Association of a Lay Health Worker-Led Intervention on Goals of Care, Quality of Life, and Clinical Trial Participation Among Low-Income and Minority Adults With Cancer

被引:15
|
作者
Patel, Manali, I [1 ,2 ,3 ]
Khateeb, Sana [1 ]
Coker, Tumaini [4 ,5 ]
机构
[1] Stanford Univ, Div Oncol, Sch Med, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Med Serv, Palo Alto, CA USA
[3] Stanford Univ, Ctr Primary Care & Outcomes Res Hlth Res & Policy, Sch Med, Stanford, CA 94305 USA
[4] Seattle Childrens Res Inst, Seattle, WA USA
[5] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
PALLIATIVE CARE; UNITED-STATES; MEDICAL-CARE; DELIVERY; RACE; EXPERIENCES; DISPARITIES; BARRIERS; WHITE; TRUST;
D O I
10.1200/OP.21.00100
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE New approaches are needed to overcome low supportive care and clinical trial participation among low-income and minority adults with cancer. The objective of this project was to determine whether a lay health worker intervention was associated with improvements in supportive care and trial participation. METHODS We conducted a quality improvement initiative in collaboration with a union organization. We enrolled union members newly diagnosed with cancer into a 6-month lay health worker-led intervention from October 15, 2016, to February 28, 2017. The primary outcome was goals of care. Secondary outcomes were health-related quality of life (HRQOL), health care use, and trial participation. All outcomes except HRQOL were compared with a cohort of union members diagnosed within the 6-month preintervention period. RESULTS Sixty-six adults participated in the intervention group, and we identified 72 adults in the control group. Demographic characteristics were similar between groups. The mean age was 56.0 years; 47 (34%) were male, and 22 were White (16%). Within 6 months enrollment, more intervention group participants, as compared with the control, had clinician-documented goals of care (94% v 26%; P < .001) and participated in cancer clinical trials (72% v22%; P< .001). At 4 months postenrollment, as compared with baseline, intervention participants experienced HRQOL improvements (mean difference, 3.98 points; standard deviation, 2.83; P< .001). Before death, more intervention group participants used palliative care and hospice than the control group. CONCLUSION Lay health worker-led interventions may improve supportive care and clinical trial participation among low-income and minority populations with cancer. (C) 2021 by American Society of Clinical Oncology
引用
收藏
页码:685 / +
页数:11
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