Partnering with general practitioners to optimize survivorship for patients with lymphoma: a phase II randomized controlled trial (the GOSPEL I trial).


Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
06 Jan 2021
Historique:
received: 17 06 2020
accepted: 01 12 2020
entrez: 7 1 2021
pubmed: 8 1 2021
medline: 22 6 2021
Statut: epublish

Résumé

Survival rates for lymphoma are highest amongst hematological malignancies. In 2019, it was estimated that over 6400 Australians were diagnosed with lymphoma, a group of hematological malignancies with a high 5-year survival rate of ~ 76%. There is an increased focus on the promotion of wellness in survivorship and active approaches to reducing morbidity related to treatment; however, current models of follow-up care heavily rely on hospital-based specialist-led care. Maximizing the potential of general practitioners (GPs) in the ongoing management of cancer is consistent with the national health reform principles and the Cancer Council Australia's Optimal Care Pathways. GPs are well positioned to provide guideline-based follow-up care and are more likely to address comorbidities and psychosocial issues and promote healthy lifestyle behaviors. This study aims to test the feasibility of the GOSPEL I intervention for implementing an integrated, shared care model in which cancer center specialists and community-based GPs collaborate to provide survivorship care for patients with lymphoma. We describe a protocol for a phase II, randomized controlled trial with two parallel arms and a 1:1 allocation. Sixty patients with Hodgkin's and non-Hodgkin's lymphoma will be randomized to usual specialist-led follow-up care (as determined by the treating hematologists) or a shared follow-up care intervention (i.e., GOSPEL I). GOSPEL I is a nurse-enabled, pre-specified shared care pathway with follow-up responsibilities shared between cancer center specialists (i.e., hematologists and specialist cancer nurses) and GPs. Outcome measures assess feasibility as well as a range of patient-reported outcomes including health-related quality of life as measured by the Functional Assessment of Cancer Therapy-Lymphoma, patient experience of care, symptom distress, comorbidity burden, dietary intake, physical activity behaviors, financial distress/interference, and satisfaction of care. Safety indicators including hospital admission and unscheduled lymphoma clinic visits as well as process outcomes such as intervention fidelity and economic indicators will be analyzed. This trial is designed to explore the feasibility and acceptability of a new model of shared care for lymphoma survivors. Patient-reported outcomes as well as potential barriers to implementation will be analyzed to inform a larger definitive clinical trial testing the effects and implementation of a shared care model on health-related quality of life of lymphoma survivors. Australia and New Zealand Clinical Trials Registry ACTRN12620000594921 . Registered on 22 May 2020.

Sections du résumé

BACKGROUND BACKGROUND
Survival rates for lymphoma are highest amongst hematological malignancies. In 2019, it was estimated that over 6400 Australians were diagnosed with lymphoma, a group of hematological malignancies with a high 5-year survival rate of ~ 76%. There is an increased focus on the promotion of wellness in survivorship and active approaches to reducing morbidity related to treatment; however, current models of follow-up care heavily rely on hospital-based specialist-led care. Maximizing the potential of general practitioners (GPs) in the ongoing management of cancer is consistent with the national health reform principles and the Cancer Council Australia's Optimal Care Pathways. GPs are well positioned to provide guideline-based follow-up care and are more likely to address comorbidities and psychosocial issues and promote healthy lifestyle behaviors. This study aims to test the feasibility of the GOSPEL I intervention for implementing an integrated, shared care model in which cancer center specialists and community-based GPs collaborate to provide survivorship care for patients with lymphoma.
METHODS METHODS
We describe a protocol for a phase II, randomized controlled trial with two parallel arms and a 1:1 allocation. Sixty patients with Hodgkin's and non-Hodgkin's lymphoma will be randomized to usual specialist-led follow-up care (as determined by the treating hematologists) or a shared follow-up care intervention (i.e., GOSPEL I). GOSPEL I is a nurse-enabled, pre-specified shared care pathway with follow-up responsibilities shared between cancer center specialists (i.e., hematologists and specialist cancer nurses) and GPs. Outcome measures assess feasibility as well as a range of patient-reported outcomes including health-related quality of life as measured by the Functional Assessment of Cancer Therapy-Lymphoma, patient experience of care, symptom distress, comorbidity burden, dietary intake, physical activity behaviors, financial distress/interference, and satisfaction of care. Safety indicators including hospital admission and unscheduled lymphoma clinic visits as well as process outcomes such as intervention fidelity and economic indicators will be analyzed.
DISCUSSION CONCLUSIONS
This trial is designed to explore the feasibility and acceptability of a new model of shared care for lymphoma survivors. Patient-reported outcomes as well as potential barriers to implementation will be analyzed to inform a larger definitive clinical trial testing the effects and implementation of a shared care model on health-related quality of life of lymphoma survivors.
TRIAL REGISTRATION BACKGROUND
Australia and New Zealand Clinical Trials Registry ACTRN12620000594921 . Registered on 22 May 2020.

Identifiants

pubmed: 33407797
doi: 10.1186/s13063-020-04945-4
pii: 10.1186/s13063-020-04945-4
pmc: PMC7787240
doi:

Types de publication

Clinical Trial, Phase II Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

12

Subventions

Organisme : Health Innovation, Investment and Research Office
ID : N/A

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Auteurs

Raymond Javan Chan (RJ)

Princess Alexandra Hospital and Queensland University of Technology (QUT), Brisbane, Queensland, Australia. Raymond.Chan@qut.edu.au.

Stephanie Buhagiar (S)

Division of Cancer Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Laisa Teleni (L)

Princess Alexandra Hospital and Queensland University of Technology (QUT), Brisbane, Queensland, Australia.

Camilla Simonsen (C)

Division of Cancer Services, Princess Alexandra Hospital and Queensland University of Technology (QUT), Brisbane, Queensland, Australia.

Jane Turner (J)

Faculty of Medicine, University of Queensland and Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.

Courtney Rawson (C)

Division of Cancer Services, Princess Alexandra Hospital and Queensland University of Technology (QUT), Brisbane, Queensland, Australia.

Nicolas H Hart (NH)

Cancer and Palliative Care Outcomes Centre, Queensland University of Technology (QUT), Brisbane, Queensland, Australia.

Lee Jones (L)

Princess Alexandra Hospital and Queensland University of Technology (QUT), Brisbane, Queensland, Australia.

Louisa Gordon (L)

QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

Ria Joseph (R)

Cancer and Palliative Care Outcomes Centre, Queensland University of Technology (QUT), Brisbane, QLD, Australia.

Oluwaseyifunmi Andi Agbejule (OA)

Princess Alexandra Hospital and Queensland University of Technology (QUT), Brisbane, Queensland, Australia.

Fiona Henderson (F)

Division of Cancer Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Joel Rhee (J)

University of Wollongong, Wollongong, Australia.

Marissa Ryan (M)

Division of Cancer Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Christine Carrington (C)

Division of Cancer Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Sally Mapp (S)

Division of Cancer Services, Princess Alexandra Hospital and Queensland University of Technology (QUT), Brisbane, Queensland, Australia.

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Classifications MeSH