Optimizing risk‐reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person‐based approach: A think‐aloud interview study
Lynch syndrome "carriers" carry a germline pathogenic variant conferring gene-, sex-, and organ-specific increased cancer risks. They are presented with difficult, interrelated choices over their lifetime. This study was part of a larger project to codesign a health intervention, Lynch Choices™ https://canchoose.org.uk to provide an information hub and decision support for carriers, their family members, and clinicians. This study aimed to answer the research question: What content, framing, and design elements of a decision aid for genetic cancer risk management are important to Lynch syndrome carriers? Adult carriers were invited to a think-aloud interview to hear their thoughts about a prototype version of Lynch Choices™ containing values-clarification exercises. The first half of interviews focused on the gynecological risk-reducing surgery and the second half on the aspirin decision aid. Twenty carriers (eight men) were interviewed, half of whom had a personal history of cancer. Iterative refinement of Lynch Choices™ content and design was completed between interviews using a transparent table of changes from the person-based approach. Following the interviews, reflexive thematic analysis was applied to the entire qualitative dataset. Three themes were constructed to guide further optimization and make recommendations for improved cancer risk communication in clinical practice. The three themes were: (1) Interpreting gene-specific cancer risks and "What does it mean to me?"; (2) Words matter: Careful phrasing is important to feel understood; (3) Decision aids: They can help but might trigger emotions. Think-aloud interviews provided in-depth insight into the psychosocial context of carriers. This informed optimization of the decision aid to support engagement and promote shared decision making with healthcare professionals. The learning from this study had broader implications beyond decision aid development, to understanding preferences, needs, and experiences regarding genetic cancer risk communication and decision support.
Authors
- Elizabeth Bancroft (ORCID: https://orcid.org/0000-0002-5482-5660)
- Emma J. Crosbie (ORCID: https://orcid.org/0000-0003-0284-8630)
- Mev Dominguez–Valentin (ORCID: https://orcid.org/0000-0001-7856-0057)
- Helen Hanson (ORCID: https://orcid.org/0000-0002-3303-8713)
- Mary Jane Esplen (ORCID: https://orcid.org/0000-0002-6034-2235)
- John Burn (ORCID: https://orcid.org/0000-0002-9823-2322)
- Neil Ryan (ORCID: https://orcid.org/0000-0003-3117-3257)
- Lesley Turner (ORCID: https://orcid.org/0000-0003-1489-3471)
- Katherine Morton (ORCID: https://orcid.org/0000-0002-6674-0314)
- Kelly Kohut (ORCID: https://orcid.org/0000-0002-9852-2872)
- Katie M.G. Snape (ORCID: https://orcid.org/0000-0002-1739-7986)
- Pål Møller (ORCID: https://orcid.org/0000-0001-8211-8237)
- Rebecca H. Foster (ORCID: https://orcid.org/0000-0003-4335-8144)
- Karen Hurley
Institutions
- Oslo University Hospital (NO)
- Cleveland Clinic (US)
- Royal Marsden NHS Foundation Trust (GB)
- Institute of Cancer Research (GB)
- Tampere University of Applied Sciences (FI)
- University of Toronto (CA)
- University of Exeter (GB)
- St George’s University Hospitals NHS Foundation Trust (GB)
- Edinburgh Royal Infirmary (GB)
- St Mary's Hospital (GB)
- MRC Centre for Regenerative Medicine (GB)
- MRC Centre for Reproductive Health (GB)
- Tampere University Hospital (FI)
- Tampere University (FI)
- The Patients Association (GB)
- University of Southampton (GB)
- Newcastle University (GB)
- University of Edinburgh (GB)
Publication Details
- Journal
- Journal of Genetic Counseling
- Published
- 2025-08-01
- DOI
- https://doi.org/10.1002/jgc4.70089
- Citations
- 4
- Primary Topic
- Genetic factors in colorectal cancer
- Type
- article
- Field-Weighted Citation Impact
- 5.89
Funders
- Cancer Research UK
- National Institute for Health and Care Research
- University of Southampton
- Manchester Biomedical Research Centre