Frail Elderly Syndrome
Conditions
Keywords
Palliative care, End of life care, Long-term care, Nursing home
Brief summary
This study will evaluate the implementation of the Strengthening a Palliative Approach in Long-Term Care (SPA-LTC) program using a cross-jurisdictional, effectiveness-implementation type II hybrid design (dual testing of clinical and implementation interventions) to assess the implementation (feasibility, fidelity, reach, sustainability) and effectiveness (family satisfaction, staff knowledge and confidence implementing a palliative approach to care, hospital use).
Detailed description
The SPA-LTC program has been developed and refined through prior participatory action based studies. Evidence-based components of the program include: Palliative Champion Teams; Palliative Care Education, including illness-trajectory pamphlets for staff and family members; Comfort Care Rounds with staff; Prognostic Tools to trigger end-of-life discussions; Palliative Care Conferences; Bereavement Pamphlets for families; and Post-Bereavement Follow-Up for families, and staff The goal is to implement and assess this program across three provinces in Canada (Ontario, Saskatchewan, Manitoba). The investigators will use the findings to revise the program and inform the scaling up of the program across diverse settings and provinces.
Interventions
Our team will work with long-term care homes in the study to implement the Strengthening a Palliative Approach in Long Term Care (SPA-LTC) which consists of the following core, evidence-informed components: Palliative Champion Teams (to provide leadership and support implementation); Palliative Care Education (including illness trajectory pamphlets); Comfort Care Rounds with staff (for capacity building and reflection); Prognostic Tools to trigger end-of-life discussions; Palliative Care Conferences with families and residents; Bereavement Pamphlets; and Post-Bereavement Follow-Up for families, and staff.
Sponsors
Study design
Masking description
There is no need to mask participants, clinicians or research staff.
Intervention model description
Within each of the three provinces, six LTC homes will be randomly selected, and then randomly allocated using a 1:1 ratio, stratified according to province, to either the intervention or control group using a computer-generated list. For each province, three LTC homes will receive the intervention and three will receive usual care. A biostatistician not involved in recruitment will generate group assignments.
Eligibility
Inclusion criteria
* English-speaking LTC residents with a score of 50% or less on the Palliative Performance Scale.
Exclusion criteria
* Non-English speaking LTC residents * residents with a score of more than 50% on the Palliative Performance Scale.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of Emergency Department Visits in the Resident's Last Year of Life | All residents in the home who died one year prior to the implementation and one year prior to the date of death for all residents in the home who die during the study intervention period. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Family Perceptions of End of Life Care | Survey completed at enrolment into the study; survey completed 2 months after the Family Care Conference or 1 month after the end of the intervention period if no Family Care Conference occurred. | Survey |
| Family Experiences with End of Life Care | Interview completed at enrolment into the study; survey completed 2 months after the Family Care Conference or 1 month after the end of the intervention period if no Family Care Conference occurred. | Interview |
| Staff Knowledge about a Palliative Approach to Care | All staff in all participating long-term care homes will complete a staff survey at 2 points in the study: at the beginning and the end of the intervention | Survey |
| Number of Hospital Deaths during the trial | Chart audit at start of the trial to capture data on residents who died in the year prior to the trial. Chart audits also during the transition phase prior to Steps 2 and 3; and one month after the intervention period for the trial ends. | Chart data at each study site will be audited to capture data on the number of hospital deaths in the year prior to the trial and during the trial. Chart data at each study site will be audited to capture data on the number of hospital transfers in the residents last year of life. |
| Bereaved Family Satisfaction with End of Life Care | 6 weeks to 2 months after the resident's death | Qualitative interview with family members whose loved one died during the trial. |
| Resident Satisfaction with End of Life Care | At the time of enrolment and 2 months after the Family Care Conference or 1 month after the intervention period if no Family Care Conference occurred. | Qualitative interview with residents who are enrolled in the trial |
| Number of Hospital Transfers per Resident | Chart audit at start of the trial to capture data on residents who died in the year prior to the trial. Chart audits also during the transition phase prior to Steps 2 and 3; and one month after the intervention period for the trial ends. | Chart data at each study site will be audited to capture data on the number of hospital transfers in the last year of life for residents who died 1 year before the trial or who die during the trial. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Fidelity of the Intervention | Checklist completed weekly during the intervention period for up to 160 weeks. | Checklist |
Countries
Canada