An education resource for human papillomavirus oropharyngeal cancer patients: think-aloud interviews

• Published in: Supportive care in cancer 2023-03, Vol.31 (3), p.158-158, Article 158
• Main Authors: Sharman, Ashleigh R., Ferguson, Eliza M., Dhillon, Haryana M., Macleod, Paula, McCrossin, Julie, Sundaresan, Puma, Clark, Jonathan R., Smith, Megan A., Dodd, Rachael H.
• Format: Article
• Language: English
• Subjects: Cancer patients; Care and treatment; Head & neck cancer; Health psychology; Human papillomavirus; Human Papillomavirus Viruses; Humans; Medicine; Medicine & Public Health; Nursing; Nursing Research; Oncology; Oropharyngeal Neoplasms - psychology; Oropharyngeal Neoplasms - therapy; Pain Medicine; Papillomavirus infections; Papillomavirus Infections - complications; Papillomaviruses; Patient education; Patient satisfaction; Rehabilitation Medicine; Social media; Teaching methods; Throat cancer
• ISSN: 0941-4355; 1433-7339
• DOI: 10.1007/s00520-023-07592-y

Purpose The human papillomavirus (HPV) is well recognised as a factor in developing oropharyngeal cancer (OPC). A booklet for HPV-OPC patients aimed to deliver evidence-based messages in everyday language, in a way to minimise negative psychological impacts on patients. Our study explored the suitability of the booklet for use. Methods Participants were recruited through social media and interviewed via Zoom. Participants were shown the booklet and a think-aloud method elicited real-time reactions to the content. Responses were analysed for each section and coded as either for or against for content, with other responses thematically analysed using NVivo. Results The sample comprised 24 participants: patients ( n = 19) who completed treatment for HPV-OPC and partners of survivors of HPV-OPC ( n = 5). All participants found the booklet useful, and most wished the resource had been available previously. Some indicated the information was new to them. The majority agreed the booklet would be best delivered by their specialist at point of diagnosis and would be a useful resource for friends and family. Most participants gave feedback on improvements to the booklet in terms of comprehension and design. Overall, participants found the content easy to understand. Most participants found that it helped to reduce shame and stigma associated with HPV as a sexually transmitted infection. Conclusion An evidence-based booklet for HPV-OPC patients and their partners is acceptable. Implementation may be feasible in routine clinical practice, specifically at time of diagnosis. Adapting the content will help optimise the efficacy of the booklet in facilitating communication between all stakeholders.