Ireland
--:--IST
Enrolling by invitation Not applicable

Clinical Surveillance Tool to Screen for Unmet Palliative Needs Among Patients in the Final Year of Life

NCT04171830 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2019-06-17
Last updated
2026-07-20

Condition(s) studied

Palliative TherapyImplementation ScienceScreeningTerminal Care

Investigational drug(s) / intervention(s)

modified Hospital One-year Mortality Risk (mHOMR)

modified Hospital One-year Mortality Risk (mHOMR): Every inpatient will automatically be given the intervention (an mHOMR/HOMR Now! score) upon admission to hospital and considered for secondary interventions based on their score. Baseline threshold will be set as \>0.21 (59% sensitivity and 90% specificity for 12-month mortality with mHOMR). At minimum each individual identified by the tool will receive two assessments to screen for severe symptoms and desire to engage in advance care planning (ACP): 1. Edmonton Symptom Assessment System Revised: scores \>6 will be flagged as severe. Clinical teams will address the symptoms as appropriate for the patient. 2. 4-item Advanced Care Planning Engagement Survey: Scores of 3-4 indicate readiness to discuss ACP. Clinical teams may choose to discuss ACP and goals of care themselves, activate a local ACP intervention, or distribute ACP documentation. Both of these assessments will be done by a member of the treating team within 72 hours of the patient's hospital admission.

Study summary

One of the most important obstacles to improving end-of-life care is the inability of clinicians to reliably identify those who are approaching the end-of-life. Every aspect of a palliative approach to care - screening for unmet needs, treating symptoms, discussing goals of care, and developing a palliative management plan - depends on the reliable and accurate identification of patients with palliative needs. The investigators developed an accurate and reliable mortality prediction tool that automatically identifies patients in hospital at elevated risk of death in the coming year. In previous studies it has been shown that these patients also frequently have unmet palliative care needs at the time they are identified by the tool. This tool has been demonstrated feasible, acceptable to patients and providers, and effective for changing physician behaviour in an inpatient clinical context.

In this project, this tool is implemented as part of an integrated knowledge translation project to facilitate reliable and timely identification of unmet palliative needs across multiple hospitals with different clinical settings and contexts. The investigators have partnered with 12 hospitals to improve the quality of palliative and end-of-life care provided to patients and families. With each partner site the investigators will develop a comprehensive implementation plan, including stakeholder engagement, education, and feedback. Process measures will be collected at each site to determine whether the tool was effective for promoting the identification and documentation of unmet palliative needs. Patients who were identified by the tool will also be followed over time to collect outcome and impact measures to see if their end-of-life care was affected by the intervention compared to control groups.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * All newly admitted patients to selected medical units in participating sites during the 6-9-month intervention implementation period * \[To be assessed for unmet palliative needs\] the patient must be competent and have the ability to participate in assessments (i.e. answer assessment questions and understand and speak sufficient English to participate). Exclusion Criteria: * N/A for mHOMR/HOMR-Now! intervention * For palliative needs assessments: incapability of completing the ESAS and 4-Item ACP tools, either because of capacity/cognitive impairment or English-language ability.

Primary outcome measure(s)

  • Identification and documentation of unmet palliative needs — Through study completion, up to 9 months
    Proportion of admissions at each site identified by the application
  • Identification and documentation of unmet palliative needs — Through study completion, up to 9 months
    Proportion of admissions with a HOMR (modified or Now!) score \>0.21 with ESAS symptom score \>6 and/or documented desire to engage in ACP via the 4-item ACP Engagement Survey

Trial sites (13)

FacilityCityRegionStatus
William Osler Health System Brampton Ontario
Cambridge Memorial Hospital Cambridge Ontario
Kingston Health Sciences Centre Kingston Ontario
London Health Sciences Centre London Ontario
Headwaters Health Care Centre Orangeville Ontario
The Ottawa Hospital Ottawa Ontario
Montfort Hospital Ottawa Ontario
Queensway Carleton Hospital Ottawa Ontario
Pembroke Regional Hospital Pembroke Ontario
North York General Hospital Toronto Ontario
Humber River Hospital Toronto Ontario
Saint Michael's Hospital Toronto Ontario
Windsor Regional Hospital Windsor Ontario
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04171830 on ClinicalTrials.gov ↗ ← All trials in Canada