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Journal of Cancer Education

, Volume 31, Issue 3, pp 430–442 | Cite as

Young Adult Cancer Survivors’ Experience with Cancer Treatment and Follow-Up Care and Perceptions of Barriers to Engaging in Recommended Care

  • Carla J. BergEmail author
  • Erin Stratton
  • Natia Esiashvili
  • Ann Mertens
Article

Abstract

We examined correlates of low engagement in the healthcare system, experiences with survivorship care, barriers to follow-up care, and potential resources for promoting follow-up care among young adult survivors of childhood cancers. We conducted a mixed-method study involving surveys of 106 survivors of childhood cancer aged 18–34 recruited from a university-affiliated children’s hospital and an NCI-designated cancer center in the Southeastern USA. Phone-based semistructured interviews were then conducted in a subset of 26. Assessments included health factors, psychosocial factors, healthcare system interaction, and interest in resources to promote engagement in healthcare. Survey participants were on average 22.14 (SD = 3.16) years old, 50.0 % female, and 77.4 % White. Overall, 46.0 % had attended survivorship clinic, 47.2 % reported receiving a treatment summary, 68.9 % had a primary care provider, and 17.0 % reported no interaction with healthcare in the past 2 years. Correlates of less than annual healthcare provider visits included being older (p = 0.003), being male (p < 0.001), lack of insurance (p = 0.002), and having had chemotherapy (p = 0.05). Participants reported varied experiences in terms of how health and treatment information was presented, from none or too little to overwhelming or anxiety-provoking amounts. Barriers to engaging in survivorship care included no/limited insurance, time, or transportation; major life changes; anxiety; and difficulty transitioning from pediatrics to adult care. Participants highlighted the need for educational and psychosocial resources, particularly technology-based resources. Multilevel interventions are needed to increase engagement in survivorship care among young adult cancer survivors. Technology-based resources addressing social support and mental well-being are intervention possibilities.

Keywords

Survivorship care plans Transition to survivorship Young adults Childhood cancer 

Notes

Acknowledgments

This work was supported by the Georgia Cancer Coalition (PI: Berg), the National Cancer Institute (PI: Berg;5K07CA139114), the Emery Egleston Children’s Research Center (PI: Esiashvili), and the Winship CancerInstitute Kennedy Survivorship Award (PI: Berg)

Conflict of Interest

The authors declare no conflict of interest.

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Copyright information

© American Association for Cancer Education 2015

Authors and Affiliations

  • Carla J. Berg
    • 1
    Email author
  • Erin Stratton
    • 1
  • Natia Esiashvili
    • 2
  • Ann Mertens
    • 3
  1. 1.Department of Behavioral Sciences and Health EducationEmory University School of Public HealthAtlantaUSA
  2. 2.Department of Radiology, School of Medicine, Woodruff Health Sciences CenterEmory UniversityAtlantaUSA
  3. 3.Aflac Cancer Center/Department of Pediatrics, Department of Oncology, School of Medicine, Woodruff Health Sciences CenterEmory UniversityAtlantaUSA

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