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Co-producing research study recruitment strategies with and for children and young people for paediatric chronic pain studies.
Ghio, Daniela; Lunt, Laura E; Bridges, Angharad; Gahr, Lydia; Hood, Anna M.
Affiliation
  • Ghio D; Division of Psychology and Mental Health, Faculty of Biology, Medicine and Health, School of Health Science, The University of Manchester, Manchester, United Kingdom.
  • Lunt LE; Centre for Musculoskeletal Research, Versus Arthritis Centre for Epidemiology, The University of Manchester, Manchester, United Kingdom.
  • Bridges A; Manchester Academic Health Science Centre, National Institute of Health Research Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Gahr L; A National Advisory Group of the Barbara Ansell National Network for Adolescent Rheumatology, Your Rheum, Manchester, United Kingdom.
  • Hood AM; A National Advisory Group of the Barbara Ansell National Network for Adolescent Rheumatology, Your Rheum, Manchester, United Kingdom.
Front Pain Res (Lausanne) ; 5: 1358509, 2024.
Article in En | MEDLINE | ID: mdl-39109242
ABSTRACT

Introduction:

Children and young people experiencing chronic pain are at greater risk of inequitable and poor-quality pain management, which has implications for future management of pain in adulthood. Most chronic pain research is conducted with adults who are more likely to be middle-class, white and monocultured. Inclusive and diverse recruitment practices in paediatric pain research can be an area in which we can address this imbalance of representation. The aim of this current work was to explore these practices and to co-produce recommendations regarding recruitment strategies for paediatric pain research.

Methods:

The research team worked with Your Rheum, a United Kingdom young person's advisory group (ages 11-24 years) and diagnosed with rheumatic condition(s), the opportunity to input into rheumatology research. At a virtual Your Rheum meeting, eight young people (female = 7, male = 1, age range 12-24) took part in group discussions, sharing their experiences of taking part in research and their decision process. Online tools, including Mentimeter and Miro, were used to aid conversations and share ideas.

Results:

Most young people had experience of taking part in research as a study participant (n = 5). Recommendations synthesised included increased awareness of research in general. The young people discussed being open to hearing about research opportunities; they reflected that they are rarely exposed to these invitations or hear about current research. The clinic environment was highlighted as a "good and trustworthy" recruitment area - being approached by a member of the research team was considered ideal, even if it was someone they had not met previously. Many young people recalled little discussions of research at their clinical appointments. Deciding to participate in research included the following considerations benefit/impact; connecting with others; research topic; which is then balanced against convenience, and reimbursement. The young people felt that taking part in research was empowering and helped them take ownership of their pain management.

Conclusion:

It is essential to understand the perspectives of potential study participants, to plan successful recruitment strategies. Ensuring we consider these factors when designing our studies and recruitment strategies is beneficial to all involved. Co-produced recruitment strategies would aid inclusive (and increased) research participation.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pain Res (Lausanne) Year: 2024 Document type: Article Affiliation country: United kingdom Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pain Res (Lausanne) Year: 2024 Document type: Article Affiliation country: United kingdom Country of publication: Switzerland