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PACE: cluster randomised controlled trial on ‘PACE Steps to Success' palliative care programme in Long Term Care Facilities in Europe

Comparative Effectiveness Research in long term care facilities in Europe - randomised controlled cluster trial on ‘PACE Steps to Success' palliative care programme

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14741671
Enrollment
80
Registered
2015-07-30
Start date
2015-06-01
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Older people living in long term care facilities Not Applicable

Interventions

In each country, six of 12 LTCFs will be randomized to the intervention group, in which they will receive the support of a Country Trainer and with the aid of a self-appointed PACE coordinator in the

Sponsors

European Commission
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: To enhance comparability between countries, LTCFs are eligible to be recruited when they fulfil all of the following inclusion criteria: 1. An off-site family physician or GP is responsible for the resident’s medical care. 2. Social and nursing care is provided onsite . 3. Number of beds per facility is at least 30 but does not exceed 100. 4. We strive to include facilities with at least 15 deceased residents in or outside the facility over the last year. If it is not possible to find enough LTCFs that fit this inclusion criterion, facilities should be selected in which the number of deceased residents in the past year is closest to 15. 5. LTCFs from a predefined geographical location (to be determined by the researchers). 6. Each partner lists all LTCFs fitting these inclusion criteria. From this list, only those LTCFs where the Board of Directors (1) expresses explicit motivation to participate in the study and (2) agrees to free time for one PACE coordinator for e.g. 0.5 days per working week, depending on setting, will be included in the study.

Exclusion criteria

Exclusion criteria: Researchers exclude facilities already using a palliative care planning tool e.g. (accredited users of) the Gold Standards Framework, Route to Success, Six Steps to Success, interRAI-PC version or end of life care integrated pathways such as Liverpool Care Pathway; or those facilities where they judge explicit and detailed palliative care guidelines to be available and corresponding high-quality practices to be implemented.

Design outcomes

Primary

MeasureTime frame
1. Quality of dying of the residents is measured using structured after-death questionnaires including validated instruments like EOLD-CAD (End-Of-Life in Dementia - Comfort Assessment in Dying) and QOD-LTC (Quality of Dying in Long-Term Care) at baseline, month 13 and month 17 after the start of the trial period 2. Staff knowledge and attitudes is measured using structured questionnaires including validated instrument like the ECPS (End-of-Life Professional Caregiver Survey), PCS (Palliative Care Survey) and S-EOLC (Self-Efficacy in End-of-Life Care Survey) at baseline and month 13 after the start of the trial period

Secondary

MeasureTime frame
Quality of palliative care is measured using structured after-death questionnaires including validated instruments like EOLD-SWC (End-Of-Life in Dementia - Satisfaction With Care) and FPPFC (Family Perception of Physician-Family Communication) at baseline, month 13 and month 17 after the start of the trial period.

Countries

Belgium, England, Finland, Italy, Netherlands, Poland, Switzerland, United Kingdom

Contacts

Public ContactYuliana Gatsolaeva
yuliana.gatsolaeva@vub.be+32 (0)2 477 49 43

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 7, 2026