Patient COUNTS: A pilot navigation program for Asian American cancer patients.

IF 2.4 4区 心理学 Q1 ETHNIC STUDIES Asian American Journal of Psychology Pub Date : 2024-09-01 DOI:10.1037/aap0000319
Janet N Chu, Janice Y Tsoh, Salma Shariff-Marco, Laura Allen, Debora Oh, Mei-Chin Kuo, Ching Wong, Hoan Bui, Junlin Chen, Angeline Truong, Katarina Wang, Andrea Hwang, Feng Ming Li, Carmen Ma, Scarlett L Gomez, Tung T Nguyen
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Abstract

Many Asian American cancer patients face barriers to cancer care but little is known about their navigational needs. We designed and implemented a pilot study to provide culturally- and linguistically-appropriate navigation for Asian American cancer patients. We recruited Asian American adults age 21+ years, who spoke English, Cantonese, Mandarin, or Vietnamese, with newly diagnosed, stage I-III colorectal, liver, or lung cancer in the Northern California Bay Area. Participants were assigned a language-concordant patient navigator, who provided support and resources over 6 months. Surveys were administered at baseline, 3-, and 6-months to assess sociodemographic characteristics, healthcare access, quality of life (FACT-G), and cancer care needs. Participants' mean age was 65 years (range 38-81); 62% were men, 67% spoke Chinese, and 75% reported limited English proficiency. Forty-two percent of participants had lung, 38% colorectal, and 21% liver cancer. Of 24 participants who enrolled, 67% completed the program and 75% completed standard of care cancer treatment. The average total FACT-G score was 72.6 (SD 17) at baseline, 68.0 (SD 20) at 3 months, and 69.9 (SD 22) at 6 months. All participants reported that the program was culturally appropriate and would recommend it. Asian American cancer patients in a patient navigation program reported lower quality of life compared to the general adult cancer population. Even with navigation, 75% of participants reported completing standard of care treatment. While participants were satisfied with the program, more research is needed to address the quality of cancer care Asian American cancer patients receive.

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患者重要:针对亚裔美国人癌症患者的试点导航计划。
许多美籍亚裔癌症患者面临癌症治疗的障碍,但对他们的导航需求却知之甚少。我们设计并实施了一项试点研究,为美籍亚裔癌症患者提供文化和语言上适宜的导航。我们在北加州湾区招募了 21 岁以上、讲英语、粤语、普通话或越南语的亚裔成人,他们都是新诊断的 I-III 期结直肠癌、肝癌或肺癌患者。参与者被指派了一名语言一致的患者导航员,由其在 6 个月内提供支持和资源。在基线、3 个月和 6 个月时进行了调查,以评估社会人口特征、医疗保健获取途径、生活质量(FACT-G)和癌症护理需求。参与者的平均年龄为 65 岁(38-81 岁不等);62% 为男性,67% 讲中文,75% 表示英语水平有限。42%的参与者患有肺癌,38%患有结肠直肠癌,21%患有肝癌。在 24 名参加者中,67% 的人完成了项目,75% 的人完成了标准癌症治疗。FACT-G 的平均总分基线为 72.6 分(标准差 17 分),3 个月时为 68.0 分(标准差 20 分),6 个月时为 69.9 分(标准差 22 分)。所有参与者都认为该项目符合他们的文化背景,并愿意推荐该项目。与普通成年癌症患者相比,参加患者导航计划的亚裔癌症患者的生活质量较低。即使有了导航,仍有 75% 的参与者表示完成了标准护理治疗。虽然参与者对该项目表示满意,但还需要进行更多的研究,以了解亚裔美国癌症患者所接受的癌症护理的质量。
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来源期刊
CiteScore
3.40
自引率
6.70%
发文量
57
期刊最新文献
A Community-Based Cervical Cancer Education and Navigation Program for Korean American Women. Patient COUNTS: A pilot navigation program for Asian American cancer patients. Developing the Meaning-Centered Program for Chinese Americans with Advanced Cancer: Applying Cultural Adaptation Frameworks. Healthcare Professionals' Views of Supportive Care Needs for Chinese, Korean, and Vietnamese Americans with Metastatic Cancer. Socioeconomic Status, Stress, and Cancer-related Fatigue among Chinese American Breast Cancer Survivors: The Mediating Roles of Sleep.
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