Patients’ and caregivers’ perception of multidimensional and palliative care in amyotrophic lateral sclerosis – protocol of a German multicentre study
-
Published:2024-07-04
Issue:1
Volume:6
Page:
-
ISSN:2524-3489
-
Container-title:Neurological Research and Practice
-
language:en
-
Short-container-title:Neurol. Res. Pract.
Author:
Linse KatharinaORCID, Weber Constanze, Reilich Peter, Schöberl Florian, Boentert Matthias, Petri Susanne, Rödiger Annekathrin, Posa Andreas, Otto Markus, Wolf Joachim, Zeller Daniel, Brunkhorst Robert, Koch Jan, Hermann Andreas, Großkreutz Julian, Schröter Carsten, Groß Martin, Lingor Paul, Machetanz Gerrit, Semmler Luisa, Dorst Johannes, Lulé Dorothée, Ludolph Albert, Meyer Thomas, Maier André, Metelmann Moritz, Regensburger Martin, Winkler Jürgen, Schrank Berthold, Kohl Zacharias, Hagenacker Tim, Brakemeier Svenja, Weyen Ute, Weiler Markus, Lorenzl Stefan, Bublitz Sarah, Weydt Patrick, Grehl Torsten, Kotterba Sylvia, Lapp Hanna-Sophie, Freigang Maren, Vidovic Maximilian, Aust Elisa, Günther René
Abstract
Abstract
Introduction
Amyotrophic lateral sclerosis (ALS) is an inevitably fatal condition that leads to a progressive loss of physical functioning, which results in a high psychosocial burden and organizational challenges related to medical care. Multidimensional and multiprofessional care is advised to meet the complex needs of patients and their families. Many healthcare systems, including Germany, may not be able to meet these needs because non-medical services such as psychological support or social counselling are not regularly included in the care of patients with ALS (pwALS). Specialised neuropalliative care is not routinely implemented nor widely available. Caregivers of pwALS are also highly burdened, but there is still a lack of support services for them.
Methods
This project aims to assess the perceptions and satisfaction with ALS care in Germany in pwALS and their caregivers. This will be achieved by means of a cross-sectional, multicentre survey. The examination will assess, to which extend the patients’ needs in the six domains of physical, psychological, social, spiritual, practical and informational are being met by current care structures. This assessment will be linked to mental well-being, subjective quality of life, attitudes toward life-sustaining measures and physician-assisted suicide, and caregiver burden. The study aims to recruit 500 participants from nationwide ALS centres in order to draw comprehensive conclusions for Germany. A total of 29 centres, mostly acquired via the clinical and scientific German Network for Motor Neuron Diseases (MND-NET), will take part in the project, 25 of which have already started recruitment.
Perspective
It is intended to provide data-based starting points on how current practice of care in Germany is perceived pwALS and their caregivers and how it can be improved according to their needs. Planning and initiation of the study has been completed.
Trial registration
The study is registered at ClinicalTrails.gov; NCT06418646
Funder
Deutsche Gesellschaft für Muskelkranke ALS Association Universitätsklinikum Carl Gustav Carus Dresden an der Technischen Universität Dresden
Publisher
Springer Science and Business Media LLC
Reference25 articles.
1. Rosenbohm, A., Peter, R. S., Erhardt, S., Lulé, D., Rothenbacher, D., Ludolph, A. C., & Nagel, G. (2017). Epidemiology of amyotrophic lateral sclerosis in Southern Germany. J Neurol, 264(4), 749–757. 2. Chiò, A., Logroscino, G., Traynor, B. J., Collins, J., Simeone, J. C., Goldstein, L. A., & White, L. A. (2013). Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature. Neuroepidemiology, 41(2), 118–130. 3. Oh, J., & Kim, J. A. (2017). Supportive care needs of patients with amyotrophic lateral sclerosis/motor neuron disease and their caregivers: a scoping review. J Clin Nurs, 26(23–24), 4129–4152. 4. van Groenestijn, A. C., Kruitwagen-van Reenen, E. T., Visser-Meily, J. M., van den Berg, L. H., & Schröder, C. D. (2016). Associations between psychological factors and health-related quality of life and global quality of life in patients with ALS: a systematic review. Health Qual Life Outcomes, 14(1), 107. 5. Linse, K., Rüger, W., Joos, M., Schmitz-Peiffer, H., Storch, A., & Hermann, A. (2018). Usability of eyetracking computer systems and impact on psychological wellbeing in patients with advanced amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener, 19(3–4), 212–219.
|
|