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Palliative Care Referral System (PCRS) for Cancer Patients With Advanced Disease (PCRSS)

F

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano

Status

Completed

Conditions

Advanced Cancer

Treatments

Other: Palliative Care Referral System - PCRS

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Early palliative care (EPC) in the clinical pathway of advanced cancer patients improves symptom control, quality of life and has a positive impact on overall quality of care. EPC contributes to realistic and attainable goals of treatment, facilitating patient choices, favouring adequate communication with patients and families and assessing patient values and preferences with regard to advance care planning. EPC is likely to promote a more appropriate use of health care resources and less aggressive cancer treatment in the last weeks of life. At present standardised criteria for appropriate referral for EPC in oncology outpatients setting are lacking. Therefore the aim of this project is to identify referral criteria and procedures to implement appropriate EPC for advanced patients (the Palliative Care Referral System) and test them in a pre-post experimental design evaluating their impact on quality of care and on the use of healthcare resources. A quasi-experimental, longitudinal, pretest-posttest study will be carried out. Two different cohorts of 150 advanced cancer patients each will be enrolled before (pretest) and after (posttest) the introduction of the PCRS in outpatient clinics of a Comprehensive Cancer Centre. Eligible patients will undergo patient-reported outcome measure (PROMs) evaluation at baseline and then monthly for at least 6 months from enrollment or till death. Use health care resources and quality of care indicators will be collected monthly by a dedicated research nurse.

Full description

As above.

Enrollment

380 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age >18 years;
  • recent diagnosis of inoperable locally advanced and/or metastatic cancer not eligible to anticancer treatment with curative intent;

Exclusion criteria

  • cognitive impairment that would prevent self-assessments
  • current palliative care treatment

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

380 participants in 2 patient groups

control
No Intervention group
Description:
standard oncology care
intervention
Experimental group
Description:
standardized referral to outpatient palliative care by oncologists
Treatment:
Other: Palliative Care Referral System - PCRS

Trial contacts and locations

1

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Central trial contact

Augusto T Caraceni, MD

Data sourced from clinicaltrials.gov

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