“罕见的真实面孔”:罕见疾病患者及其社区对特定疾病材料中真实图像的偏好

Rare Pub Date : 2025-01-01 DOI:10.1016/j.rare.2025.100070
Laura Smith van Carroll , Pavel Krepelka , Kirsty Hoyle , Kamran Iqbal , Tom Kenny
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引用次数: 0

摘要

本研究探讨了罕见疾病患者及其社区在疾病特异性材料中使用真实图像的偏好。通过对50名受访者的数字调查,我们研究了在教育和宣传材料中使用受罕见疾病影响的人的图像的重要性。结果显示,人们对真实图像有强烈的偏好,大多数受访者认为这一点非常重要。罕见病患者表示,看到罕见病患者的“真实面孔”可以培养一种联系感,消除孤立感,并通过更多的接触提高公众意识。相反,一些受访者指出了基于外表的刻板印象的风险,这表明需要敏感、准确的描绘。我们的研究结果表明,对于那些患有罕见疾病的人及其社区来说,真实的图像可以提高参与度,并与材料建立情感联系。此外,我们还为这些材料的开发人员提供可操作的建议,包括患者倡导团体、研究机构和制药公司。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
“True Faces of Rare”: Preferences for authentic imagery in disorder-specific materials by people living with rare diseases and their communities
This study explores the preferences of people living with rare diseases and their communities regarding the use of authentic imagery in disorder-specific materials. Through a digital survey of 50 respondents, we examined the perceived importance of using images of people affected by a rare disorder in educational and awareness materials about their specific disorder. Results reveal a strong preference for authentic imagery, with most respondents rating this as highly important. People living with rare diseases expressed that seeing “real faces” of those with the condition fosters a sense of connection, combats isolation, and raises public awareness through greater exposure. Conversely, some respondents noted the risk of stereotyping based on appearance, indicating the need for sensitive, accurate portrayal. Our findings suggest that authentic imagery can improve engagement and create an emotional connection with materials, by those living with rare diseases and their communities. Furthermore, we provide actionable recommendations for developers of these materials including patient advocacy groups, research institutions and pharmaceutical companies.
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