NCT03297320

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
400

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2017

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2017

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

September 26, 2017

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 29, 2017

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2018

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2019

Completed
Last Updated

September 29, 2017

Status Verified

September 1, 2017

Enrollment Period

2 years

First QC Date

September 26, 2017

Last Update Submit

September 26, 2017

Conditions

Keywords

Advance Care Planning, End of life, CPR

Outcome Measures

Primary Outcomes (1)

  • Incidence of Discordance

    Discordance between patients' prior expressed preferences and those documented in their healthcare record

    2 years

Secondary Outcomes (1)

  • Risk factors associated with discordance

    2 years

Study Arms (2)

Team Referrals

ACTIVE COMPARATOR

In-depth conversations about Goals of Care and ACP (the intervention) will be held for the patients referred to the research team by the three healthcare teams in Internal Medicine at London Health Sciences Centre (University Campus)

Other: In-depth conversation about Goals of Care and ACP

Random selection

ACTIVE COMPARATOR

A random selection of patients (not referred to the research team by the healthcare team) in Internal Medicine at London Health Sciences Centre (University Campus) will be selected to have in-depth conversations about Goals of Care and ACP (the intervention)

Other: In-depth conversation about Goals of Care and ACP

Interventions

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

Random selectionTeam Referrals

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients admitted to internal medicine teams at or after hospitalization day 2 with:
  • 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
  • If none of these criteria were met, any patient whose death within the next 1 year would not surprise health-care team members.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

London Health Sciences Centre

London, Ontario, N6A 5A5, Canada

RECRUITING

MeSH Terms

Conditions

Death

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Ravi Taneja, FRCPC

    Western University, Canada

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Launa Elliott, BSc

CONTACT

Ravi Taneja, FRCPC

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: 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
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 26, 2017

First Posted

September 29, 2017

Study Start

January 1, 2017

Primary Completion

December 31, 2018

Study Completion

March 31, 2019

Last Updated

September 29, 2017

Record last verified: 2017-09

Data Sharing

IPD Sharing
Will not share

Locations