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‘We care about culture, connection, and making girls feel amazing': A program evaluation using the RE-AIM framework “我们关心文化,联系,让女孩感觉很棒”:使用RE-AIM框架的项目评估
Pub Date : 2026-01-23 DOI: 10.1016/j.fnhli.2025.100099
Jenne Roberts , Hayley Longbottom , Cleone Wellington , Sue Kildea , Yu Gao , Lynne Dooley , Betty Smith , Yvette Roe
This study evaluated a health and wellbeing program for First Nations girls and young women implemented by an Aboriginal community-controlled health organisation. The evaluation used the RE-AIM (Reach, Effectiveness, Adoption, Implementation, and Maintenance) framework.
In-depth, semi-structured interviews were conducted with 39 key informants, including program participants and implementers. The program reached 59% of the target group. The design and implementation were grounded in Indigenous philosophies of collective and relational flourishing. Through participation, individuals strengthened connections and established trusting relationships. Storytelling and yarning enabled participants to locate themselves in an ongoing narrative that mapped their family and community history. Schools with aspirations aligned with the program goals adopted it, although implementation was hampered by COVID-19 restrictions. The program applied a sophisticated understanding of strengths-based practice, relationality, and the role of resistance and resilience to meet the participants’ needs.
The evaluation provides evidence supporting the effectiveness of the program and highlights the factors contributing to its success. The findings highlight that effective programs for young women in urban settings embed connection to culture and identity at their core. It illustrates the value of Aboriginal community-controlled service delivery. When implementing or funding similar programs, two main insights should guide decisions. Firstly, the focus must be on cultural continuity and empowerment. Secondly, success depends on removing practical barriers and engaging participants through interactions that are affirming, fun and inspiring.
The leadership and knowledge of Aboriginal collaborators throughout the research and writing process were key to producing a rigorous and relevant evaluation.
本研究评估了由土著社区控制的卫生组织为第一民族女孩和年轻妇女实施的健康和福利计划。评估使用了RE-AIM(达到、有效性、采用、实现和维护)框架。对包括项目参与者和实施者在内的39名关键线人进行了深入的半结构化访谈。该计划达到了目标群体的59%。设计和实施以集体和关系繁荣的土著哲学为基础。通过参与,个人加强了联系,建立了信任关系。讲故事和讲故事使参与者能够将自己定位在一个正在进行的故事中,这个故事描绘了他们的家庭和社区历史。愿望与计划目标一致的学校采纳了该计划,尽管实施受到COVID-19限制的阻碍。该计划运用了对基于优势的实践,关系以及抵抗和恢复的作用的复杂理解来满足参与者的需求。该评估提供了支持该计划有效性的证据,并突出了促成其成功的因素。研究结果强调,针对城市环境中年轻女性的有效项目将与文化和身份的联系作为其核心。它说明了土著社区控制的服务提供的价值。在实施或资助类似的项目时,应该有两个主要的见解来指导决策。首先,必须把重点放在文化的连续性和赋权上。其次,成功取决于消除实际障碍,并通过肯定、有趣和鼓舞人心的互动吸引参与者。在整个研究和写作过程中,土著合作者的领导能力和知识是进行严格和相关评估的关键。
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引用次数: 0
Navigating care through connection: How patient navigators strengthen the care experiences of Aboriginal and Torres Strait Islander peoples living with kidney failure 通过连接导航护理:病人导航员如何加强土著和托雷斯海峡岛民生活在肾衰竭的护理经验
Pub Date : 2025-12-23 DOI: 10.1016/j.fnhli.2025.100101
Matilda D’Antoine (Paakantyi) , Isabelle Haklar , Madison Cachagee (Mushkegowuk) , Katie Cundale , Samantha Bateman , Stephen McDonald , Janet Kelly , Kim O’Donnell (Malyangapa, Barkindji) , Shilpanjali Jesudason , Isaac Brown (Yuin) , Kynesha Temple (Ngarrindjeri, Narungga) , Jampitjinpa Ross (Walpiri) , David Croker (Anmatjere, Walpiri, Jingili) , Neil Wilkshire (Warrumangu, Luritja) , Peter Henwood (Muk Muk Maranrunggu) , Cedrina Algy (Gurrindji) , Rhanee Lester (Adnyamathanha) , Kate Tyrell , Heather Hall , Michelle Misener , Kelli Owen (Kaurna, Narungga and Ngarrindjeri)

Purpose

Evidence suggests that patient navigators (PNs) can improve patient engagement, emotional wellbeing and clinical outcomes. This study explored how PNs influence the care experiences of Aboriginal and Torres Strait Islander peoples living with kidney failure, from the perspectives of patients and health service staff.

Methods

Qualitative data were collected through kidney journey mapping and yarning interviews across four kidney health services employing PNs in the Northern Territory and South Australia. Data were thematically analysed to understand patient care experiences with and without PN support.

Main findings

Patients reported challenges around inadequate communication, difficulty accessing appropriate services and support, poor cultural safety, and the emotional toll of treatment. Support included family and patient networks, positive relationships with health staff, and holistic models of care. PNs played a supportive role by sharing their kidney journey experiences, providing cultural connection, peer support and bridging systemic gaps.

Principle conclusions

PNs strengthened patient care experiences by addressing service gaps, improving cultural support and sharing from lived experience. Embedding PNs into standard kidney care is a critical step toward achieving culturally safe, equitable and responsive health systems.
目的:有证据表明,患者导航员(PNs)可以提高患者的参与度、情绪健康和临床结果。本研究从患者和卫生服务人员的角度探讨了主治医生如何影响土著和托雷斯海峡岛民肾衰竭患者的护理经验。方法通过在北领地和南澳大利亚聘用执业护士的四家肾脏健康服务机构进行肾脏旅程测绘和访谈,收集定性数据。对数据进行主题分析,以了解有和没有PN支持的患者护理经验。患者报告的挑战包括沟通不足、难以获得适当的服务和支持、文化安全性差以及治疗造成的情感损失。支持包括家庭和病人网络、与卫生工作人员的积极关系以及整体护理模式。PNs通过分享他们的肾脏旅程经验,提供文化联系,同伴支持和弥合系统差距发挥了支持作用。主要结论:spns通过解决服务差距、改善文化支持和分享生活经验来加强患者护理体验。将PNs纳入标准肾脏护理是实现文化上安全、公平和反应灵敏的卫生系统的关键一步。
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引用次数: 0
Aboriginal community researchers: A short report on the research training program and research experience with the Virtual Rural Generalist Service evaluation 原住民社区研究人员:关于虚拟乡村通才服务评估之研究训练计划与研究经验之简短报告
Pub Date : 2025-12-19 DOI: 10.1016/j.fnhli.2025.100102
Anna Thompson , Andrew Carroll (Gamilaraay) , Deborah Kenna OAM (Gamilaraay) , Elizabeth Kennedy-Williams (Gamilaroi) , Shirley-Ann Merritt (Wiradjuri) , John Skinner , Carmen Parter (Murri) , Cara Cross (Worimi and Biripai) , Georgina M. Luscombe , Emily Saurman
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引用次数: 0
Racism and cultural safety for Indigenous general practice trainees: An exploratory study of how to support training, careers and professional wellbeing 种族主义和土著全科实习学员的文化安全:如何支持培训、职业和职业福利的探索性研究
Pub Date : 2025-01-01 DOI: 10.1016/j.fnhli.2024.100038
Talila Milroy (Yindjibarndi and Palyku), Jacqueline Frayne

Purpose

Racism as a social determinant of health has known impacts on the physical and mental health of Indigenous peoples, which extends to Indigenous doctors in training and is a barrier to the growth of the Indigenous health workforce in Australia. This study aimed to explore racism and cultural safety within the professional experiences of Australian Indigenous general practice (GP) trainees, to elucidate barriers and facilitators to their training, careers and professional wellbeing.

Methods

A sequential exploratory mixed methods study was conducted in 2020 and 2021 through an initial quantitative online administered questionnaire followed by qualitative semi-structured interviews with Indigenous GP registrars, from either metropolitan or rural areas, undertaking GP training in Australia. The main outcome measures included online responses to the Measure of Indigenous Racism Experiences (MIRE) questionnaire, which measures several dimensions of racism, and data from thematic analysis of semi-structured interviews undertaken following the online questionnaire.

Main findings

The MIRE questionnaire responses revealed experiences of racism across multiple levels. These findings were integrated and expanded with the central themes drawn from the interviews. Themes focused on GP training and training environments and operated across interactions with peers, supervisors and patients. The identified themes were i) cultural identity, with the subthemes of professional wellbeing and professional goals and identity; ii) training challenges, including racism and career development; and iii) training facilitators, including specific support and mentorship.

Principal conclusions

Australian Indigenous GP trainees value their cultural identity in relation to their professional goals and wellbeing. However, challenges for trainees centre around the lack of cultural safety and presence of racism, which is pervasive across their professional life. Strategies to address this could include further provision of specific support, specific culturally safe training placements, networking and mentorship.
目的种族主义作为健康的一个社会决定因素,对土著人民的身心健康产生了众所周知的影响,这种影响延伸到正在接受培训的土著医生,并阻碍了澳大利亚土著保健人员队伍的发展。本研究旨在探讨种族主义和文化安全在澳大利亚土著全科医生(GP)学员的专业经验,阐明障碍和促进他们的培训,职业生涯和职业福利。方法在2020年和2021年进行了一项顺序探索性混合方法研究,通过最初的定量在线管理问卷,然后对在澳大利亚接受全科医生培训的来自大都市或农村地区的土著全科医生注册者进行定性半结构化访谈。主要结果测量包括对土著种族主义经历测量(MIRE)问卷的在线回答,该问卷测量种族主义的几个维度,以及在线问卷调查后进行的半结构化访谈的主题分析数据。主要发现:MIRE问卷的回答揭示了不同层次的种族主义经历。这些发现与从访谈中得出的中心主题进行了整合和扩展。主题集中在全科医生培训和培训环境,并通过与同行、主管和患者的互动进行操作。确定的主题是:(1)文化认同,副主题是职业幸福和职业目标与认同;Ii)培训挑战,包括种族主义和职业发展;培训辅导员,包括具体的支持和指导。澳大利亚土著全科医生学员将他们的文化认同与他们的职业目标和幸福联系起来。然而,学员面临的挑战集中在缺乏文化安全和种族主义的存在,这在他们的职业生涯中无处不在。解决这一问题的战略可包括进一步提供具体支持、具体的文化安全培训安排、网络和指导。
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引用次数: 0
Measuring resilience using Strong Souls in the Longitudinal Study of Indigenous Children: Evaluating psychometric properties using a Rasch measurement approach 在土著儿童的纵向研究中使用强大的灵魂测量弹性:使用Rasch测量方法评估心理测量特性
Pub Date : 2025-01-01 DOI: 10.1016/j.fnhli.2024.100037
Ella Gorman , Roz Walker , Helen Davis , Carrington C.J. Shepherd , Rhonda Marriott (Nyikina)

Purpose

Rigorously evaluated psychometric instruments are necessary to measure constructs relevant to wellbeing, such as resilience. The availability of high-quality instruments for use with Aboriginal young people in Australia is growing but remains limited. This study used data from the Longitudinal Study of Indigenous Children (LSIC) to psychometrically evaluate the Resilience subscale from the social and emotional wellbeing (SEWB) instrument, Strong Souls, for a nationwide sample of Aboriginal adolescents, using alternative psychometric methods to previous research.

Methods

Using a Rasch measurement approach, cross-sectional data from Wave 9 of LSIC were used to ascertain the psychometric properties of the Resilience subscale from Strong Souls. Using the responses from 516 Aboriginal young people (age 11.5 to 13 years) to the 12-item scale, Rasch techniques were applied to determine item independence, response category adequacy, differential item functioning (DIF), person and item reliability, item fit and unidimensionality. Two versions of the instrument were evaluated: the full 12-item version, as completed by participants, and an 8-item version, as recommended for use by previous research based on different psychometric methods.

Main findings

Both versions of the instrument met several Rasch model requirements for reliable measurement, including demonstrations of unidimensionality (first off factor construct < 2), item independence (all items Q3∗ < 0.30), and item fit statistics within an acceptable range (0.60 < X < 1.40). However, both instrument versions displayed less adequate person separation (PSI) and reliability (PRI) statistics (12-item scale: PSI = 1.18, PRI = 0.58; 8-item scale: PSI = 0.71, PRI = 0.33).

Principal conclusions

Using a Rasch measurement approach to psychometrically evaluate the Strong Souls Resilience subscale in a sample of Aboriginal young people from LSIC, this study provided novel evidence of the functioning of this popular instrument from an alternative psychometric perspective. With mixed results regarding meeting Rasch recommendations, these findings provide a strong evidence base for psychometric strengths as well as opportunities to improve the robustness of this instrument, and ultimately offer a tool that can more accurately inform services, policy and practice to effectively support resilience and wellbeing in Aboriginal young people.
目的严格评估的心理测量工具对于测量与健康相关的结构是必要的,例如弹性。在澳大利亚,供土著青年使用的高质量乐器越来越多,但仍然有限。本研究使用土著儿童纵向研究(LSIC)的数据,采用替代以往研究的心理测量方法,对全国土著青少年样本的社会和情感健康(SEWB)工具(Strong Souls)中的弹性子量表进行心理测量学评估。方法采用Rasch测量法,利用LSIC第9波的横断面数据,确定《坚强灵魂》弹性分量表的心理测量特性。本研究以516名11.5 ~ 13岁原住民青年为研究对象,采用Rasch技术测定问卷的项目独立性、反应类别充分性、差异项目功能、人与项目信度、项目契合度和单维性。评估了两个版本的工具:完整的12项版本,由参与者完成,以及8项版本,根据不同的心理测量方法推荐使用的先前研究。主要发现:仪器的两个版本都满足可靠测量的几个拉希模型要求,包括单维性的证明(第一因子结构);2)、项目独立性(所有项目Q3 * <;0.30),项目拟合统计在可接受范围内(0.60 <;X & lt;1.40)。然而,两种版本的仪器显示较不充分的人员分离(PSI)和可靠性(PRI)统计(12项量表:PSI = 1.18, PRI = 0.58;8项量表:PSI = 0.71, PRI = 0.33)。本研究采用Rasch测量方法对来自LSIC的土著青年样本进行心理测量,从另一个心理测量角度为这一流行工具的功能提供了新的证据。虽然在满足Rasch建议方面的结果好坏兼有,但这些发现为心理测量学的优势提供了强有力的证据基础,也为提高该工具的稳健性提供了机会,并最终提供了一种工具,可以更准确地为服务、政策和实践提供信息,以有效地支持土著年轻人的恢复力和福祉。
{"title":"Measuring resilience using Strong Souls in the Longitudinal Study of Indigenous Children: Evaluating psychometric properties using a Rasch measurement approach","authors":"Ella Gorman ,&nbsp;Roz Walker ,&nbsp;Helen Davis ,&nbsp;Carrington C.J. Shepherd ,&nbsp;Rhonda Marriott (Nyikina)","doi":"10.1016/j.fnhli.2024.100037","DOIUrl":"10.1016/j.fnhli.2024.100037","url":null,"abstract":"<div><h3>Purpose</h3><div>Rigorously evaluated psychometric instruments are necessary to measure constructs relevant to wellbeing, such as resilience. The availability of high-quality instruments for use with Aboriginal young people in Australia is growing but remains limited. This study used data from the Longitudinal Study of Indigenous Children (LSIC) to psychometrically evaluate the Resilience subscale from the social and emotional wellbeing (SEWB) instrument, Strong Souls, for a nationwide sample of Aboriginal adolescents, using alternative psychometric methods to previous research.</div></div><div><h3>Methods</h3><div>Using a Rasch measurement approach, cross-sectional data from Wave 9 of LSIC were used to ascertain the psychometric properties of the Resilience subscale from Strong Souls. Using the responses from 516 Aboriginal young people (age 11.5 to 13 years) to the 12-item scale, Rasch techniques were applied to determine item independence, response category adequacy, differential item functioning (DIF), person and item reliability, item fit and unidimensionality. Two versions of the instrument were evaluated: the full 12-item version, as completed by participants, and an 8-item version, as recommended for use by previous research based on different psychometric methods.</div></div><div><h3>Main findings</h3><div>Both versions of the instrument met several Rasch model requirements for reliable measurement, including demonstrations of unidimensionality (first off factor construct &lt; 2), item independence (all items Q<sub>3∗</sub> &lt; 0.30), and item fit statistics within an acceptable range (0.60 &lt; X &lt; 1.40). However, both instrument versions displayed less adequate person separation (PSI) and reliability (PRI) statistics (12-item scale: PSI = 1.18, PRI = 0.58; 8-item scale: PSI = 0.71, PRI = 0.33).</div></div><div><h3>Principal conclusions</h3><div>Using a Rasch measurement approach to psychometrically evaluate the Strong Souls Resilience subscale in a sample of Aboriginal young people from LSIC, this study provided novel evidence of the functioning of this popular instrument from an alternative psychometric perspective. With mixed results regarding meeting Rasch recommendations, these findings provide a strong evidence base for psychometric strengths as well as opportunities to improve the robustness of this instrument, and ultimately offer a tool that can more accurately inform services, policy and practice to effectively support resilience and wellbeing in Aboriginal young people.</div></div>","PeriodicalId":100532,"journal":{"name":"First Nations Health and Wellbeing - The Lowitja Journal","volume":"3 ","pages":"Article 100037"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143487465","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
What about the soles: We need the primary data in Aboriginal and Torres Strait Islander foot health to ‘Close the Gap’ 鞋底呢?我们需要土著人和托雷斯海峡岛民足部健康的原始数据来“缩小差距”。
Pub Date : 2025-01-01 DOI: 10.1016/j.fnhli.2024.100041
James A. Charles (Kaurna) , Elizabeth Tiernan , Sara Jones
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引用次数: 0
These mob here have integrity; they genuinely care about the people: Service users’ and care providers’ perspectives on enablers of good chronic disease care for Aboriginal and Torres Strait Islander peoples 这里的暴徒很正直;他们真正关心人民:服务使用者和护理提供者对土著和托雷斯海峡岛民良好慢性病护理的促进因素的看法
Pub Date : 2025-01-01 DOI: 10.1016/j.fnhli.2025.100063
Sarah Catherine Bourke (Gamilaroi, Jaru, Gidja) , Deborah Wong , Uday Narayan Yadav , Andrea Timothy , Chelsea Liu , Abby-Rose Cox (Kija, Nimanburru) , Rosemary Wyber
Research about Aboriginal and Torres Strait Islander chronic disease management in primary healthcare services rarely considers the perspectives of service users in identifying what works. This research aimed to elevate the voices of clients and providers from high performing primary healthcare services (termed Lighthouse Services) around Australia about the successes and opportunities for improvement in chronic disease management for Aboriginal and Torres Strait Islander peoples. Seventy-five individuals, representing clients (n = 29), their carers (n = 7) and health providers (n = 39), from four Lighthouse Services participated in in-depth focus groups and interviews conducted by the researchers and local partners. The transcripts of these discussions were reviewed in NVivo 14 (https://lumivero.com/products/nvivo/) using reflexive thematic analysis to identify key themes representing their lived experiences.
Access, Communication, Systems, Hub and spokes, Relationships and Workforce were the six themes chosen to represent the range of personal experiences about what works for managing chronic disease at the primary healthcare level. Services that effectively employed a holistic patient-centred model of care, provided culturally safe spaces and were connected to and involved in the community were viewed as providing good care for their clients. The findings of this study support existing literature and make an important new contribution by focusing on the insights of clients, carers and service providers about what and why different aspects of chronic disease care work. It is suggested that this research approach would be beneficial across a range of other settings (e.g. non-Aboriginal community-controlled health organisations and urban services) and conditions (e.g. acute care, social and emotional wellbeing) to enhance Aboriginal and Torres Strait Islander health outcomes.
关于初级保健服务中土著和托雷斯海峡岛民慢性病管理的研究很少考虑到服务使用者的观点,以确定有效的方法。这项研究旨在提高澳大利亚各地高绩效初级保健服务(称为灯塔服务)的客户和提供者的声音,使他们了解改善土著和托雷斯海峡岛民慢性病管理的成功和机会。来自四个灯塔服务机构的75名代表客户(n = 29)、他们的照顾者(n = 7)和保健提供者(n = 39)的个人参加了由研究人员和当地合作伙伴进行的深入焦点小组和访谈。在NVivo 14 (https://lumivero.com/products/nvivo/)中回顾了这些讨论的文本,使用反身性主题分析来确定代表他们生活经历的关键主题。访问、通信、系统、中心和辐条、关系和劳动力是所选择的六个主题,代表了在初级卫生保健一级管理慢性病的个人经验范围。有效地采用以病人为中心的整体护理模式,提供文化安全空间,并与社区联系和参与的服务被视为为其客户提供良好的护理。本研究的发现支持了现有文献,并通过关注客户,护理人员和服务提供者对慢性病护理不同方面的作用和原因的见解,做出了重要的新贡献。建议这种研究方法将在一系列其他环境(例如非土著社区控制的卫生组织和城市服务)和条件(例如急症护理、社会和情感健康)中有益,以提高土著和托雷斯海峡岛民的健康结果。
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引用次数: 0
First Nations parents’ experiences of COVID-19 and associations with symptoms of complex post-traumatic stress disorder 第一民族父母的COVID-19经历及其与复杂创伤后应激障碍症状的关联
Pub Date : 2025-01-01 DOI: 10.1016/j.fnhli.2025.100086
Christina L. Heris , Taylor Glover (Dharawal) , Tess Bright , Simon Graham (Narungga) , Shannon K. Bennetts , Kimberley A. Jones , Michelle Kennedy (Wiradjuri) , Caroline Atkinson (Bundjalung) , Catherine Chamberlain (Trawlwoolway)

Purpose

To examine associations between First Nations parents’ experiences during the COVID-19 pandemic and symptoms of complex post-traumatic stress disorder (C-PTSD).

Methods

First Nations parents (n = 110) completed a 90-minute telephone interview between October 2021 and July 2022. Parents self-reported their PTSD or C-PTSD symptoms using the International Trauma Questionnaire (categorised as no/low vs. high levels), COVID-19 events (e.g. testing, diagnosis, isolation) and perceived socioemotional changes in life situation (e.g. quality of relationships) compared with before the pandemic. Logistic regression analysed associations between C/PTSD symptoms (outcome) and demographic factors, COVID-19 events, perceived socioemotional changes since COVID-19 (exposures).

Main findings

More than a quarter (27%) of parents reported high levels of C-PTSD/PTSD symptoms. Most (90%) reported at least one COVID-19 event. Parents who had experienced worsening racism and inequality since the pandemic (OR 0.29, 95% CI 0.11–0.79) or held a Health Care Card (OR 0.27, 95% CI 0.10–0.74) were significantly less likely to report no/low levels of C-PTSD/PTSD symptoms.

Principal conclusions

Financial stress, racism and inequality were associated with increased trauma symptoms, highlighting the importance of implementing trauma-informed public health emergency responses during a pandemic. Those who had fewer disruptions to cultural practices were more likely to be resilient to the stressors of the pandemic, reinforcing the need for a culturally-responsive, trauma-informed public health emergency framework for First Nations communities. Emergency responses that address these factors while optimising safe opportunities to maintain cultural obligations and social connection are essential.
目的研究新冠肺炎大流行期间原住民父母的经历与复杂创伤后应激障碍(C-PTSD)症状之间的关系。方法:在2021年10月至2022年7月期间,110名原住民父母完成了90分钟的电话访谈。父母使用国际创伤问卷(分类为无/低水平与高水平)、COVID-19事件(如检测、诊断、隔离)以及与大流行前相比,生活状况中感知到的社会情绪变化(如关系质量)自我报告其创伤后应激障碍或C-PTSD症状。Logistic回归分析了C/PTSD症状(结果)与人口因素、COVID-19事件、自COVID-19以来感知的社会情绪变化(暴露)之间的关联。主要发现:超过四分之一(27%)的父母报告有高水平的C-PTSD/PTSD症状。大多数(90%)报告了至少一次COVID-19事件。自大流行以来经历过日益恶化的种族主义和不平等(OR 0.29, 95% CI 0.11-0.79)或持有医疗保健卡(OR 0.27, 95% CI 0.10-0.74)的父母报告无/低水平的C-PTSD/PTSD症状的可能性显着降低。主要结论:经济压力、种族主义和不平等与创伤症状的增加有关,突出了在大流行期间实施创伤知情的公共卫生应急反应的重要性。那些文化习俗受到干扰较少的人更有可能抵御大流行病的压力,因此更有必要为第一民族社区建立一个对文化有反应的、了解创伤的公共卫生应急框架。必须采取应急措施,解决这些因素,同时尽量利用安全机会保持文化义务和社会联系。
{"title":"First Nations parents’ experiences of COVID-19 and associations with symptoms of complex post-traumatic stress disorder","authors":"Christina L. Heris ,&nbsp;Taylor Glover (Dharawal) ,&nbsp;Tess Bright ,&nbsp;Simon Graham (Narungga) ,&nbsp;Shannon K. Bennetts ,&nbsp;Kimberley A. Jones ,&nbsp;Michelle Kennedy (Wiradjuri) ,&nbsp;Caroline Atkinson (Bundjalung) ,&nbsp;Catherine Chamberlain (Trawlwoolway)","doi":"10.1016/j.fnhli.2025.100086","DOIUrl":"10.1016/j.fnhli.2025.100086","url":null,"abstract":"<div><h3>Purpose</h3><div>To examine associations between First Nations parents’ experiences during the COVID-19 pandemic and symptoms of complex post-traumatic stress disorder (C-PTSD).</div></div><div><h3>Methods</h3><div>First Nations parents (<em>n</em> = 110) completed a 90-minute telephone interview between October 2021 and July 2022. Parents self-reported their PTSD or C-PTSD symptoms using the International Trauma Questionnaire (categorised as no/low vs. high levels), COVID-19 events (e.g. testing, diagnosis, isolation) and perceived socioemotional changes in life situation (e.g. quality of relationships) compared with before the pandemic. Logistic regression analysed associations between C/PTSD symptoms (outcome) and demographic factors, COVID-19 events, perceived socioemotional changes since COVID-19 (exposures).</div></div><div><h3>Main findings</h3><div>More than a quarter (27%) of parents reported high levels of C-PTSD/PTSD symptoms. Most (90%) reported at least one COVID-19 event. Parents who had experienced worsening racism and inequality since the pandemic (OR 0.29, 95% CI 0.11–0.79) or held a Health Care Card (OR 0.27, 95% CI 0.10–0.74) were significantly less likely to report no/low levels of C-PTSD/PTSD symptoms.</div></div><div><h3>Principal conclusions</h3><div>Financial stress, racism and inequality were associated with increased trauma symptoms, highlighting the importance of implementing trauma-informed public health emergency responses during a pandemic. Those who had fewer disruptions to cultural practices were more likely to be resilient to the stressors of the pandemic, reinforcing the need for a culturally-responsive, trauma-informed public health emergency framework for First Nations communities. Emergency responses that address these factors while optimising safe opportunities to maintain cultural obligations and social connection are essential.</div></div>","PeriodicalId":100532,"journal":{"name":"First Nations Health and Wellbeing - The Lowitja Journal","volume":"3 ","pages":"Article 100086"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145519261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Community acceptability of lowering the eligibility age of government funded bowel screening for Aboriginal South Australians to 40 years 将政府资助的南澳大利亚土著居民肠道筛查的资格年龄降低到40岁的社区可接受性
Pub Date : 2025-01-01 DOI: 10.1016/j.fnhli.2025.100045
Karla J. Canuto (Naghir Tribe of the Kulkalgul Clan) , Eugene Warrior (Wirangu, Bungala, Kokatha and Antakerinya) , Sharon Clarke (Wergaia, Wemba Wemba, Djadwajali and Gunditjmara) , Nathan Rigney (Ngarrindjeri) , Jie-Bin Lew , Eleonora Feletto , Katina D’Onise

Purpose

Building on a study that found that lowering the age of bowel screening for Aboriginal and Torres Strait Islander peoples to 40 years would be cost-effective, this research examined the acceptability of lowering the bowel screening age for Aboriginal and Torres Strait Islander peoples in South Australia.

Methods

Aboriginal community members aged < 50 years were recruited to form Aboriginal men’s (16 men) and women’s (nine women) bowel cancer screening councils. The councils were presented with detailed information relating to the topic and deliberated over two days.

Main findings

The men’s and women’s councils were unanimous in their support for reducing the age of bowel screening for Aboriginal and Torres Strait Islander peoples. The councils identified barriers to reducing the age at participation, and participation in screening in general. Both councils were highly engaged in the process of the two-day deliberation.

Principal conclusions

Lowering the age range for Aboriginal and Torres Strait Islander peoples participating in the bowel screening program to 40 years was acceptable to both Aboriginal bowel cancer screening councils.
目的:在一项研究发现将土著和托雷斯海峡岛民的肠道筛查年龄降低到40岁具有成本效益的基础上,本研究考察了降低南澳大利亚土著和托雷斯海峡岛民肠道筛查年龄的可接受性。方法:选取年龄在<;50岁的人被招募成立土著男性(16名男性)和女性(9名女性)肠癌筛查委员会。向各理事会提交了有关该专题的详细资料,并进行了两天的审议。主要发现男性和女性委员会一致支持降低原住民和托雷斯海峡岛民的肠道检查年龄。理事会确定了降低参与年龄和一般参与筛查的障碍。两个委员会都高度参与了为期两天的审议过程。主要结论将土著居民和托雷斯海峡岛民参加肠道筛查项目的年龄范围降低到40岁是两个土著肠癌筛查委员会都可以接受的。
{"title":"Community acceptability of lowering the eligibility age of government funded bowel screening for Aboriginal South Australians to 40 years","authors":"Karla J. Canuto (Naghir Tribe of the Kulkalgul Clan) ,&nbsp;Eugene Warrior (Wirangu, Bungala, Kokatha and Antakerinya) ,&nbsp;Sharon Clarke (Wergaia, Wemba Wemba, Djadwajali and Gunditjmara) ,&nbsp;Nathan Rigney (Ngarrindjeri) ,&nbsp;Jie-Bin Lew ,&nbsp;Eleonora Feletto ,&nbsp;Katina D’Onise","doi":"10.1016/j.fnhli.2025.100045","DOIUrl":"10.1016/j.fnhli.2025.100045","url":null,"abstract":"<div><h3>Purpose</h3><div>Building on a study that found that lowering the age of bowel screening for Aboriginal and Torres Strait Islander peoples to 40 years would be cost-effective, this research examined the acceptability of lowering the bowel screening age for Aboriginal and Torres Strait Islander peoples in South Australia.</div></div><div><h3>Methods</h3><div>Aboriginal community members aged &lt; 50 years were recruited to form Aboriginal men’s (16 men) and women’s (nine women) bowel cancer screening councils. The councils were presented with detailed information relating to the topic and deliberated over two days.</div></div><div><h3>Main findings</h3><div>The men’s and women’s councils were unanimous in their support for reducing the age of bowel screening for Aboriginal and Torres Strait Islander peoples. The councils identified barriers to reducing the age at participation, and participation in screening in general. Both councils were highly engaged in the process of the two-day deliberation.</div></div><div><h3>Principal conclusions</h3><div>Lowering the age range for Aboriginal and Torres Strait Islander peoples participating in the bowel screening program to 40 years was acceptable to both Aboriginal bowel cancer screening councils.</div></div>","PeriodicalId":100532,"journal":{"name":"First Nations Health and Wellbeing - The Lowitja Journal","volume":"3 ","pages":"Article 100045"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143684277","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mapping Aboriginal children’s social and emotional wellbeing: Development and validation of a new tool in an Aboriginal cohort study 绘制土著儿童的社会和情感健康:在土著队列研究中一个新工具的开发和验证
Pub Date : 2025-01-01 DOI: 10.1016/j.fnhli.2025.100062
Arwen Nikolof , Deirdre Gartland , Karen Glover , Cathy Leane , Rohan Carmody , Heather Carter , Stephanie J. Brown , Yvonne Clark

Purpose

This study aimed to develop the first Aboriginal-led co-designed tool to map Australian Aboriginal children’s social and emotional wellbeing (SEWB) based on holistic definitions of wellbeing that have been discussed, supported and refined by Aboriginal and Torres Strait Islander peoples over the last 30 years.

Methods

Development of the Aboriginal Children’s SEWB Tool was embedded in wave 2 follow-up of an existing cohort of families: the Aboriginal Families Study (AFS). Items from a questionnaire completed by mothers/caregivers of the study children (aged 5–8 years) were selected to map the seven domains of the SEWB framework. The process was Aboriginal-led by the first author, the AFS research team and Aboriginal Governance Group. Psychometric testing and revision included assessment of the structure, testing of the internal consistency of domains, and criterion validity against the Strengths and Difficulties Questionnaire (SDQ).

Main findings

The Aboriginal Children’s SEWB Tool (parent/caregiver report) comprises 80 items grouped into 29 indicators across six domains: Body; Mind and emotion; Family and kinship; Community; Culture; and Country, spirit and spirituality. Criterion validity was supported: children with high scores on the SEWB Tool had seven times higher odds of positive emotional wellbeing and four times the odds of high mental health competence, as measured with the SDQ, compared with children with low scores (Adj. OR 7.7, 95% CI 2.5 – 23.9 and Adj. OR 3.9, 95% CI 1.4 – 10.2, respectively). Fewer items were available on connection to Country, spirit, spirituality and ancestors; further refinement in these areas will be of benefit.

Principal conclusion

The Aboriginal Children’s SEWB Tool was developed in response to a lack of measures recognising Aboriginal and Torres Strait Islander peoples’ conceptualisations of child social and emotional wellbeing. The new tool provides a holistic picture of SEWB experienced by Aboriginal children, with the capacity to map strengths, gaps and areas for healing across body, mind and emotion, family and kinship, community, culture and Country, spirit and spirituality. Use of the tool would support health and social practitioners working with individual children and families, within schools as well as in research settings. Work is needed to further enhance the tool.
本研究旨在开发首个由原住民主导的共同设计工具,以绘制澳大利亚原住民儿童的社会和情感健康(SEWB),该工具基于过去30年来原住民和托雷斯海峡岛民讨论、支持和完善的整体健康定义。方法原住民儿童SEWB工具的开发嵌入到现有家庭队列的第二波随访中:原住民家庭研究(AFS)。从研究儿童(5-8岁)的母亲/照顾者完成的问卷中选择项目来绘制SEWB框架的七个领域。这个过程是由第一作者、AFS研究小组和土著治理小组领导的。心理测量测试和修订包括结构评估、领域内部一致性测试和针对优势与困难问卷(SDQ)的效度。土著儿童SEWB工具(父母/照顾者报告)包括80个项目,分为6个领域的29个指标:身体;思想和情感;家庭和亲属关系;社区;文化;国家、精神和灵性。标准效度得到支持:用SDQ测量,SEWB工具得分高的儿童与得分低的儿童相比,积极情绪健康的几率高7倍,高心理健康能力的几率高4倍(分别为Adj. OR 7.7, 95% CI 2.5 - 23.9和Adj. OR 3.9, 95% CI 1.4 - 10.2)。与国家、精神、灵性和祖先的联系较少;在这些方面的进一步改进将是有益的。原住民儿童社会与情感健康工具是针对原住民和托雷斯海峡岛民对儿童社会和情感健康概念缺乏认可的措施而开发的。新工具提供了土著儿童所经历的SEWB的整体情况,能够绘制出身体、思想和情感、家庭和亲属关系、社区、文化和国家、精神和灵性方面的优势、差距和治疗领域。该工具的使用将支持卫生和社会从业人员在学校和研究环境中与个别儿童和家庭开展工作。需要进一步改进该工具。
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First Nations Health and Wellbeing - The Lowitja Journal
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