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The Values and Preferences of People Living With Motor Neurone Disease (MND): A Systematic Review Protocol
Timothy Hugh Barker1, Grace Holland1, Camille Schubert2
1Health Evidence Synthesis, Recommendations and Impact (HESRI), School of Public Health, Faculty of Health and Medical Sciences The University of Adelaide Adelaide Australia.
Objective:
To systematically review the values and preferences of people with lived experience of motor neurone disease (MND), including those living with MND, caregivers and genetic carriers, regarding their health-related outcomes.
Introduction:
MND is a devastating neurodegenerative disease that significantly impacts those living with the disease, their caregivers, and their families. Understanding the values and preferences of those affected by MND is crucial for providing patient-centred care and developing trustworthy guidelines.
Eligibility Criteria:
Studies will be included if they report on the values and preferences of adults living with MND; caregivers and families of those diagnosed with MND; clinicians as a proxy for adults living with MND; or asymptomatic genetic carriers of MND. Peer-reviewed studies utilising either quantitative or qualitative methodologies (or both) will be eligible for inclusion in this review.
Methods And Analysis:
A comprehensive search of electronic databases will be conducted to identify relevant studies. Data extraction, risk of bias assessment (of quantitative studies), and assessment of methodological limitations (of qualitative studies) will be performed independently by two reviewers. Quantitative data will be pooled using meta-analysis where appropriate, and qualitative data will be synthesised following a modified meta-aggregative approach. The relevant GRADE approach will be used to assess the certainty of evidence.
Systematic Review Registration Number:
CRD420250653287.
