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PROject - Supportive and Palliative Care and INnOvation - Antwerp (Pro-Spinoza)

Implementation of the Care Pathway for Primary Palliative Care in Five Research Clusters in Belgium

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02266069
Acronym
pro-Spinoza
Enrollment
24
Registered
2014-10-16
Start date
2014-10-31
Completion date
2016-12-31
Last updated
2017-11-29

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

Conditions

Palliative Care, Primary Health Care

Keywords

implementation, anticipatory care planning, symptom assessment, interdisciplinary collaboration

Brief summary

It is important to provide high quality palliative care to all patients with a non-curable and life-limiting condition. The Care Pathway for Primary Palliative Care (CPPPC) provides tools for health care professionals to help them delivering palliative care timely and accurately.This study investigates whether the implementation of the CPPPC really helps to improve patients' lifes.

Interventions

OTHERCare Pathway for Primary Palliative Care

Early identification of palliative care patients, anticipatory care planning, systematic symptom assessment, interdisciplinary collaboration, rigorous follow-up of the functional status of the patient and giving attention to the informal care givers.

Sponsors

Intermutualistic Agency
CollaboratorOTHER
National Institute for Health and Disability Insurance, Belgium
CollaboratorUNKNOWN
Bert Leysen
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* identified as a palliative care patient using the Surprise Question Would you, as a family doctor, be surprised if this patient would die in the next 12 months?. If the answer is 'no', the patient is eligible for the study.

Exclusion criteria

* not having signed the informed consent.

Design outcomes

Primary

MeasureTime frameDescription
percentage of deaths occurred in the hospital (of patients per family doctor/per research cluster)6 monthsThe hypothesis is that the CPPPC reduces the percentage of deaths occurred in the hospital

Secondary

MeasureTime frameDescription
cost of health care consumption in the last year of life (of patients per family doctor/per research cluster)6 monthsThe hypothesis is that the CPPPC reduces the cost of health care consumption in the last year of life
consumption of antibiotics in the last year of life (of patients per family doctor/per research cluster)6 monthsThe hypothesis is that the CPPPC reduces the consumption of antibiotics in the last year of life
consumption of pain killers in the last year of life (of patients per family doctor/per research cluster)6 monthsThe hypothesis is that the CPPPC augments the consumption of pain killers in the last year of life
consumption of (invasive) diagnostic and therapeutic procedures in the last year of life (of patients per family doctor/per research cluster)6 monthsThe hypothesis is that the CPPPC reduces the consumption of (invasive) diagnostic and therapeutic procedures in the last year of life

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026