American Indian Or Alaska Native

美洲印第安人或阿拉斯加原住民
  • 文章类型: Journal Article
    目的:在COVID-19大流行的第二年,研究司法参与状况对非老年人院内死亡率的影响。
    方法:这项回顾性队列研究使用了来自美国20个州的2021个州住院数据库(SID)的数据,其中包括住院至少24小时的18-64岁成年人从普通急性护理医院出院.主要结果是全因住院死亡率,主要比较是司法参与状况。我们使用逻辑回归估计优势比(OR)和95%置信区间(CI),随着社会人口因素的调整,Elixhauser合并症,COVID-19诊断,入院敏锐度,其他临床特征,大都市区和季节性。我们将数据随机分成50%的训练和50%的验证集。对于后者,我们评估了我们最终模型的性能。
    结果:研究人群包括4,712,441例出院(1.1%涉及司法;平均[SD]年龄47.5[12.8]岁;47.0%的女性;63.6%的白人,21.8%黑色,11.8%西班牙裔,1.8%亚洲/太平洋岛民[API],和1.0%美洲印第安人/阿拉斯加原住民[AIAN])。其中,发生102,735例住院死亡(2.2%)。在多变量分析中,在涉及司法的患者中,院内死亡率降低约40%(OR0.6,95%CI0.5~0.7,P值<0.01).最终验证的模型显示出出色的区分(受试者操作员特征0.953,95CI0.952至0.954的曲线下面积[AUC])和良好的校准(Brier评分0.014,校准带P值0.186)。
    结论:在这项队列研究中,司法参与状态与较低的住院死亡率独立相关.未来的研究应该检查入院前和出院后的结果。
    OBJECTIVE: To examine the role of justice-involved status on in-hospital mortality among nonelderly adults during the second year of the COVID-19 pandemic.
    METHODS: This retrospective cohort study used data from the 2021 State Inpatient Databases (SIDs) for 20 US states, which included discharges from general acute care hospitals among adults aged 18-64 years hospitalized for at least 24 hours. The main outcome was all-cause in-hospital mortality and the primary comparison was justice-involved status. We used logistic regression to estimate the odds ratios (ORs) and 95% confidence intervals (CIs), with adjustment for sociodemographic factors, Elixhauser comorbidities, COVID-19 diagnosis, admission acuity, other clinical features, metropolitan area and seasonality. We randomly split the data into a 50% training and 50% validation set. With the latter, we evaluated the performance of our final model.
    RESULTS: The study population included 4,712,441 discharges (1.1% justice-involved; mean [SD] age 47.5 [12.8] years; 47.0% women; 63.6% White, 21.8% Black, 11.8% Hispanic, 1.8% Asian/Pacific Islander [API], and 1.0% American Indian/Alaska Native [AIAN]). Among these, 102,735 in-hospital deaths (2.2%) occurred. In the multivariate analysis, in-hospital mortality was about 40% less likely among justice-involved patients (OR 0.6, 95% CI 0.5 to 0.7, P-value < 0.01). The final validated model showed excellent discrimination (area under the curve [AUC] for the receiver operator characteristic 0.953, 95%CI 0.952 to 0.954) and good calibration (Brier score 0.014, calibration belt P-value 0.186).
    CONCLUSIONS: In this cohort study, justice-involved status was independently associated with lower in-hospital mortality. Future studies should examine pre-admission and post-discharge outcomes.
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  • 文章类型: Letter
    暂无摘要。
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  • 文章类型: Journal Article
    加强社会支持和联系可以降低自杀风险,然而,很少有研究在美洲印第安人和阿拉斯加原住民(AI/AN)成年人中检查这种影响。我们评估了自杀意念和行为,受挫的归属感,社会支持,养成文化,历史创伤,来自五个AI/AN社区的709名具有自杀风险的AI/AN成年人的创伤性生活事件。自杀意念与受挫的归属感有关,并受到社会支持和参与AI/AN仪式的保护。在那些终生自杀未遂的人中,创伤性生活事件,由于历史创伤引起的抑郁/焦虑症状,受挫的归属感与更多的尝试有关。更多地参与文化习俗与更少的自杀企图有关。更高水平的社会支持与更多的自杀企图有关,这可能归因于研究的横断面性质。干预措施应侧重于保护因素和针对特定环境的干预措施,强调社区历史,值,和优势。
    Enhancing social support and connectedness can reduce suicide risk, yet few studies have examined this effect in American Indian and Alaska Native (AI/AN) adults. We assessed suicidal ideation and behavior, thwarted belongingness, social support, enculturation, historical trauma, and traumatic life events in 709 AI/AN adults at high risk of suicide from five AI/AN communities. Suicidal ideation was associated with thwarted belongingness and protected against by social support and engaging in AI/AN ceremonies. Among those who made lifetime suicide attempts, traumatic life events, symptoms of depression/anxiety due to historical trauma, and thwarted belongingness were linked to more attempts. More engagement in cultural practices was associated with fewer suicide attempts. Higher levels of social support were associated with more suicide attempts, an observation potentially attributable to the cross-sectional nature of the study. Interventions should focus on protective factors and context-specific interventions emphasizing community history, values, and strengths.
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  • 文章类型: News
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  • 文章类型: Journal Article
    了解涉及司法系统的人群之间的死亡率差异对于公共卫生和政策至关重要,特别是对于边缘化种族群体,如美洲印第安人/阿拉斯加原住民。
    为了研究南达科他州涉及更广泛的司法系统的人口中死亡率的种族差异,注重不同的量刑倾向和作用场所。
    这项观察性研究使用了2000年1月至2016年12月与死亡率数据相关的行政犯罪记录。全州范围内的数据与南达科他州总检察长办公室和南达科他州卫生部的数据相关联。在这个基于人群的样本中分析了18岁及以上的被捕者。数据从2022年8月1日至2023年7月30日进行了分析。
    仅将判刑处置归类为逮捕,好,缓刑,监狱,还有监狱.
    主要结果是使用泊松回归模型计算的死亡率(包括全因和特定原因),根据人口和县级变量进行了调整。
    在182472个人中,有422987人被捕,研究样本包括29690名美洲印第安人/阿拉斯加原住民被捕者(男性17900[60%];平均[SD]年龄,29.4[11.0]岁)和142248名白人被捕者(103471[73%]男性;平均[SD]年龄,32.6[12.9]年)。美洲印第安人/阿拉斯加原住民占被捕者的16%,占被捕者的26%,但只有9%的人口在南达科他州。跨配置,白人被判缓刑的死亡风险更大,监狱,和监狱相对于只被捕的白人。在种族差异方面,在仅逮捕处置中,美洲印第安人/阿拉斯加原住民的全因死亡风险是白人被捕者的2.37倍(95%CI,1.95-2.88).在所有处置中都存在差异,但在缓刑和监禁方面却大大缩小了差异。原因特异性死亡风险的结果相似,除了癌症风险。在城市地区,在仅有逮捕倾向的人群中,相对于白人个体,美洲印第安人/阿拉斯加原住民的死亡风险高2.70倍(95%CI,1.29-2.44).
    在这项基于人群的观察研究中,涉及司法系统的个人之间的死亡风险和相关种族差异在性格和地点上有很大差异,强调需要针对这些因素进行公共卫生干预。需要进一步的研究来了解量刑和地点塑造这些差异的机制。
    UNASSIGNED: Understanding mortality disparities among justice system-involved populations is crucial for public health and policy, especially for marginalized racial groups such as American Indian/Alaska Native persons.
    UNASSIGNED: To examine racial disparities in mortality within the broader justice system-involved population in South Dakota, focusing on different sentencing dispositions and the role of place.
    UNASSIGNED: This observational study used administrative criminal records linked to mortality data from January 2000 to December 2016. The statewide data linked data from South Dakota Attorney General\'s Office and South Dakota Department of Health. Individuals aged 18 years and older with arrests were analyzed in this population-based sample. Data were analyzed from August 1, 2022, to July 30, 2023.
    UNASSIGNED: Sentencing dispositions were categorized as arrest only, fine, probation, jail, and prison.
    UNASSIGNED: The main outcomes were mortality rates (both all-cause and cause-specific) calculated using Poisson regression models, adjusted for demographic and county variables.
    UNASSIGNED: Of 182 472 individuals with 422 987 arrests, the study sample included 29 690 American Indian/Alaska Native arrestees (17 900 [60%] male; mean [SD] age, 29.4 [11.0] years) and 142 248 White arrestees (103 471 [73%] male; mean [SD] age, 32.6 [12.9] years). American Indian/Alaska Native persons accounted for 16% of arrestees and 26% of arrests, but only 9% of the population in South Dakota. Across dispositions, mortality risk was greater for White individuals sentenced to probation, jail, and prison relative to White individuals who were arrested only. In terms of racial disparities, all-cause mortality risk was 2.37 (95% CI, 1.95-2.88) times higher for American Indian/Alaska Native than White arrestees in the arrest-only disposition. Disparities persisted across all dispositions but narrowed substantially for probation and prison. Results were similar for cause-specific mortality risk, except for cancer risk. In urban areas, mortality risk was 2.70 (95% CI, 1.29-2.44) times greater for American Indian/Alaska Native individuals relative to White individuals among those with arrest-only dispositions.
    UNASSIGNED: In this population-based observational study, mortality risk and associated racial disparities among justice system-involved individuals differed substantially across dispositions and places, underscoring the need for public health interventions tailored to these factors. Further research is needed to understand the mechanisms through which sentencing and place shape these disparities.
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  • 文章类型: Journal Article
    过度限制的临床试验资格标准会降低普遍性,注册慢,不成比例地排除了历史上代表性不足的人口。分析了由国家老龄化研究所资助的196项阿尔茨海默病和相关痴呆(AD/ADRD)试验的资格标准,以确定共同标准及其可能按种族/民族不成比例地排除参与者。试验按类型分类(48期I/II药理学,7III/IV期药理学,128非药理学,7诊断,和6个神经精神病学)和目标人群(51个AD/ADRD,58轻度认知障碍,25有风险,和62认知正常)。合格标准被编码为以下类别:医疗,神经学,精神病,和程序。进行了文献检索,以描述非洲裔美国人/黑人(AA/B)的资格标准差异的普遍性,西班牙裔/拉丁裔(H/L),美洲印第安人/阿拉斯加原住民(AI/AN)和夏威夷原住民/太平洋岛民(NH/PI)人口。试验的中位数为15个标准。最常见的标准是年龄截止(87%的试验),指定的神经系统(65%),和精神疾病(61%)。代表性不足的群体可能会被16个资格类别不成比例地排除在外;42%的试验仅在其标准中指定了讲英语的人。大多数试验(82%)包含操作性较差的标准(即,没有明确定义的标准,可以有多种解释/实施方式)和可能减少种族/族裔入学多样性的标准。
    Overly restrictive clinical trial eligibility criteria can reduce generalizability, slow enrollment, and disproportionately exclude historically underrepresented populations. The eligibility criteria for 196 Alzheimer\'s Disease and Related Dementias (AD/ADRD) trials funded by the National Institute on Aging were analyzed to identify common criteria and their potential to disproportionately exclude participants by race/ethnicity. The trials were categorized by type (48 Phase I/II pharmacological, 7 Phase III/IV pharmacological, 128 non-pharmacological, 7 diagnostic, and 6 neuropsychiatric) and target population (51 AD/ADRD, 58 Mild Cognitive Impairment, 25 at-risk, and 62 cognitively normal). Eligibility criteria were coded into the following categories: Medical, Neurologic, Psychiatric, and Procedural. A literature search was conducted to describe the prevalence of disparities for eligibility criteria for African Americans/Black (AA/B), Hispanic/Latino (H/L), American Indian/Alaska Native (AI/AN) and Native Hawaiian/Pacific Islander (NH/PI) populations. The trials had a median of 15 criteria. The most frequent criterion were age cutoffs (87% of trials), specified neurologic (65%), and psychiatric disorders (61%). Underrepresented groups could be disproportionately excluded by 16 eligibility categories; 42% of trials specified English-speakers only in their criteria. Most trials (82%) contain poorly operationalized criteria (i.e., criteria not well defined that can have multiple interpretations/means of implementation) and criteria that may reduce racial/ethnic enrollment diversity.
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  • 文章类型: Journal Article
    目标:美国矫正人群按种族/民族划分的丙型肝炎病毒(HCV)护理级联数据很少。
    目的:以种族/民族评估国家矫正人群的HCV护理级联。
    方法:这项回顾性队列研究使用了康涅狄格州矫正部门的数据,诊断,并在2019年至2023年期间使用直接作用抗病毒药物(DAAs)治疗慢性HCV感染。
    方法:HCV护理级联结果,包括测试,治疗,和治愈率,按种族/民族进行比较。泊松回归用于估计患病率比率(PRs),调整人口和法律地位因素。
    结果:共有24,867名患者进行了HCV检测(男性占88.9%,平均(SD)年龄35.6(11.8),32.7%白色,37.9%黑色,28.4%的西班牙裔,0.6%亚洲人,0.4%美洲印第安人/阿拉斯加原住民(AIAN),34.7%被判刑≥1年)。HCV暴露和慢性HCV在白人中最高(27.1%和15.2%),在黑人个体中最低(4.6%和2.6%)(P<0.01,对于两种结果)。在被监禁期间,63.2%的慢性HCV患者开始DAA,不同种族/民族的治疗率无显著差异(P>0.05)。对于那些接受治疗并有治疗后实验室数据的人,所有种族/民族的治愈率均为98.8%或更高(P>0.05)。在调整后的回归分析中,对于那些被判刑<1年的人,丙肝治疗的开始率较低(PR,0.76;95%CI,0.67-0.87)和未判刑(PR,0.85;95%CI,0.80-0.91)比被判刑≥1年的人。调整后的晚期纤维化分期/活动度的患病率与种族/民族无关。
    结论:在这项队列研究中,不到三分之二的慢性HCV患者在监禁期间开始DAA治疗,对于那些有可用数据的人来说,几乎都被治愈了。虽然在HCV暴露和慢性HCV感染方面存在差异,未观察到治疗开始率或治愈率的显著种族/民族差异.需要进一步努力增加HCV治疗,特别是对于监禁期较短的患者。
    OBJECTIVE: Hepatitis C virus (HCV) care cascade data by race/ethnicity for US correctional populations are sparse.
    OBJECTIVE: To evaluate the HCV care cascade by race/ethnicity for a state correctional population.
    METHODS: This retrospective cohort study used Connecticut Department of Correction data for incarcerated individuals tested, diagnosed, and treated for chronic HCV infection with direct-acting antivirals (DAAs) from 2019 to 2023.
    METHODS: HCV care cascade outcomes, including testing, treatment, and cure rates, were compared by race/ethnicity. Poisson regression was used to estimate prevalence ratios (PRs), with adjustment for demographic and legal status factors.
    RESULTS: A total of 24,867 patients tested for HCV (88.9% men, mean (SD) age 35.6 (11.8), 32.7% White, 37.9% Black, 28.4% Hispanic, 0.6% Asian, 0.4% American Indian/Alaska Native (AIAN), 34.7% sentenced ≥ 1 year). Both HCV exposure and chronic HCV were highest for White (27.1% and 15.2%) and lowest for Black individuals (4.6% and 2.6%) (P < 0.01, for both outcomes). While incarcerated, 63.2% of chronic HCV patients started DAAs, and treatment rates did not significantly differ by race/ethnicity (P > 0.05). For those treated and having post-treatment lab data available, cure rates were 98.8% or better for all racial/ethnic groups (P > 0.05). In the adjusted regression analyses, HCV treatment initiation was lower for those sentenced < 1 year (PR, 0.76; 95% CI, 0.67-0.87) and unsentenced (PR, 0.85; 95% CI, 0.80-0.91) than those sentenced ≥ 1 year. The adjusted prevalence of advanced fibrosis stage/activity grade was not significantly associated with race/ethnicity.
    CONCLUSIONS: In this cohort study, less than two-thirds of chronic HCV patients initiated DAA treatment during their incarceration, and for those with available data, nearly all were cured. While there were disparities in HCV exposure and chronic HCV infection, significant racial/ethnic differences were not observed for treatment initiation or cure rates. Further efforts are needed to increase HCV treatment, especially for patients with shorter incarceration periods.
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  • 文章类型: Journal Article
    背景:尽管有历史和当代的创伤,美洲印第安人和阿拉斯加原住民(AIAN;土著)社区对COVID-19大流行做出了反应。然而,AIAN经历了不成比例的感染率,住院治疗,死亡,减少预期寿命。学校关闭加剧了差距,导致学习损失,经济不稳定,和AIAN青年的心理健康挑战。
    方法:SafeSchools项目队列研究采用了综合纵向收敛混合方法,整合基于社区的参与式研究原则。该研究招募了纳瓦霍民族的照顾者,他们的孩子有资格参加当地的预订学校。我们对2021年8月至2022年5月收集的护理人员自我报告基线数据进行了分析。
    结果:共有242名护理人员完成了至少部分基线评估,并纳入数据分析。照顾者主要是女性(88.7%),非西班牙裔(97%),土著(97%)。大多数护理人员都在30多岁(平均年龄38岁),不同的教育背景和就业状况。儿童在男性和女性之间平均分配,并分布在不同年龄段。大多数儿童以各种形式在基线上上学,包括面对面,混合动力车,和仅在线设置。看护者报告了一系列的社会心理和行为风险,包括一般的精神困扰,抑郁症状,对自己和孩子的焦虑。此外,照顾者和儿童表现出各种保护因素,比如强烈的文化认同,弹性,和学业自我效能感。
    结论:这项研究强调了参与的照顾者和儿童的心理健康困扰率高于全国平均水平。尽管面临这些挑战,文化保护因素仍然很强,应该指导未来的危机应对工作。
    BACKGROUND: Despite historical and contemporary trauma, American Indian and Alaska Native (AIAN; Indigenous) communities responded with resilience to the COVID-19 pandemic. However, AIANs experienced disproportionate rates of infection, hospitalization, death, and reduced life expectancy. School closures exacerbated disparities, leading to learning loss, economic instability, and mental health challenges among AIAN youth.
    METHODS: The Project SafeSchools cohort study employed a comprehensive longitudinal convergent mixed-methods approach, integrating community-based participatory research principles. The study enrolled Navajo Nation caregivers whose children were eligible to attend local reservation-based schools. We conducted an analysis of caregiver self-report baseline data collected between August 2021 and May 2022.
    RESULTS: A total of 242 caregivers completed at least part of the baseline assessment and were included in data analysis. Caregivers were primarily female (88.7%), non-Hispanic (97%), and Indigenous (97%). Most caregivers were in their late 30s (mean age 38), with varying educational backgrounds and employment statuses. Children were evenly split between males and females and distributed across different age groups. Most children attended school at baseline in various formats, including in-person, hybrid, and online-only settings. Caregivers reported a range of psychosocial and behavioral risks, including general mental distress, depressive symptoms, and anxiety for themselves and their children. Furthermore, caregivers and children exhibited various protective factors, such as strong cultural identity, resilience, and academic self-efficacy.
    CONCLUSIONS: This study highlights the higher rates of mental health distress among participating caregivers and children compared to national averages. Despite these challenges, cultural protective factors remained strong and should guide future crisis response efforts.
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  • 文章类型: Journal Article
    先前的研究表明,在文化上是一致的,可获得和低障碍的干预措施处于有利位置,以符合美国印第安人和阿拉斯加原住民(AI/AN)酒精使用障碍(AUD)患者的需求。考虑到社区成员的建议和COVID-19大流行期间身体距离的需要,我们的团队开发了一个虚拟减害谈话圈子(HaRTC)的协议来整合这些要点.这8周的目标,单臂飞行员最初要记录可行性,可接受性,以及与虚拟HaRTC出勤相关的结果,它集成了虚拟连接的可访问性,低屏障减少伤害的方法,和文化上一致的干预。参与者(N=51)是41个部落成员和25个美国州的AUD(当前或缓解)的AI/AN人。在基线采访之后,参与者被邀请参加8次每周一次的虚拟HaRTC会议.在基线,中点和测试后评估,我们收集了有关虚拟HaRTC可接受性的数据,文化联系,生活质量,酒精的结果。在接近的123人中,63%的人有兴趣并同意参与。参与者平均参加了2.1(SD=2.02)次虚拟HaRTC会议,64%的参与者至少参加了一次。在1到10的范围内,参与者将虚拟HaRTC评为高度可接受(M=9.3,SD=1.9),有效(M=8.4,SD=2.9),文化一致(M=9.2,SD=1.5),有帮助(M=8.8,SD=1.9),并以良好的方式进行(M=9.8,SD=0.5)。尽管单臂研究设计排除了因果关系,参与者在3个时间点的饮酒天数和与酒精相关的伤害方面表现出统计学上显著的减少.此外,两种灵性的感觉,这是文化联系的一个因素,随着时间的推移,与健康相关的生活质量随着参加HaRTC会议次数的增加而增加。VirtualHaRTC显示了作为具有AUD的AI/AN人群的文化一致干预措施的初始可行性和可接受性。未来的随机对照试验将提供这种方法的有效性测试。
    Prior research suggests that culturally aligned, accessible and lower-barrier interventions are well-placed to align with the needs of American Indian and Alaska Native (AI/AN) people with alcohol use disorder (AUD). Taking into account community members\' suggestions and the need for physical distancing during the COVID-19 pandemic, our team developed a protocol for virtual Harm Reduction Talking Circles (HaRTC) to incorporate these points. The aims of this 8-week, single-arm pilot were to initially document feasibility, acceptability, and outcomes associated with attendance at virtual HaRTC, which integrates the accessibility of virtual connection, a lower-barrier harm-reduction approach, and a culturally aligned intervention. Participants (N = 51) were AI/AN people with AUD (current or in remission) across 41 Tribal affiliations and 25 US states. After a baseline interview, participants were invited to attend 8, weekly virtual HaRTC sessions. At the baseline, midpoint and post-test assessments, we collected data on virtual HaRTC acceptability, cultural connectedness, quality of life, and alcohol outcomes. Of the 123 people approached, 63% were interested in and consented to participation. Participants attended an average of 2.1 (SD = 2.02) virtual HaRTC sessions, with 64% of participants attending at least one. On a scale from 1 to 10, participants rated the virtual HaRTC as highly acceptable (M = 9.3, SD = 1.9), effective (M = 8.4, SD = 2.9), culturally aligned (M = 9.2, SD = 1.5), helpful (M = 8.8, SD = 1.9), and conducted in a good way (M = 9.8, SD = 0.5). Although the single-arm study design precludes causal inferences, participants evinced statistically significant decreases in days of alcohol use and alcohol-related harm over the three timepoints. Additionally, both sense of spirituality, which is a factor of cultural connectedness, and health-related quality of life increased over time as a function of the number of HaRTC sessions attended. Virtual HaRTC shows initial feasibility and acceptability as a culturally aligned intervention for AI/AN people with AUD. Future randomized controlled trials will provide a test of the efficacy of this approach.
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  • 文章类型: Journal Article
    尽管美洲印第安人和阿拉斯加原住民(AIAN)的学生是美国在生物医学和健康科学领域相对于人口规模而言代表性最低的群体,对长期研究教育计划和结果跟踪知之甚少。20多年来,美国原住民癌症预防合作伙伴关系(NACP)得到了美国国家癌症研究所(NCI)资助的促进癌症健康平等全面合作伙伴关系(CPACHE)计划的支持。编程包括动手指导研究和一系列发展机会。一个经过验证的跟踪系统,结合了参与记录,机构记录,以及国家学生信息交换所文件的入学/学位成绩。NACP总共(2002-2022年)聘用了367名AIAN学员,其中237个人获得了220个单身汉,87大师,和34个博士/专业学位。大约45%的AIAN博士获得者目前从事学术或临床工作,和10%的行业或部落领导。共有238名AIAN学生参加了指导研究,85%的人表现出强劲的成果;51%获得学位,目前有34%注册。健壮的跟踪系统的实施记录了一段时间内达到程度的加速度。接下来的步骤将评估对学生成绩最有影响力的培训活动。
    Although American Indian and Alaska Native (AIAN) students are the most underrepresented group in the U.S. in biomedical and health sciences relative to population size, little is known about long-term research education programs and outcome tracking. For over 20 years, the Partnership for Native American Cancer Prevention (NACP) has been supported under the National Cancer Institute\'s (NCI)-funded Comprehensive Partnerships to Advance Cancer Health Equity (CPACHE) program. Programming included hands-on mentored research and an array of development opportunities. A validated tracking system combining participation records, institutional records, and enrollment/degree attainment from the National Student Clearinghouse documents outcomes. Collectively (2002-2022) NACP engaged 367 AIAN trainees, of whom 237 individuals earned 220 bachelors, 87 masters, and 34 doctoral/professional degrees. Approximately 45% of AIAN doctoral recipients are currently engaged in academic or clinical work, and 10% in industry or tribal leadership. A total of 238 AIAN students participated in mentored research, with 85% demonstrating strong outcomes; 51% attained a degree, and 34% are currently enrolled. Implementation of a robust tracking system documented acceleration in degree attainment over time. Next steps will evaluate the most impactful training activities on student outcomes.
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