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Adverse childhood experiences (ACEs) and medically traumatic events (TEs) in adolescents and young adults (AYAs) with cancer: a report from the Promoting Resilience in Stress Management (PRISM) randomized controlled trial

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Abstract

Objective

In adolescents and young adults (AYAs) with cancer, we examined (1) the distribution and type of traumatic events (TEs) experienced prior to baseline assessment and (2) how a resilience intervention, Promoting Resilience in Stress Management (PRISM), impacted changes in patient-reported outcomes (PROs) for AYAs with and without TEs.

Methods

AYAs (12–25 years) within 1–10 weeks of diagnosis of new malignancy or ever diagnosed with advanced cancer were enrolled and randomly assigned to usual care (UC) with or without PRISM. To assess TEs, we screened medical records for traditionally defined adverse childhood experiences (ACEs) and medical traumatic events. Age-validated PROs assessed resilience, benefit-finding, hope, generic health-related quality of life (QoL), cancer-specific QoL, depression, and anxiety at enrollment and 6 months later. We calculated effect sizes (Cohen’s d) for PRISM vs. UC effect on PRO score change at 6 months for 1+ TEs and 0 TE groups.

Results

Ninety-two AYAs enrolled and completed baseline surveys (44-UC, 48-PRISM; N = 74 at 6 months, 38-UC, 36-PRISM); 60% experienced 1+ TEs. PROs at baseline were similar across groups. PRISM’s effect on score change was greater (Cohen’s d ≥ 0.5) for the 1+ TE group on domains of benefit-finding and hope; and similar (d < 0.5) on domains of resilience, depression, anxiety, and both generic and cancer-specific QoL.

Conclusions

In AYAs with cancer, TEs occurred at similar rates as the general population. PRISM may be particularly helpful for improving benefit-finding and hope for those who have experienced TEs.

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Data availability

The data that support the findings of this study may be available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

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Acknowledgments

We thank patients and their families for their participation in this study. We also thank Michele Shaffer for her contributions to the statistical design of this trial, and Claire Wharton, Lauren Eaton, Victoria Klein, and Stacy Garcia for their efforts on patient enrollment, data collection and management, intervention administration, and administrative support. We also thank the University of Denver’s Psychology Department Writing Group for their review of early manuscript drafts.

Funding

This work was supported by grants from the National Center for Advancing Translational Sciences of the National Institutes of Health (KL2TR000421) and CureSearch for Children’s Cancer awarded to Dr. Rosenberg.

Author information

Authors and Affiliations

Authors

Contributions

S.R.S. conceptualized and designed the post hoc analysis, drafted the initial manuscript, and reviewed and revised the manuscript. A.G.O. double coded a subsection of medical chart data to reliability, contributed to the post hoc analysis conception and design and data interpretation, critically reviewed and revised the manuscript, and provided approval of the submitted product. M.C.B. conducted the statistical analyses, critically reviewed and revised the manuscript, and approved the submitted product. K.F., N.L., A.S., M.T., J.P.Y.-F., and A.R.R. contributed to the post hoc analysis conception and design and data interpretation, critically reviewed and revised the manuscript, and provided approval of the submitted product. In addition, A.R.R. is the Principal Investigator of the Promoting Resilience in Stress Management (PRISM) randomized clinical trial.

Corresponding author

Correspondence to Abby R. Rosenberg.

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Conflict of interest

The authors declare that they have no conflict of interest.

Ethics approval

The study was approved by the SCH Institutional Review Board (IRB; Protocol No. 15300). This trial is registered at ClinicalTrials.gov (NCT02340884).

Consent to participate

Researchers obtained informed consent from all participants. In cases where participants were under the age of 18, informed consent was obtained from parents/legal guardians and informed assent was obtained from the participant.

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While all data is anonymized, participants provided informed consent for publication of their data.

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Scott, S.R., O’Daffer, A.G., Bradford, M.C. et al. Adverse childhood experiences (ACEs) and medically traumatic events (TEs) in adolescents and young adults (AYAs) with cancer: a report from the Promoting Resilience in Stress Management (PRISM) randomized controlled trial. Support Care Cancer 29, 3773–3781 (2021). https://doi.org/10.1007/s00520-020-05888-x

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