| Literature DB >> 26681427 |
Abby R Rosenberg1,2,3,4, Kira Bona5,6,7, Claire M Wharton1,2, Miranda Bradford2, Michele L Shaffer2,4, Joanne Wolfe5,7,8, Kevin Scott Baker1,2,4,9.
Abstract
Conducting patient-reported outcomes research with adolescents and young adults (AYAs) is difficult due to low participation rates and high attrition. Forty-seven AYAs with newly diagnosed cancer at two large hospitals were prospectively surveyed at the time of diagnosis and 3-6 and 12-18 months later. A subset participated in 1:1 semistructured interviews. Attrition prompted early study closure at one site. The majority of patients preferred paper-pencil to online surveys. Interview participants were more likely to complete surveys (e.g., 93% vs. 58% completion of 3-6 month surveys, P = 0.02). Engaging patients through qualitative methodologies and using patient-preferred instruments may optimize future research success.Entities:
Keywords: Adolescent and Young Adult Oncology (AYA); health-services research; patient-reported outcomes; pediatric cancer
Mesh:
Year: 2015 PMID: 26681427 PMCID: PMC4755794 DOI: 10.1002/pbc.25843
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167