PALLiON - PALLiative Care In ONcology

NCT ID: NCT03088202

Last Updated: 2023-03-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

659 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-03-22

Study Completion Date

2022-12-31

Brief Summary

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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

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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.

Conditions

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Neoplasia Prostate

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

No masking, the randomization applies to institutions, not patients

Study Groups

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Intervention arm

Educational program Standardized care pathways Early palliative care

Group Type EXPERIMENTAL

Educational program

Intervention Type OTHER

E-learning lectures, group exercises, skills training

Standardized care pathways

Intervention Type OTHER

Pathways for systematic follow-up

Early palliative care

Intervention Type OTHER

Compulsory referral to palliative care at inclusion

Control arm

Usual care

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Educational program

E-learning lectures, group exercises, skills training

Intervention Type OTHER

Standardized care pathways

Pathways for systematic follow-up

Intervention Type OTHER

Early palliative care

Compulsory referral to palliative care at inclusion

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Norwegian University of Science and Technology

OTHER

Sponsor Role collaborator

Oslo University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Marianne Jensen Hjermstad

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jon H Loge, PhD

Role: PRINCIPAL_INVESTIGATOR

Professor

Locations

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University Hospital of North Norway

Tromsø, Troms, Norway

Site Status

Ålesund Hospital Trust

Ålesund, , Norway

Site Status

Nordland Hospital Trust

Bodø, , Norway

Site Status

Østfold Hospital Trust

Fredrikstad, , Norway

Site Status

Førde Hospital Trust

Førde, , Norway

Site Status

Sørlandet Hospital Trust

Kristiansand, , Norway

Site Status

Akershus University Hospital

Oslo, , Norway

Site Status

Oslo University Hospital

Oslo, , Norway

Site Status

Telemark Hospital Trust

Skien, , Norway

Site Status

Stavanger University Hospital

Stavanger, , Norway

Site Status

Norwegian University of Science and Technology

Trondheim, , Norway

Site Status

Vestfold Hospital trust

Tønsberg, , Norway

Site Status

Countries

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Norway

References

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Hjermstad MJ, Pirnat A, Aass N, Andersen S, Astrup GL, Dajani O, Garresori H, Guldhav KV, Hamre H, Haukland EC, Jordal F, Lundeby T, Lohre ET, Mjaland S, Paulsen O, Semb KA, Staff ES, Wester T, Kaasa S. PALLiative care in ONcology (PALLiON): A cluster-randomised trial investigating the effect of palliative care on the use of anticancer treatment at the end of life. Palliat Med. 2024 Feb;38(2):229-239. doi: 10.1177/02692163231222391. Epub 2024 Jan 9.

Reference Type DERIVED
PMID: 38193250 (View on PubMed)

Lundeby T, Finset A, Kaasa S, Wester TE, Hjermstad MJ, Dajani O, Wist E, Aass N. A complex communication skills training program for physicians providing advanced cancer care - content development and barriers and solutions for implementation. J Commun Healthc. 2023 Mar;16(1):46-57. doi: 10.1080/17538068.2022.2039468. Epub 2022 Feb 20.

Reference Type DERIVED
PMID: 36919800 (View on PubMed)

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.

Reference Type DERIVED
PMID: 32241299 (View on PubMed)

Other Identifiers

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2016/1220REK

Identifier Type: -

Identifier Source: org_study_id

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