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PALLiON - PALLiative Care In ONcology (PALLiON)

Primary Purpose

Neoplasia Prostate

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Educational program
Standardized care pathways
Early palliative care
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Neoplasia Prostate focused on measuring cancer, palliative care, PROMs, survival, QoL, referral

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • A verified metastatic or locally advanced cancer of the upper GI tract, lower GI tract, pancreas, liver, breast, bladder, prostate, kidney, cholangiocarcinoma, or malignant melanoma
  • Defined as a palliative care patient, with expected life expectancy of <12 months
  • Scheduled to start what is perceived as last line of chemotherapy (definition: tumor directed medical therapy)

    o Observe: different time points for inclusion and line of treatment apply for the specific diagnoses

  • Age > 18 years
  • Fluency in written and oral Norwegian
  • Physically and cognitively able to provide written informed consent, based on clinical judgment
  • Scheduled to receive all oncological and specialized palliative treatment at the participating hospital
  • World Health Organization (WHO) performance status 0-2

Exclusion Criteria:

  • Any serious psychiatric diagnosis (e.g. psychotic, bipolar disorder), substance abuse or cognitive impairment as judged by standard clinical criteria (disturbed consciousness, disorientation to time/place and attention deficits) at the discretion of the attending physician that precludes completion of PROs
  • A cancer diagnosis other than the ones above
  • Multiple malignancies
  • Serious substance abuse
  • Already included in a palliative care program

Sites / Locations

  • University Hospital of North Norway
  • Nordland Hospital Trust
  • Østfold Hospital Trust
  • Førde Hospital Trust
  • Sørlandet Hospital Trust
  • Akershus University Hospital
  • Oslo University Hospital
  • Telemark Hospital Trust
  • Stavanger University Hospital
  • Norwegian University of Science and Technology
  • Vestfold Hospital trust
  • Ålesund Hospital Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention arm

Control arm

Arm Description

Educational program Standardized care pathways Early palliative care

Usual care

Outcomes

Primary Outcome Measures

Use of chemotherapy
Number of patients who receive chemotherapy during their last 3 months of life

Secondary Outcome Measures

Initiation and discontinuation of chemotherapy
Number of patients who start and discontinue chemo, and number of cycles
Use of artificial nutrition
Number of patients who receive artificial nutrition during their last month of life
Use of concomitant medication
Number of patients who receive concomitant medication during their last month of life

Full Information

First Posted
January 30, 2017
Last Updated
March 23, 2023
Sponsor
Oslo University Hospital
Collaborators
Norwegian University of Science and Technology
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1. Study Identification

Unique Protocol Identification Number
NCT03088202
Brief Title
PALLiON - PALLiative Care In ONcology
Acronym
PALLiON
Official Title
PALLiON - PALLiative Care In ONcology - a Cluster-randomized Trial to Improve the Care for Cancer Patients With a Short Life Expectancy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
March 22, 2017 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
December 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
Norwegian University of Science and Technology

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A major concern in today's oncology is the complexity of treatment that increases costs. A main contributor is the increasing use of chemo- and radiotherapy during end of life (EoL: the last 12 months of life). Importantly, intensive chemotherapy in EoL has uncertain efficacy, may result in frequent hospitalizations and less time spent at home. Also, patients with incurable disease who receive intensive treatment at EoL have worse quality of life (QoL). A systematic palliative care (PC) approach that focuses on optimal symptom management and maintenance of QoL of patients and family is often introduced too late in the disease trajectory. Studies indicate that early introduction of PC in patients with unfavorable prognosis may improve QoL and other symptoms and prolong survival. These and related findings have made international stakeholders advocate a stronger integration of oncology and PC for patients with incurable cancer. The present project is a national multicenter cluster-randomized trial (RCT) in 12 oncology departments in all 4 Norwegian health regions. The project tests the efficacy of a complex tripod intervention that integrates oncology and PC for cancer patients with a life-expectancy <12 months who receive chemotherapy and includes: A) systematic electronic assessment of symptoms, B) implementation of standardized care pathways and C) an education program for oncologists/PC physicians. The PC pathway focuses on the patient's journey through the PC trajectory including EoL care in order to improve quality of care and reduce the variability in clinical practice and costs. The intervention aims at empowering physicians, patients and relatives and promoting shared-decision-making.
Detailed Description
Patients with incurable disease who receive intensive treatment at EoL have worse quality of life (QoL) compared with those receiving symptomatic treatment. Also, a PC approach at an early stage in patients with unfavorable prognosis may improve patients' QoL and symptom control, may lead to prolonged survival and give patients and caregivers a more realistic perspective on the disease and prognosis. Further, there is documentation that caregivers of patients with advanced cancer are generally more satisfied and report less depressive symptoms with an early introduction of PC. These and related findings in the wake of a study (NEJM 2010) initiated the current debate and have made international stakeholders advocate a stronger integration of oncology and PC for patients with incurable cancer. Despite a rapid development of PC services during the last 15-20 years, there is still a distinct separation between oncology and PC in Norway as in other Western countries. This infers that the potential for optimal care during the last phase of life for those patients has not been fully explored, despite the documented advantages for both patients and caregivers. However, results from studies on integration of oncology and PC from other countries e.g. the USA, may not be directly transferable to Norway, given the different health care organizations, reimbursement issues and the different indications for and the high degree of hospice use. Information given to cancer patients and caregivers about the disease and its treatment is important at all stages of disease, and is crucial in relation to PC in order to facilitate shared decision making, and improve satisfaction with care, patients' sense of control, QoL and communication with patient and caregivers. As PC also aims to improve the QoL of caregivers waiting to include caregivers until patients are in their last weeks or days of life may not adequately address patient or caregiver distress. Further, the benefits of early integration of PC on caregiver's distress and QoL remain inconclusive. Thus, the overall aim of PALLiON is to improve the quality and efficacy of cancer care by implementing an early integration of oncology and PC in patients with advanced cancer who receive chemotherapy. The long-term objective is a change of today's oncology practice. Today, the method of referral to PC is most often based on care needs in contrast to referrals based on diagnosis and prognosis used in the RCTs that have documented favorable results. As we know that the timing of referral is important to optimize the benefits of PC, we aim to change this practice. The implementation method in PALLiON is a complex intervention consisting of a) a structured educational program for oncologists, palliative care physicians and nurses, b) standardized care pathways with a systematic integration of oncology and palliative care for each of the included cancer diagnoses, and c) systematic use of Eir - an electronic assessment tool for patient-reported outcomes (PROMs), in the standardized care pathways, combined with evidence-based treatment recommendations in the clinical consultations. The design makes it possible to evaluate the effect of an early integration of oncology and PC at the institutional and patient levels between the intervention and control arms. Further, a potential effect of the intervention at each of the centers in the intervention arm can be evaluated by comparing the post-intervention data with historical data e.g. on use of chemotherapy, number of re-admissions / emergency admissions in the very last stages of life as appropriate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neoplasia Prostate
Keywords
cancer, palliative care, PROMs, survival, QoL, referral

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
No masking, the randomization applies to institutions, not patients
Allocation
Randomized
Enrollment
659 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention arm
Arm Type
Experimental
Arm Description
Educational program Standardized care pathways Early palliative care
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Usual care
Intervention Type
Other
Intervention Name(s)
Educational program
Intervention Description
E-learning lectures, group exercises, skills training
Intervention Type
Other
Intervention Name(s)
Standardized care pathways
Intervention Description
Pathways for systematic follow-up
Intervention Type
Other
Intervention Name(s)
Early palliative care
Intervention Description
Compulsory referral to palliative care at inclusion
Primary Outcome Measure Information:
Title
Use of chemotherapy
Description
Number of patients who receive chemotherapy during their last 3 months of life
Time Frame
3 months before death
Secondary Outcome Measure Information:
Title
Initiation and discontinuation of chemotherapy
Description
Number of patients who start and discontinue chemo, and number of cycles
Time Frame
3 months before death
Title
Use of artificial nutrition
Description
Number of patients who receive artificial nutrition during their last month of life
Time Frame
1 month before death
Title
Use of concomitant medication
Description
Number of patients who receive concomitant medication during their last month of life
Time Frame
1 month before death

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A verified metastatic or locally advanced cancer of the upper GI tract, lower GI tract, pancreas, liver, breast, bladder, prostate, kidney, cholangiocarcinoma, or malignant melanoma Defined as a palliative care patient, with expected life expectancy of <12 months Scheduled to start what is perceived as last line of chemotherapy (definition: tumor directed medical therapy) o Observe: different time points for inclusion and line of treatment apply for the specific diagnoses Age > 18 years Fluency in written and oral Norwegian Physically and cognitively able to provide written informed consent, based on clinical judgment Scheduled to receive all oncological and specialized palliative treatment at the participating hospital World Health Organization (WHO) performance status 0-2 Exclusion Criteria: Any serious psychiatric diagnosis (e.g. psychotic, bipolar disorder), substance abuse or cognitive impairment as judged by standard clinical criteria (disturbed consciousness, disorientation to time/place and attention deficits) at the discretion of the attending physician that precludes completion of PROs A cancer diagnosis other than the ones above Multiple malignancies Serious substance abuse Already included in a palliative care program
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jon H Loge, PhD
Organizational Affiliation
Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of North Norway
City
Tromsø
State/Province
Troms
ZIP/Postal Code
9019
Country
Norway
Facility Name
Nordland Hospital Trust
City
Bodø
Country
Norway
Facility Name
Østfold Hospital Trust
City
Fredrikstad
ZIP/Postal Code
1714
Country
Norway
Facility Name
Førde Hospital Trust
City
Førde
Country
Norway
Facility Name
Sørlandet Hospital Trust
City
Kristiansand
Country
Norway
Facility Name
Akershus University Hospital
City
Oslo
Country
Norway
Facility Name
Oslo University Hospital
City
Oslo
Country
Norway
Facility Name
Telemark Hospital Trust
City
Skien
Country
Norway
Facility Name
Stavanger University Hospital
City
Stavanger
Country
Norway
Facility Name
Norwegian University of Science and Technology
City
Trondheim
ZIP/Postal Code
0730
Country
Norway
Facility Name
Vestfold Hospital trust
City
Tønsberg
Country
Norway
Facility Name
Ålesund Hospital Trust
City
Ålesund
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
If desired, other collaborators may use data collected at their own institution. However, this is subject to approval from the study scientific committee, and only applies after publication of the main study publication
IPD Sharing Time Frame
end 2019
IPD Sharing Access Criteria
co-authorship use of own data for quality assurance / publications
Citations:
PubMed Identifier
32241299
Citation
Hjermstad MJ, Aass N, Andersen S, Brunelli C, Dajani O, Garresori H, Hamre H, Haukland EC, Holmberg M, Jordal F, Krogstad H, Lundeby T, Lohre ET, Mjaland S, Nordbo A, Paulsen O, Schistad Staff E, Wester T, Kaasa S, Loge JH. PALLiON - PALLiative care Integrated in ONcology: study protocol for a Norwegian national cluster-randomized control trial with a complex intervention of early integration of palliative care. Trials. 2020 Apr 2;21(1):303. doi: 10.1186/s13063-020-4224-4.
Results Reference
derived

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PALLiON - PALLiative Care In ONcology

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