Design and methods of a multi-level intervention to improve adherence to childhood cancer survivorship care by partnering with primary care providers: The BRIDGES randomized controlled trial

被引:0
作者
Ross, Wilhelmenia L. [1 ]
Santiago-Rivera, Yaiomy [1 ]
Tan, Ming T. [2 ]
Roy, Megan M. [1 ]
Bryant, Stacy [1 ]
Appel, Burton E. [3 ]
Casillas, Jacqueline [4 ]
Demedis, Jenna [5 ]
Smitherman, Andrew B. [6 ]
Horwitz, Leora I. [7 ]
Hurtado-de-Mendoza, Alejandra [1 ]
Mendoza, Jason A. [8 ,9 ,10 ]
Santacroce, Sheila J. [6 ]
Kadan-Lottick, Nina S. [1 ]
机构
[1] Georgetown Lombardi Comprehens Canc Ctr, Washington, DC USA
[2] Georgetown Univ, Dept Biostat Bioinformat & Biomath, Washington, DC 20007 USA
[3] Hackensack Univ Med Ctr, Joseph M Sanzari Childrens Hosp, Childrens Canc Inst, Hackensack, NJ USA
[4] Univ Calif Los Angeles, Los Angeles, CA USA
[5] Univ Colorado, Sch Med, Dept Pediat, Div Hematol Oncol BMT, Aurora, CO USA
[6] Univ North Carolina, Chapel Hill, NC USA
[7] New York Univ, Grossman Sch Med, New York, NY USA
[8] Fred Hutchinson Canc Ctr, Seattle, WA USA
[9] Seattle Childrens Res Inst, Ctr Child Hlth Behav & Dev, Seattle, WA USA
[10] Univ Washington, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
Survivors of childhood cancer; Survivorship care; Randomized controlled trial; Primary care; Patient handoff; Telehealth; Patient compliance; YOUNG-ADULT SURVIVORS; TERM-FOLLOW-UP; MULTIPLE IMPUTATION; PATIENT ACTIVATION; HEALTH-CARE; KNOWLEDGE; COMMUNICATION; SBAR; PERSPECTIVES; PREFERENCES;
D O I
10.1016/j.cct.2025.107859
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Despite heightened risk of chronic health conditions, <20 % of childhood cancer survivors (CCS) receive guideline-recommended surveillance for late effects. Barriers include avoidance of reminders, lack of knowledge, and costs. The goal of the BRIDGES Study is to evaluate the effects of a multi-level, remote intervention on adherence to guideline-recommended surveillance among CCS by partnering with primary care providers (PCPs). Methods: This ongoing study is a multi-site, two-arm, prospective, parallel design, 1:1 randomized controlled non-inferiority trial (N = 240; n = 120/group). Eligibility criteria are: cancer diagnosis at age < 21 years, 2.0-4.0 years post-cancer therapy, and no previous specialty survivorship clinic care. The intervention includes: 1) patient survivorship education via telehealth with a cancer center nurse, including discussion of patient's individualized survivorship care plan (SCP), 2) ongoing patient-tailored health education within the electronic health record's patient portal, 3) a structured interactive phone call between the cancer center nurse and PCP, including discussion of patient's SCP, and 4) an in-person PCP visit for survivorship care. Patients randomized to the comparison group are contacted to schedule an in-person visit at their cancer center-based survivorship clinic. Adherence to guideline-recommended surveillance tests (primary outcome) is assessed at 1-year post-randomization (primary follow-up time point) and 2-years post-randomization (for durability). Patient knowledge, self-efficacy, and activation; PCP knowledge and self-efficacy; and process outcomes are also assessed. Conclusion: Models of survivorship care that overcome existing barriers are needed. If efficacious, this scalable, remote intervention would be a valuable strategy to address barriers and bridge gaps in care to reach more CCS.
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页数:8
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