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Involving older adults and unpaid carers in the research cycle: reflections on implementing the UK national standards for public involvement into practice 让老年人和无酬照护者参与研究周期:关于将英国公众参与国家标准付诸实践的思考
IF 1.5 Q2 Nursing Pub Date : 2023-12-26 DOI: 10.1108/qaoa-03-2023-0019
Catrin Hedd Jones, Diane Seddon, Katherine Algar-Skaife, Carol Maddock, Stephanie Green
Purpose This paper aims to share how the Centre for Ageing and Dementia Research co-designs research within a national programme of work to improve the lives of older adults and those affected by dementia. Through examples of this work, the authors identify the barriers and enablers to participatory approaches and lessons to inform future involvement activities. Design/methodology/approach This study reflects on implementing the UK National Standards for Public Involvement into practice. Of international relevance, the observations span the research process from research prioritisation and design to research implementation and knowledge exchange. Findings This study demonstrates the importance of using a relational approach, working toward a common purpose and engaging in meaningful dialogue. Only through offering choice and flexibility and actively learning from one another can co-design lead to synergistic relationships that benefit everyone. Research limitations/implications Key implications for researchers engaged in patient and public involvement are be receptive to other people’s views and acknowledge expertise of those with lived experience alongside those with academic expertise. Training, resources and time are required to effectively support involvement and meaningful relationships. A nominated contact person enables trust and mutual understanding to develop. This is an ongoing collective learning experience that should be embedded throughout the entire research process. Originality/value This paper demonstrates how the standards are implemented with people who are often excluded from research to influence a national programme of work.
目的 本文旨在分享老龄化与痴呆症研究中心如何在国家工作计划内共同设计研究,以改善老年人和痴呆症患者的生活。通过这项工作的实例,作者指出了参与式方法的障碍和有利因素,并总结了经验教训,为今后的参与活动提供参考。 设计/方法/途径 本研究反映了英国公众参与国家标准在实践中的实施情况。从研究的优先次序和设计到研究的实施和知识交流,研究过程中的观察具有国际意义。 研究结果 这项研究表明了采用关系方法、为共同目标而努力以及开展有意义对话的重要性。只有通过提供选择和灵活性并积极相互学习,共同设计才能产生协同关系,使每个人受益。 研究局限性/启示 对参与患者和公众参与的研究人员的主要启示是,要善于接受他人的意见,并承认具有生活经验的人和具有学术专长的人的专业知识。需要培训、资源和时间来有效支持参与和建立有意义的关系。指定联络人可以促进信任和相互理解。这是一种持续的集体学习体验,应贯穿整个研究过程。 原创性/价值 本文展示了如何与经常被排除在研究之外的人员一起实施标准,以影响国家工作计划。
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引用次数: 0
Participatory action research and empowerment of nursing home residents 参与式行动研究和增强养老院居民的能力
IF 1.5 Q2 Nursing Pub Date : 2023-12-19 DOI: 10.1108/qaoa-08-2023-0053
Annette Bilfeldt, Marianne Mahler
PurposeThe purpose of this paper is to discuss participatory action research with staff, residents and relatives contributed to the residents’ quality of life through the development of an inclusive praxis in a public nursing home in Denmark. The project addressed the residents’ reports about a lack of influence in their everyday lives.Design/methodology/approachThe project used future-creating workshops as an important methodological tool. Theoretical concepts about developing a social reflexive and colletive morally obliging praxis were central to frame democratic learning and acting. The theoretical concepts of empowerment and capability were also applied. This paper will outline the methods and the results obtained.FindingsLearning processes were initiated, enabling staff to respectfully engage in dialogue with residents and their relatives about their needs and wishes. The development of a democratic knowledge-building process was established based on the perspectives of the residents, relatives and staff. In conclusion, the project contributed to the development of a more reflective and democratic praxis focused on empowering the residents as the primary “stakeholders” in the daily life of the nursing home.Originality/valueThe research paper is based on the authors’ own research.
本文旨在讨论丹麦一家公立疗养院通过发展包容性实践,与员工、居民和亲属共同开展的参与式行动研究对提高居民生活质量的贡献。设计/方法/途径该项目将未来创造研讨会作为一种重要的方法论工具。关于发展社会反思和共同道德义务实践的理论概念,是构建民主学习和行动的核心。此外,还运用了赋权和能力的理论概念。本文将概述所采用的方法和所取得的成果。研究结果启动了学习过程,使工作人员能够以尊重的态度与住户及其亲属就他们的需求和愿望进行对话。根据住户、亲属和工作人员的观点,建立了一个民主的知识积累过程。总之,该项目促进了更具反思性和民主性的实践的发展,其重点是在养老院的日常生活中赋予作为主要 "利益相关者 "的院友权力。
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引用次数: 0
The relationship between older adults’ perceptions of ageing and depression: a systematic review 老年人对老龄化的认知与抑郁之间的关系:系统性综述
IF 1.5 Q2 Nursing Pub Date : 2023-12-19 DOI: 10.1108/qaoa-07-2022-0044
Gemma Hartley, Jack Purrington
PurposePerceptions of ageing towards the self and towards others can positively and negatively impact an older adult’s mental wellbeing. This paper aims to consolidate literature examining the relationship between perceptions of ageing and depression in older adults to inform both practice and policy for older adult mental health services.Design/methodology/approachQuantitative research articles examining perceptions of ageing and depression in older adults were identified through searches on three electronical databases, alongside forward and backwards citation searches. A total of 14 articles involving 31,211 participants were identified.FindingsGreater negative attitudes towards ageing were associated with higher levels of depressive symptoms and greater positive attitudes towards ageing were associated with lower levels of depressive symptoms or higher levels of happiness. However, the causal direction of this relationship could not be determined. Studies demonstrated that perceptions of ageing also act as a moderator in the relationship between depression and health status, hopelessness and personality traits. Future research should attempt to examine the relationship between perceptions of ageing and depression in older adults to attempt to identify the causal direction of this relationship.Originality/valueThis is the only systematic review the authors are aware of consolidating literature which explores the relationship between older adults’ perceptions of ageing and depression. It is hoped that these findings will be able to inform both policy and practice to improve older adults’ care and support for depression.
目的对自我和他人的老龄化认知会对老年人的心理健康产生积极或消极的影响。本文旨在整合研究老年人对老龄化的认知与抑郁之间关系的文献,为老年人心理健康服务的实践和政策提供参考。设计/方法/途径通过在三个电子数据库中进行检索,同时进行正向和反向引文检索,确定了研究老年人对老龄化的认知与抑郁的定量研究文章。研究结果对老龄化的消极态度越严重,抑郁症状越严重;对老龄化的积极态度越严重,抑郁症状越轻或幸福感越高。但是,这种关系的因果方向无法确定。研究表明,对老龄化的看法也是抑郁症与健康状况、无望感和人格特质之间关系的调节因素。未来的研究应尝试研究老年人对老龄化的认知与抑郁之间的关系,以试图确定这种关系的因果方向。原创性/价值据作者所知,这是唯一一篇整合了探讨老年人对老龄化的认知与抑郁之间关系的文献的系统性综述。希望这些研究结果能够为政策和实践提供参考,以改善老年人对抑郁症的护理和支持。
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引用次数: 0
Cognitive functioning and life satisfaction as predictors of subjective health complaints in elderly people 认知功能和生活满意度是老年人主观健康抱怨的预测因素
IF 1.5 Q2 Nursing Pub Date : 2023-12-13 DOI: 10.1108/qaoa-08-2023-0055
Lídia Serra, Luís Silva
PurposeEffective cognitive functioning elucidates the orchestrated interplay of diverse mental faculties in addressing daily tasks, potentially indicative of an improved state of an individual’s health. Linked to this is the potential role of life satisfaction, which may aid individuals in better managing their health-related challenges. The purpose this study is to examine whether the cognitive functioning and life satisfaction levels of elderly individuals serve as predictors of their subjective health complaints.Design/methodology/approachThe research involved a cohort of 126 elderly community residents. The assessment tools used encompassed a socio-demographic questionnaire, the mini-mental state examination (MMSE), the scale of subjective health complaints and a life satisfaction scale.FindingsThe findings reveal that both cognitive functioning and life satisfaction are predictive variables for subjective health complaints, validated in both the original sample and simulated samples.Originality/valueThis study’s innovation lies in highlighting the importance of cognitive functioning and life satisfaction among the elderly population as explanatory factors for subjective health complaints. Consequently, these dimensions warrant consideration in specialized intervention programs aimed at promoting the health and quality of life among the elderly.
目的有效的认知功能阐明了在处理日常任务时各种心智能力的协调相互作用,这可能表明个人的健康状况有所改善。与此相关的是生活满意度的潜在作用,它可以帮助个人更好地应对与健康有关的挑战。本研究的目的是探讨老年人的认知功能和生活满意度水平是否可以预测他们的主观健康抱怨。研究结果研究结果显示,认知功能和生活满意度都是主观健康投诉的预测变量,这在原始样本和模拟样本中都得到了验证。原创性/价值本研究的创新之处在于强调了认知功能和生活满意度在老年人群中作为主观健康投诉解释因素的重要性。因此,在旨在促进老年人健康和提高其生活质量的专门干预计划中,这些方面值得考虑。
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引用次数: 0
Editorial: Recognising new partners and activities in older peoples’ care but also potential burdens in new forms of care and research 社论:认识到老年人护理中的新伙伴和新活动,但也认识到新形式护理和研究中的潜在负担
IF 1.5 Q2 Nursing Pub Date : 2023-12-01 DOI: 10.1108/qaoa-12-2023-097
Fiona Mary Poland
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引用次数: 0
“What have YOU done in the past few years?” Deaf BSL users’ experiences of caring for people with dementia during COVID-19 "您在过去几年中做了什么?聋人 BSL 使用者在 COVID-19 期间照顾痴呆症患者的经历
IF 1.5 Q2 Nursing Pub Date : 2023-11-27 DOI: 10.1108/qaoa-07-2023-0048
E. Ferguson-Coleman, Alys Young
Purpose Deaf people, who are British Sign Language (BSL) users, are, at times, carers for their parent or spouse when they have dementia. This can be a challenging role for the wider population, but if the common language in service provision is not one you share, then this care can be impacted by the lack of formal structures that support the Deaf caring role. This study aims to explore the experiences of Deaf carers supporting people with dementia, in an unpaid role, during the COVID-19 pandemic to understand more about their potential support preferences. Design/methodology/approach Online interviews with seven Deaf carers sharing their experiences of supporting their family member with dementia happened during the first year of the COVID-19 pandemic. Interpretive phenomenological analysis was used to qualitatively examine each Deaf carers’ stories. Findings Findings included Deaf carers’ lack of access to information, surrendering their autonomy to hearing family members to communicate with health-care professionals, with overarching isolation within local communities and online. Findings show a widespread infrastructural failure to meet the linguistic and specific support needs of this minority population. Research limitations/implications Seven Deaf carers took part in this study. This means the findings may not be generalisable. Practical implications Health-care professionals and social care structures need to develop robust clear communication pathways for Deaf carers to receive the support needed to provide effective care. Social implications If health-care professionals undertake training about Deaf people and BSL, that will mean Deaf carers will receive effective support to be able to care for a person living with dementia. This means that their Deaf identity will be recognised within the mainstream and the care provided will be much more effective for the person with dementia. Originality/value To the best of the authors’ knowledge, these are the first interviews undertaken with Deaf carers of people with dementia during the COVID-19 pandemic and its subsequent lockdowns. Understanding everyday barriers and social care limitations in terms of language access will enable Deaf carers to assert their rights and for care professionals to adapt their communication to match the individuals involved in the care package.
目的 使用英国手语 (BSL) 的聋人有时会照顾患有痴呆症的父母或配偶。对于更多的人来说,这可能是一个具有挑战性的角色,但如果提供服务的共同语言不是你们所共享的语言,那么这种照顾就会因缺乏支持聋人照顾角色的正式结构而受到影响。本研究旨在探讨聋人照护者在 COVID-19 大流行期间以无偿角色为痴呆症患者提供支持的经历,以进一步了解他们潜在的支持偏好。 设计/方法/途径 在 COVID-19 大流行的第一年,对七位聋人照护者进行了在线访谈,分享他们为痴呆症患者家人提供支持的经历。采用解释现象学分析法对每位聋人照护者的故事进行定性研究。 研究结果 研究结果显示,聋人照护者缺乏获取信息的渠道,在与医疗保健专业人员沟通时将自主权交给了听力健全的家庭成员,在当地社区和网络中被普遍孤立。研究结果表明,基础设施普遍无法满足这一少数群体在语言和特殊支持方面的需求。 研究局限性/影响 七名聋人照护者参与了本研究。这意味着研究结果可能不具有普遍性。 实际意义 医疗保健专业人员和社会护理机构需要为聋人照护者建立健全、清晰的沟通途径,以便他们获得所需的支持,提供有效的护理。 社会影响 如果医疗保健专业人员接受了有关聋人和 BSL 的培训,这将意味着聋人照护者将获得有效的支持,从而能够照护痴呆症患者。这意味着他们的聋人身份将得到主流社会的认可,为痴呆症患者提供的护理也将更加有效。 原创性/价值 据作者所知,这是在 COVID-19 大流行及随后的封锁期间对痴呆症患者的聋人照护者进行的首次访谈。了解日常障碍和社会护理在语言使用方面的限制,将有助于聋人照护者维护自己的权利,也有助于护理专业人员调整沟通方式,使之与护理方案中涉及的个人相匹配。
{"title":"“What have YOU done in the past few years?” Deaf BSL users’ experiences of caring for people with dementia during COVID-19","authors":"E. Ferguson-Coleman, Alys Young","doi":"10.1108/qaoa-07-2023-0048","DOIUrl":"https://doi.org/10.1108/qaoa-07-2023-0048","url":null,"abstract":"Purpose Deaf people, who are British Sign Language (BSL) users, are, at times, carers for their parent or spouse when they have dementia. This can be a challenging role for the wider population, but if the common language in service provision is not one you share, then this care can be impacted by the lack of formal structures that support the Deaf caring role. This study aims to explore the experiences of Deaf carers supporting people with dementia, in an unpaid role, during the COVID-19 pandemic to understand more about their potential support preferences. Design/methodology/approach Online interviews with seven Deaf carers sharing their experiences of supporting their family member with dementia happened during the first year of the COVID-19 pandemic. Interpretive phenomenological analysis was used to qualitatively examine each Deaf carers’ stories. Findings Findings included Deaf carers’ lack of access to information, surrendering their autonomy to hearing family members to communicate with health-care professionals, with overarching isolation within local communities and online. Findings show a widespread infrastructural failure to meet the linguistic and specific support needs of this minority population. Research limitations/implications Seven Deaf carers took part in this study. This means the findings may not be generalisable. Practical implications Health-care professionals and social care structures need to develop robust clear communication pathways for Deaf carers to receive the support needed to provide effective care. Social implications If health-care professionals undertake training about Deaf people and BSL, that will mean Deaf carers will receive effective support to be able to care for a person living with dementia. This means that their Deaf identity will be recognised within the mainstream and the care provided will be much more effective for the person with dementia. Originality/value To the best of the authors’ knowledge, these are the first interviews undertaken with Deaf carers of people with dementia during the COVID-19 pandemic and its subsequent lockdowns. Understanding everyday barriers and social care limitations in terms of language access will enable Deaf carers to assert their rights and for care professionals to adapt their communication to match the individuals involved in the care package.","PeriodicalId":44916,"journal":{"name":"Quality in Ageing and Older Adults","volume":null,"pages":null},"PeriodicalIF":1.5,"publicationDate":"2023-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139230682","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
Participatory action research on webs of caring in the digital age across four European countries 欧洲四个国家数字时代关怀网络的参与式行动研究
Q2 Nursing Pub Date : 2023-10-24 DOI: 10.1108/qaoa-03-2023-0020
Miranda Leontowitsch, Aivita Putnina, Marcus Andersson, Charlotta Niemistö, Rafaela Werny, Hanna Sjögren, Ilze Mileiko, Kārlis Lakševics, Artūrs Pokšāns, Māra Neikena, Līna Orste, Camilla Malm, Frank Oswald, Jeff Hearn, Clary Krekula
Purpose The digital age requires people of all ages to communicate and organise their lives through digital technologies. The project EQualCare investigates how the growing population of older people living alone is managing this transition, how it shapes their (non-)digital social networks and what changes on a local level need to be brought about. This paper aims to give insight into the process of participatory action research (PAR) with older people in the community across four countries and reflects on experiences made by academic and co-researchers. Design/methodology/approach Following the emancipatory underpinnings of PAR, which aims to reduce inequalities through collaboration and co-design, EQualCare involved nine teams of co-researchers across Finland, Germany, Latvia and Sweden making older people the centre of policy development. Co-researchers were involved in formulating research aims, collecting data, reflecting on data, formulating and disseminating recommendations for local policy stakeholders. Findings Co-researchers’ motivation to invest considerable time and effort was driven by a desire to create a more equal future for older people living alone. Moreover, they were keen to involve marginalised older people and became frustrated when this proved difficult. Power dynamics played a role throughout the process but became productive as roles and responsibilities were renegotiated. Doing PAR with older people can be emotionally challenging for co-researchers when negative feelings around ageing are encountered. Originality/value The paper advances understanding on the process of PAR in ageing research by reflecting on the social, cultural and political contexts of doing PAR with diverse sets of older people.
数字时代要求所有年龄段的人通过数字技术进行交流和组织他们的生活。EQualCare项目调查了越来越多的独居老人是如何应对这种转变的,这种转变如何塑造了他们的(非)数字社交网络,以及需要在地方层面上做出哪些改变。本文旨在深入了解四个国家社区老年人参与行动研究(PAR)的过程,并反思学术和合作研究人员的经验。根据旨在通过合作和共同设计减少不平等现象的PAR的解放基础,EQualCare项目涉及芬兰、德国、拉脱维亚和瑞典的九个共同研究团队,使老年人成为政策制定的中心。共同研究人员参与制定研究目标、收集数据、反思数据、为当地政策利益相关者制定和传播建议。共同研究人员投入大量时间和精力的动机是希望为独居老人创造一个更平等的未来。此外,他们热衷于让被边缘化的老年人参与进来,但当事实证明这很困难时,他们感到沮丧。权力动力学在整个过程中发挥了作用,但随着角色和责任的重新谈判,它变得富有成效。当遇到与衰老有关的负面情绪时,与老年人一起做PAR对共同研究人员来说可能是一种情感挑战。原创性/价值本文通过对不同老年人群体进行PAR的社会、文化和政治背景的反思,促进了对PAR在老龄化研究中的过程的理解。
{"title":"Participatory action research on webs of caring in the digital age across four European countries","authors":"Miranda Leontowitsch, Aivita Putnina, Marcus Andersson, Charlotta Niemistö, Rafaela Werny, Hanna Sjögren, Ilze Mileiko, Kārlis Lakševics, Artūrs Pokšāns, Māra Neikena, Līna Orste, Camilla Malm, Frank Oswald, Jeff Hearn, Clary Krekula","doi":"10.1108/qaoa-03-2023-0020","DOIUrl":"https://doi.org/10.1108/qaoa-03-2023-0020","url":null,"abstract":"Purpose The digital age requires people of all ages to communicate and organise their lives through digital technologies. The project EQualCare investigates how the growing population of older people living alone is managing this transition, how it shapes their (non-)digital social networks and what changes on a local level need to be brought about. This paper aims to give insight into the process of participatory action research (PAR) with older people in the community across four countries and reflects on experiences made by academic and co-researchers. Design/methodology/approach Following the emancipatory underpinnings of PAR, which aims to reduce inequalities through collaboration and co-design, EQualCare involved nine teams of co-researchers across Finland, Germany, Latvia and Sweden making older people the centre of policy development. Co-researchers were involved in formulating research aims, collecting data, reflecting on data, formulating and disseminating recommendations for local policy stakeholders. Findings Co-researchers’ motivation to invest considerable time and effort was driven by a desire to create a more equal future for older people living alone. Moreover, they were keen to involve marginalised older people and became frustrated when this proved difficult. Power dynamics played a role throughout the process but became productive as roles and responsibilities were renegotiated. Doing PAR with older people can be emotionally challenging for co-researchers when negative feelings around ageing are encountered. Originality/value The paper advances understanding on the process of PAR in ageing research by reflecting on the social, cultural and political contexts of doing PAR with diverse sets of older people.","PeriodicalId":44916,"journal":{"name":"Quality in Ageing and Older Adults","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135220088","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
Participatory action research and intersectionality: a critical dialogical reflection of a study with older adults 参与性行动研究和交叉性:对老年人研究的批判性对话反映
Q2 Nursing Pub Date : 2023-10-19 DOI: 10.1108/qaoa-03-2023-0024
Maaike Muntinga, Elena Bendien, Tineke Abma, Barbara Groot
Purpose Researchers who work in partnership with older adults in participatory studies often experience various advantages, but also complex ethical questions or even encounter obstacles during the research process. This paper aims to provide insights into the value of an intersectional lens in participatory research to understand how power plays out within a mixed research team of academic and community co-researchers. Design/methodology/approach Four academic researchers reflected in a case-study approach in a dialogical way on two critical case examples with the most learning potential by written dialogical and via face-to-face meetings in duos or trios. This study used an intersectionality-informed analysis. Findings This study shows that the intersectional lens helped the authors to understand the interactions of key players in the study and their different social locations. Intersections of age, gender, ethnicity/class and professional status stood out as categories in conflict. In hindsight, forms of privilege and oppression became more apparent. The authors also understood that they reproduced traditional power dynamics within the group of co-researchers and between academic and community co-researchers that did not match their mission for horizontal relations. This study showed that academics, although they wanted to work toward social inclusion and equality, were bystanders and people who reproduced power relations at several crucial moments. This was disempowering for certain older individuals and social groups and marginalized their voices and interests. Originality/value Till now, not many scholars wrote in-depth about race- and age-related tensions in partnerships in participatory action research or related approaches, especially not about tensions in research with older people.
在参与性研究中与老年人合作的研究人员通常会经历各种优势,但也会遇到复杂的伦理问题,甚至在研究过程中遇到障碍。本文旨在深入了解参与性研究中交叉镜头的价值,以了解权力如何在学术和社区共同研究人员的混合研究团队中发挥作用。设计/方法/方法四名学术研究人员以对话的方式对两个最具学习潜力的关键案例进行案例研究,通过书面对话和面对面的二人或三人会议。本研究采用了交叉性分析。本研究表明,交叉镜头有助于作者了解研究中关键参与者的相互作用以及他们不同的社会位置。年龄、性别、种族/阶级和职业地位的交叉点是冲突的类别。事后看来,特权和压迫的形式变得更加明显。作者还明白,他们在共同研究人员群体内以及学术和社区共同研究人员之间再现了传统的权力动态,这与他们的横向关系使命不符。这项研究表明,虽然学者们想要为社会包容和平等而努力,但他们是旁观者,是在几个关键时刻复制权力关系的人。这削弱了某些老年人和社会群体的权力,使他们的声音和利益被边缘化。独创性/价值到目前为止,对参与性行动研究或相关方法中的伙伴关系中与种族和年龄相关的紧张关系进行深入研究的学者并不多,特别是对老年人研究中的紧张关系的研究较少。
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引用次数: 0
Coping with the post-COVID-19 pandemic: perceived changes of older adults in their life satisfaction, depression, and quality of life 应对covid -19大流行后:老年人生活满意度、抑郁和生活质量的感知变化
Q2 Nursing Pub Date : 2023-09-29 DOI: 10.1108/qaoa-02-2023-0007
Bushra Rashid Al-Ghafri, Maram Qasim Al Nabhani, Hamed Al-Sinawi, Abdulaziz Al-Mahrezi, Zahir Badar Al Ghusaini, Ahmed Mohammed Al-Harrasi, Yaqoub Al-Saidi, Moon Fai Chan
Purpose As a result of the COVID-19 pandemic, many countries have implemented preventive measures that may negatively affect the physical and mental health of older adults. This study aims to investigate the changes in life satisfaction, depressive symptoms and quality-of-life (QoL) of older adults during the post-COVID-19 pandemic in Oman. Design/methodology/approach A prospective four-week follow-up study was conducted in one health-care center in Muscat, Oman. Convenience sampling was used, and the recruitment was from November 2021 to October 2022, with 38 participants aged 60–81, of whom 36 completed the study. The study evaluated changes in psychological well-being over time and analyzed gender differences. Findings The study revealed a positive impact of the preventive measures on the QoL (F = 3.08, p = 0.032) and a reduction in depressive symptoms (F = 3.09, p = 0.045). However, there was no significant change in life satisfaction (F = 1.90, p = 0.165). In particular, older women reported decreased depression (F = 5.31, p = 0.006), while older men reported improved QoL (F = 4.27, p = 0.025). Practical implications Few studies have reported on the well-being issues of older adults in Oman during the pandemic. Thus, the findings of this study can contribute to the international understanding of the impact of pandemics on the well-being of older adults in Oman and help health-care professionals tailor health-care programs for older adults in the community setting. Originality/value This study provides valuable insights into the well-being of older adults in Oman during the pandemic. Understanding the effects of long-term health hazards is crucial for developing community-level intervention plans and strategies for older adults in the community setting.
由于2019冠状病毒病大流行,许多国家实施了可能对老年人身心健康产生负面影响的预防措施。本研究旨在调查阿曼老年人在2019冠状病毒病大流行后生活满意度、抑郁症状和生活质量(QoL)的变化。设计/方法/方法在阿曼马斯喀特的一家保健中心进行了一项为期四周的前瞻性随访研究。采用方便抽样,招募时间为2021年11月至2022年10月,共有38名年龄在60-81岁之间的参与者,其中36人完成了研究。该研究评估了心理健康随时间的变化,并分析了性别差异。研究结果显示,预防措施对生活质量有积极影响(F = 3.08, p = 0.032),对抑郁症状有减轻作用(F = 3.09, p = 0.045)。然而,生活满意度没有显著变化(F = 1.90, p = 0.165)。特别是,老年女性报告抑郁减少(F = 5.31, p = 0.006),而老年男性报告生活质量改善(F = 4.27, p = 0.025)。实际影响很少有研究报告大流行期间阿曼老年人的福祉问题。因此,本研究的结果有助于国际上了解流行病对阿曼老年人福祉的影响,并帮助卫生保健专业人员为社区环境中的老年人量身定制卫生保健方案。独创性/价值本研究为大流行期间阿曼老年人的福祉提供了有价值的见解。了解长期健康危害的影响对于在社区环境中为老年人制定社区一级的干预计划和战略至关重要。
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引用次数: 0
Paws for thought? Developing dog projects for older people in prison 思考的爪子?为监狱中的老年人开发狗狗项目
IF 1.5 Q2 Nursing Pub Date : 2023-09-08 DOI: 10.1108/qaoa-11-2022-0069
Helen Codd
PurposeThis study aims to assess the nature and scope of dog-based programmes in prisons, assessing critically the potential opportunities, benefits, challenges and risks of developing innovative dog-based programmes for older prisoners in England and Wales. This paper outlines the potential benefits and challenges of developing dog-based programmes for older prisoners and sets out next steps for future research and practice.Design/methodology/approachThis study is based on a scoping review of published research literature on prison dog programmes (PDPs) in the USA, the UK and other countries, with particular reference to older people in prison, followed by semi-structured interviews with six members of an expert advisory group. The literature review and data from the qualitative interviews were analysed thematically.FindingsThere is a substantial body of published research literature which supports PDPs as having identifiable positive impacts for people and also dogs, and also published research which highlights the benefits to older people of dog ownership or participation in dog-based activities. However, much of this research is small-scale and qualitative, and it has been argued that there is a lack of a quantitative evidence base. This research concludes that findings from the literature review and the semi-structured interviews support further research and the creation of pilot projects to develop dog-based projects for older people in prison.Research limitations/implicationsThis study was small-scale, and the findings need to be approached with caution. The literature review searched a small number of databases and filtered out articles published in languages other than English, and the review of the grey literature focused on reports from the UK. The number of experts interviewed was small and there was no direct consultation with older people in prison nor with older people with recent personal lived experience of imprisonment and community resettlement. A more extensive future study would benefit from a more extensive literature review, a larger group of participants and the inclusion of service users, prison managers and government policymakers, subject to the appropriate ethical and security approvals. At the time the research took place, ongoing COVID-19 restrictions on prison research meant that research with current prisoners and prison managers would not have been approved by the HMPPS NRC.Practical implicationsThis research provides a research-based justification for future dog projects for older prisoners, leading potentially to improved well-being for older people in prison.Originality/valueThis study brings together the published research literature on PDPs with the research literature on the needs and experiences of older people in prison for the first time, and identifies potential directions for future research.
目的本研究旨在评估监狱中基于狗的计划的性质和范围,批判性地评估为英格兰和威尔士的老年囚犯开发创新的基于狗的项目的潜在机会、好处、挑战和风险。本文概述了为老年囚犯制定基于狗的计划的潜在好处和挑战,并为未来的研究和实践提出了下一步行动。设计/方法/方法本研究基于对美国、英国和其他国家已发表的监狱犬计划(PDP)研究文献的范围审查,特别是对监狱中的老年人的研究,然后对专家咨询小组的六名成员进行半结构化访谈。对文献综述和定性访谈的数据进行了主题分析。发现有大量已发表的研究文献支持PDP对人和狗都有可识别的积极影响,也有已发表的报告强调了养狗或参与以狗为基础的活动对老年人的好处。然而,这项研究大多是小规模的定性研究,有人认为缺乏定量的证据基础。这项研究的结论是,文献综述和半结构化访谈的结果支持进一步的研究和创建试点项目,为监狱中的老年人开发基于狗的项目。研究局限性/含义这项研究规模较小,需要谨慎对待研究结果。文献综述搜索了少量数据库,筛选出了以英语以外的语言发表的文章,灰色文献综述的重点是来自英国的报告。接受采访的专家人数很少,既没有与监狱中的老年人直接协商,也没有与最近有过监禁和社区安置个人生活经历的老年人协商。更广泛的未来研究将受益于更广泛的文献综述、更大的参与者群体以及服务使用者、监狱管理人员和政府决策者的参与,但需获得适当的道德和安全批准。在研究进行时,新冠肺炎对监狱研究的持续限制意味着HMPPS NRC不会批准对当前囚犯和监狱管理人员的研究。实际意义这项研究为未来老年囚犯的狗项目提供了基于研究的理由,有可能改善监狱中老年人的福祉。原创性/价值本研究首次将已发表的关于PDP的研究文献与关于监狱中老年人需求和经历的研究文献结合在一起,并确定了未来研究的潜在方向。
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Quality in Ageing and Older Adults
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