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Advance Care Planning at London Health Sciences Centre

Advance Care Planning at London Health Sciences Centre

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03297320
Acronym
ACP@LHSC
Enrollment
400
Registered
2017-09-29
Start date
2017-01-01
Completion date
2019-03-31
Last updated
2017-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advance Care Planning

Keywords

Advance Care Planning, End of life, CPR

Brief summary

All patients admitted to London Health Sciences Centre (LHSC) are asked to indicate their preferences for CPR (cardiopulmonary resuscitation) and other life-sustaining treatments that necessitate an Intensive Care Unit (ICU) admission. Complex, high-risk patients at LHSC require multiple admissions to the hospital towards their end-of-life (EOL). Documentation of their resuscitation status should be a part of a broader dialogue with patients around their goals of care (GOC) and advance care planning (ACP), but rarely is this the case. The innovation will involve the use of trained nurse facilitators to have meaningful conversations with patients and their families in an effective way that bridges the gap between resuscitation status, GOC discussions and ACP across the continuum of care.

Detailed description

1. On admission, the usual LHSC process will be followed whereby the patient's wishes for resuscitation are documented on the resuscitation record in the patient's chart. This constitutes the original resuscitation status. 2. After referral or screening and written consent, the RA will conduct semi-structured, face-to-face interviews with the patient and or SDM as appropriate. If the RA has concern about a discordance, he/she will then provide verbal feedback to the health-care team (Attending Physician or the Senior Medical Resident (SMR)) immediately and request them to communicate with the patient/SDM again. A case of discordance shall be recorded ONLY if the health-care team (Attending Physician or Senior Medical Resident) confirms that a change in resuscitation status is needed. The output of this intervention will be the revised resuscitation status. This standardized process for determining this outcome has worked well in our pilot study. Any disagreements between RA and SMR on patient/SDM preferences will be reported to Team#1 Attending and recorded. It will be up to the team to reconcile the revised resuscitation preferences on official records (Resuscitation status can only be filled in only by an MD as per hospital policy). 4\. Advanced Clinical Notes: These will be typed by the RA and a note be made of the revised resuscitation preferences along with GOC and ACP discussions. 5\. A pilot study related to this work started in August 2016 and has allowed the research team to evaluate barriers and facilitators of conducting this intervention on Internal Medicine patients.

Interventions

OTHERIn-depth conversation about Goals of Care and ACP

In-depth conversation regarding Goals of Care and ACP by an experienced practitioner

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Healthcare teams in Internal Medicine at London Health Sciences Centre will be asked if they have any patients that need further goals of care discussions or ACP. A random selection of Internal Medicine patients will also be selected for further indepth conversations related to goals of care discussions or ACP

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients admitted to internal medicine teams at or after hospitalization day 2 with: 1. Age ≥55 years with ≥1 diagnoses: Chronic lung disease, Coronary artery disease, Congestive heart failure, Cirrhosis, Renal failure, Diabetes, Peripheral vascular disease, Cancer, Dementia (inability with ADLs) or 2. If none of these criteria were met, any patient whose death within the next 1 year would not surprise health-care team members.

Exclusion criteria

1. Lack of written consent 2. Patients who do not speak English; hard of hearing 3. Expected to die or be discharged ≤ 24 hours 4. Referral to or having an established palliative care plan

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Discordance2 yearsDiscordance between patients' prior expressed preferences and those documented in their healthcare record

Secondary

MeasureTime frameDescription
Risk factors associated with discordance2 yearsEvaluate predisposing factors for the discordance

Countries

Canada

Contacts

Primary ContactLauna Elliott, BSc
Ravi.Taneja@lhsc.on.ca519 685-8500
Backup ContactRavi Taneja, FRCPC
Ravi.Taneja@lhsc.on.ca519 685-8500

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026