Effectiveness of a specialist palliative home care nurse–patient consultation followed by an interprofessional telephone case conference compared with usual care among patients with non-oncological palliative care needs: protocol for the multicentre KOPAL cluster-randomised controlled trial
Judith Dams,
Hans-Helmut König,
Tim Friede,
Nils Schneider,
Stephanie Stiel,
Martin Scherer,
Silke Böttcher,
Gabriella Marx,
Ingmar Schäfer,
Nadine Janis Pohontsch,
Hendrik van den Bussche,
Friedemann Nauck,
Michael Freitag,
Eva Hummers,
Tina Mallon,
Franziska Schade,
Manuel Zimansky,
Thomas Asendorf,
Christiane A Mueller
Affiliations
Judith Dams
Hamburg Center for Health Economics, Hamburg, Germany
Hans-Helmut König
Department of Health Economics and Health Services Research, University Medical Center Hamburg-Eppendorf, Hamburg, Hamburg, Germany
Tim Friede
Department of Medical Statistics, University Medical Center Göttingen, Göttingen, Germany
Nils Schneider
Institute for General Practice and Palliative Care, Hannover Medical School, Hannover, Germany
Stephanie Stiel
Institute for General Practice and Palliative Care, Hannover Medical School, Hannover, Germany
Martin Scherer
Institute and Polyclinic for Primary Care and Family Medicine, University Medical Center Hamburg-Eppendorf (UKE), Hamburg, Germany
Silke Böttcher
Division of General Practice, Carl von Ossietzky University of Oldenburg, Oldenburg, Germany
Gabriella Marx
Department of General Practice and Primary Care, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Ingmar Schäfer
Department of Primary Medical Care, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Nadine Janis Pohontsch
Department of General Practice and Primary Care, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Hendrik van den Bussche
Department of General Practice and Primary Care, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Friedemann Nauck
Department of Palliative Medicine, University Medical Center Göttingen, Gottingen, Germany
Michael Freitag
Division of General Practice, Carl von Ossietzky University of Oldenburg, Oldenburg, Germany
Eva Hummers
1 Department of General Practice, University Medical Center Göttingen, Göttingen, Germany
Tina Mallon
Department of General Practice and Primary Care, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Franziska Schade
Department of Palliative Medicine, University Medical Center Göttingen, Gottingen, Germany
Manuel Zimansky
Institute for General Practice and Palliative Care, Hannover Medical School, Hannover, Germany
Thomas Asendorf
Department of Medical Statistics, University Medical Center Goettingen, Goettingen, Germany
Christiane A Mueller
Department of General Practice, University Medical Center Goettingen, Goettingen, Germany
Introduction Progressive chronic, non-malignant diseases (CNMD) like congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD) and dementia are of growing relevance in primary care. Most of these patients suffer from severe symptoms, reduced quality of life and increased numbers of hospitalisations. Outpatient palliative care can help to reduce hospitalisation rate by up to 50%. Due to the complex medical conditions and prognostic uncertainty of the course of CNMD, early interprofessional care planning among general practitioners who provide general palliative care and specialist palliative home care (SPHC) teams seems mandatory. The KOPAL study (a concept for strenghtening interprofessional collaboration for patients with palliative care needs) will test the effectiveness of a SPHC nurse–patient consultation followed by an interprofessional telephone case conference.Methods and analysis Multicentre two-arm cluster randomised controlled trial KOPAL with usual care as control arm. The study is located in Northern Germany and aims to recruit 616 patients in 56 GP practices (because of pandemic reasons reduced to 191 participants). Randomisation will take place on GP practice level immediately after inclusion (intervention group/control group). Allocation concealment is carried out on confirmation of participation. Patients diagnosed with CHF (New York Heart Association (NYHA) classification 3–4), COPD (Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage classification 3–4, group D) or dementia GDS stage 4 or above). Primary outcome is a reduced hospital admission within 48 weeks after baseline, secondary outcomes include symptom burden, quality of life and health costs. The primary analysis will follow the intention-to-treat principle. Intervention will be evaluated after the observation period using qualitative methods.Ethics and dissemination The responsible ethics committees of the cooperating centres approved the study. All steps of data collection, quality assurance and data analysis will continuously be monitored. The concept of KOPAL could serve as a blueprint for other regions and meet the challenges of geographical equity in end-of-life care.Trial registration number DRKS00017795; German Clinical Trials Register.