ArticleParkinsonism & related disorders2019
Measuring quality of life in palliative care for Parkinson's disease: A clinimetric comparison.
Article in Parkinsonism & related disorders, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 4 of them syntheses that pooled it.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
15 citing papers in PubMed, 4 syntheses or guidelines pooled it.
- Cross-national disparities in end-of-life outcomes and care strategies for Parkinson's disease: a systematic review and meta-analysis of China and the United States.BMC health services research · 2026Pooled it
- Quality of life measures in Parkinson's disease: a systematic literature review of patient-reported outcomes measures (PROMs) and their psychometric properties.Journal of neurology · 2025Pooled it
- How best to capture the impact of complementary therapies in palliative care: A systematic review to identify and assess the appropriateness and validity of multi-domain tools.Palliative medicine · 2022Pooled it
- Palliative Care Intervention Trials for Adults Living With Progressive Central Nervous System Diseases and Their Caregivers: A Systematic Review.Journal of pain and symptom management · 2022Pooled it
- Outcomes of home-based primary care for homebound older adults: A randomized clinical trial.Journal of the American Geriatrics Society · 2023Trial
- Toward a Novel Phenotypic Classification of Parkinson's Disease for Rehabilitation: A Case Series.Cureus · 2026Article
- Far from being the end of the road: taking a closer look at neuropalliative care in Parkinson's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2025Review
- The Development of a Quantitative Disability Assessment Tool in Patients with Idiopathic Parkinson's Disease.Diagnostics (Basel, Switzerland) · 2024Article
- Economic Burden of Parkinson's Disease: A Multinational, Real-World, Cost-of-Illness Study.Drugs - real world outcomes · 2024Article
- Country-specific reference values for PROMISAnnals of medicine · 2023Article
- Common patient-reported outcomes across ICHOM Standard Sets: the potential contribution of PROMIS®.BMC medical informatics and decision making · 2021Article
- Associated Factors on Quality of Life in Patients with Parkinson's Disease.Brain & NeuroRehabilitation · 2021Article
- Palliative Care for Parkinson's Spectrum Disorders: an Emerging Approach.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020Review
- Interpretation of health-related quality of life outcomes in Parkinson's disease from the EARLYSTIM Study.PloS one · 2020Article
- Impact of disease stage and age at Parkinson's onset on patients' primary concerns: Insights for targeted management.PloS one · 2020Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
introductionQuality of life (QOL) assessments allow for more complete evaluation of patients' lived experiences in relation to chronic conditions, such as Parkinson's disease (PD). In palliative care, such instruments are vital to ensure QOL issues are catalogued and addressed for patients. However, little is known regarding the psychometric properties of quality of life scales for use in palliative care for PD, specifically.
methods210 participants with parkinsonian disorders, who participated in a larger palliative intervention clinical trial, completed four quality of life scales (PDQ-39, PROMIS-29, QOL-AD, and McGill QOL) at baseline and post-intervention. Psychometric properties, including internal consistency and concurrent validity, were examined. Factor analyses were performed to evaluate relationships between scale items. Minimal clinically important differences (MCID) and responsiveness were calculated for each scale.
resultsAll scales demonstrated good internal consistency and concurrent validity. Factor analyses revealed few deviations from the defined subdomains of the scales. Mean absolute MCID values were estimated at 12.7, 10.9, 3.9, and 18.9 for PDQ-39, PROMIS-29, QOL-AD, and McGill QOL, respectively. The PDQ-39 and PROMIS-29 demonstrated higher responsiveness to palliative intervention, while the QOL-AD was more responsive in the control group.
conclusionsThe PDQ-39, PROMIS-29, QOL-AD, and McGill QOL are all valid for use in PD palliative care, though subdomains of the scales in this population may differ slightly from those initially defined. We recommend the use of PDQ-39 and PROMIS-29 as outcome measures in clinical trials for palliative care in PD, though the QOL-AD may be superior for tracking disease progression.
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