AnzctrAttachments/371357-Combined_discussion_NFCPR_form.pdf (Supplementary information)
Attachments [2] 1152 1152 0 0
/AnzctrAttachments/371357-Doctors Survey Questions.docx (Supplementary information)
Attachments [3] 1153 1153 0 0
/AnzctrAttachments/371357-Interview questions_final.docx (Supplementary information)
Attachments [4] 1154 1154 0 0
/AnzctrAttachments/371357-Nurses Survey Questions.docx (Supplementary information)
Attachments [5] 1155 1155 0 0
/AnzctrAttachments/371357-CHREC approval.pdf (Ethics approval)

Contacts
Principal investigator
Name 68486 0
A/Prof Michele Levinson
Address 68486 0
Cabrini-Monash University Department of Medicine
Cabrini Institute
154 Wattletree Rd
Malvern
Vic
3144
Country 68486 0
Australia
Phone 68486 0
+61 3 9508 3466
Fax 68486 0
Email 68486 0
[email protected]
Contact person for public queries
Name 68487 0
Michele Levinson
Address 68487 0
Cabrini-Monash University Department of Medicine
Cabrini Institute
154 Wattletree Rd
Malvern
Vic
3144
Country 68487 0
Australia
Phone 68487 0
+61 3 9508 3466
Fax 68487 0
Email 68487 0
[email protected]
Contact person for scientific queries
Name 68488 0
Michele Levinson
Address 68488 0
Cabrini-Monash University Department of Medicine
Cabrini Institute
154 Wattletree Rd
Malvern
Vic
3144
Country 68488 0
Australia
Phone 68488 0
+61 3 9508 3466
Fax 68488 0
Email 68488 0
[email protected]

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseTesting a new form to document 'Goals-of-Care' discussions regarding plans for end-of-life care for patients in an Australian emergency department.2018https://dx.doi.org/10.1111/1742-6723.12986
N.B. These documents automatically identified may not have been verified by the study sponsor.