ArticleStigma and health2019
Experienced facial masking indirectly compromises quality of life through stigmatization of women and men with Parkinson's disease.
Article in Stigma and health, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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
11 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Exploring the stigma experienced by people affected by Parkinson's disease: a systematic review.BMC public health · 2025Pooled it
- The social cost of facial bradykinesia: a scoping review of interpersonal outcomes related to Parkinsonian hypomimia.Journal of neural transmission (Vienna, Austria : 1996) · 2026Review
- Stigma and social symptoms in Parkinson's disease: A scoping review.Clinical parkinsonism & related disorders · 2026Review
- Changes in Subjective Cognitive and Social Functioning in Parkinson's Disease from Before to During the COVID-19 Pandemic.Healthcare (Basel, Switzerland) · 2025Article
- The Story behind the Mask: A Narrative Review on Hypomimia in Parkinson's Disease.Brain sciences · 2024Review
- Validation Study of the Parkinson's Disease Stigma Questionnaire (PDStigmaQuest).Journal of Parkinson's disease · 2024Article
- Facial emotion expressivity in patients with Parkinson's and Alzheimer's disease.Journal of neural transmission (Vienna, Austria : 1996) · 2024Article
- Narrative medicine pinpoints loss of autonomy and stigma in Parkinson's disease.NPJ Parkinson's disease · 2023Article
- Parkinson's Disease Stigma Questionnaire (PDStigmaQuest): Development and Pilot Study of a Questionnaire for Stigma in Patients with Idiopathic Parkinson's Disease.Journal of Parkinson's disease · 2023Review
- Profile of social self-management practices in daily life with Parkinson's disease is associated with symptom severity and health quality of life.Disability and rehabilitation · 2021Article
- Social Symptoms of Parkinson's Disease.Parkinson's disease · 2020Review
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
This study examined the relationship between self-reported facial masking and quality of life (QoL) in people with Parkinson's disease (PD), and tested experienced stigma as a mediator and gender as a moderator of this relationship. The strength of stigma as a mediator was compared against an alternative mediator, depression. Ninety people with PD (34 women) rated difficulty showing facial expression (masking), and completed the Stigma Scale for Chronic Illness, Geriatric Depression Scale (15-item), and Parkinson's Disease Questionnaire-39. A conditional process model tested the indirect effect of facial masking on QoL through stigma, separately for women and men. A parallel indirect model included both stigma and depression to compare their statistical and clinical significance as mediators. Gender-moderated mediation of stigma reduced the association between facial masking and QoL to non-significance, suggesting stigma explained the association between facial masking and QoL. While facial masking was more stigmatizing for women than for men, stigma mediated the facial masking-QoL association for both women and men. Stigma (controlling for depression) reached a statistically and clinically significant level of mediation, whereas depression (controlling for stigma) reached a statistically yet not clinically significant level of mediation. People with PD who experience more severe facial masking feel more stigmatized, especially women. Regardless of gender, an increase in stigma from facial masking increases the likelihood of compromised QoL that reaches both statistical and clinical levels of significance.
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Registered trials
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