Working together with people with intellectual disability to make a difference: a protocol for a mixed-method co-production study to address inequities in cervical screening participation

Deborah Bateson, Jane Ussher, I. Strnadová, Julie Loblinzk, Michael David, Ee-Lin Chang, Allison Carter, Sally Sweeney, Lauren Winkler, Rosalie Power, Caroline Basckin, Elizabeth Kennedy, Heather Jolly
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Abstract

Cervical cancer is one of the most preventable cancers yet remains a disease of inequity for people with intellectual disability, in part due to low screening rates. The ScreenEQUAL project will use an integrated knowledge translation (iKT) model to co-produce and evaluate accessible cervical screening resources with and for this group.Stage 1 will qualitatively explore facilitators and barriers to screening participation for people with intellectual disability, families and support people, healthcare providers and disability sector stakeholders (n ≈ 20 in each group). An accessible multimodal screening resource, accompanying supporting materials for families and support people, and trauma-informed healthcare provider training materials will then be co-produced through a series of workshops. Stage 2 will recruit people with intellectual disability aged 25 to 74 who are due or overdue for screening into a single-arm trial (n = 48). Trained support people will provide them with the co-produced resource in accessible workshops (intervention) and support them in completing pre-post questions to assess informed decision-making. A subset will participate in qualitative post-intervention interviews including optional body-mapping (n ≈ 20). Screening uptake in the 9-months following the intervention will be measured through data linkage. Family members and support people (n = 48) and healthcare providers (n = 433) will be recruited into single-arm sub-studies. Over a 4-month period they will, respectively, receive the accompanying supporting materials, and the trauma-informed training materials. Both groups will complete pre-post online surveys. A subset of each group (n ≈ 20) will be invited to participate in post-intervention semi-structured interviews.Our primary outcome is a change in informed decision-making by people with intellectual disability across the domains of knowledge, attitudes, and screening intention. Secondary outcomes include: (i) uptake of screening in the 9-months following the intervention workshops, (ii) changes in health literacy, attitudes and self-efficacy of family members and support people, and (iii) changes in knowledge, attitudes, self-efficacy and preparedness of screening providers. Each participant group will evaluate acceptability, feasibility and usability of the resources.If found to be effective and acceptable, the co-produced cervical screening resources and training materials will be made freely available through the ScreenEQUAL website to support national, and potentially international, scale-up.
与智障人士携手改变现状:为解决宫颈筛查参与不平等问题而开展的混合方法共同生产研究协议
宫颈癌是最容易预防的癌症之一,但对于智障人士来说,它仍然是一种不公平的疾病,部分原因是筛查率低。ScreenEQUAL 项目将采用综合知识转化(iKT)模式,与该群体共同制作并评估无障碍宫颈癌筛查资源。第 1 阶段将从定性角度探讨智障人士、家庭和辅助人员、医疗保健提供者和残疾部门利益相关者(每组人数≈20)参与筛查的促进因素和障碍。然后,将通过一系列研讨会共同制作无障碍多模态筛查资源、面向家庭和辅助人员的配套辅助材料以及创伤知情的医疗服务提供者培训材料。第二阶段将招募年龄在 25 至 74 岁之间、即将或逾期接受筛查的智障人士参加单臂试验(n = 48)。经过培训的辅助人员将在无障碍研讨会上向他们提供共同制作的资源(干预),并帮助他们完成事后问题,以评估知情决策。一部分人将参加干预后的定性访谈,包括可选的身体绘图(n ≈ 20)。干预后 9 个月的筛查率将通过数据链接进行测量。家庭成员和支持者(n = 48)以及医疗服务提供者(n = 433)将被纳入单臂子研究。在为期 4 个月的时间里,他们将分别收到随附的辅助材料和创伤知情培训材料。两组人员都将完成事前-事后在线调查。我们的主要结果是智障人士的知情决策在知识、态度和筛查意向等方面的变化。次要结果包括我们的主要结果是智障人士的知情决策在知识、态度和筛查意向等方面的变化。次要结果包括:(i) 干预研讨会后 9 个月内的筛查接受率,(ii) 家庭成员和支持者在健康知识、态度和自我效能方面的变化,以及 (iii) 筛查提供者在知识、态度、自我效能和准备程度方面的变化。每个参与小组都将对资源的可接受性、可行性和可用性进行评估。如果发现有效且可接受,将通过 "平等筛查 "网站免费提供共同制作的宫颈癌筛查资源和培训材料,以支持在全国范围内,甚至可能在国际范围内进行推广。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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