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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
  • , Iva Strnadová
  • , Julie Loblinzk
  • , Michael David
  • , Ee Lin Chang
  • , Allison Carter
  • , Sally Sweeney
  • , Lauren Winkler
  • , Rosalie Power
  • , Caroline Basckin
  • , Elizabeth Kennedy
  • , Heather Jolly
  • The University of Sydney
  • University of New South Wales
  • Self Advocacy Sydney
  • Griffith University Queensland
  • Family Planning NSW
  • Simon Fraser University

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)
55 Downloads (Pure)

Abstract

Introduction: 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. Methods: 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. Outcomes and analysis: 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.Discussion: 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.
Original languageEnglish
Article number1360447
Number of pages15
JournalFrontiers in Public Health
Volume12
DOIs
Publication statusPublished - 2024

Bibliographical note

Publisher Copyright:
Copyright © 2024 Bateson, Ussher, Strnadová, Loblinzk, David, Chang, Carter, Sweeney, Winkler, Power, Basckin, Kennedy and Jolly.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • accessible information
  • cervical screening
  • co-production
  • inequity
  • intellectual disability
  • self-collection HPV test
  • trauma informed care

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