首页 > 最新文献

Health & Social Care in the Community最新文献

英文 中文
Assessment of Fatigue Levels Among Family Caregivers of Cancer Patients in a University Hospital 某大学医院肿瘤患者家属护理人员疲劳程度评估
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2026-01-08 DOI: 10.1155/hsc/5225127
Sibel Serçe, Özlem Ovayolu, Sevgi Kuyupınar Metin, Sümeyra Mihrap İlter

Background

Cancer is a challenging process that brings about negative physical, emotional, and social effects for both patients and their family caregivers. Caring for patients diagnosed with cancer by family members can be exhausting, especially when prolonged and intensive. Thus, it is crucial to assess family caregivers’ fatigue levels and create plans to ease that condition.

Methods

This descriptive study was conducted to assess the fatigue levels of family members of cancer patients. The population consisted of all cancer patients followed in the oncology clinic and outpatient clinic, while the sample included 199 family members caring for these patients according to the power analysis (α = 0.05 and 1 − β = 80%) and inclusion criteria, and the study was completed with 200 family caregivers of these patients. The data were collected using a questionnaire, developed by the researchers based on the literature review and the Piper Fatigue Scale (PFS).

Results

The findings of the study indicated that the PFS total mean score of the caregivers was 5.43 ± 2.21. Moreover, those who were female, were suffering from a chronic disease, had another family member to look after, cared for a patient with inadequate self-care, did not receive any care support from anyone else, stated that they had physical and economic problems due to care, thought that they neglected their other family members due to care responsibilities, and reported that caregiving negatively affected their social life/quality of life had higher PFS total mean scores (p < 0.05).

Conclusion

Consequently, it was found that family caregivers experienced moderate levels of fatigue. Furthermore, being a woman, caring for someone with a chronic illness other than cancer, and caring for someone who is unable to meet self-care needs are significant factors that exacerbate fatigue of caregivers. Therefore, it is crucial to identify the fatigue levels of family caregivers of cancer patients and provide them with the necessary support.

癌症是一个具有挑战性的过程,会给患者和他们的家庭照顾者带来负面的身体、情感和社会影响。照顾被家庭成员诊断为癌症的患者可能会让人筋疲力尽,尤其是在长期和密集的情况下。因此,评估家庭照顾者的疲劳程度并制定缓解这种情况的计划是至关重要的。方法对癌症患者家属的疲劳程度进行描述性研究。研究对象为肿瘤门诊和门诊随访的所有癌症患者,根据幂次分析(α = 0.05, 1 - β = 80%)和纳入标准,纳入199名照顾患者的家庭成员,并与200名患者的家庭照顾者一起完成研究。研究人员根据文献综述和Piper疲劳量表(PFS)编制了一份调查问卷,收集数据。结果护理人员的PFS总分平均为5.43±2.21分。此外,患有慢性疾病的女性、需要照顾另一名家庭成员、照顾自我照顾不足的病人、没有得到任何其他人的照顾支持、声称由于照顾而出现身体和经济问题、认为由于照顾责任而忽视了其他家庭成员。照料对其社会生活/生活质量有负面影响者的PFS总平均分较高(p < 0.05)。结论家庭照顾者的疲劳程度为中等。此外,作为一名女性,照顾患有癌症以外的慢性疾病的人,照顾无法满足自我照顾需求的人是加剧照顾者疲劳的重要因素。因此,确定癌症患者的家庭照顾者的疲劳程度,并为他们提供必要的支持是至关重要的。
{"title":"Assessment of Fatigue Levels Among Family Caregivers of Cancer Patients in a University Hospital","authors":"Sibel Serçe,&nbsp;Özlem Ovayolu,&nbsp;Sevgi Kuyupınar Metin,&nbsp;Sümeyra Mihrap İlter","doi":"10.1155/hsc/5225127","DOIUrl":"https://doi.org/10.1155/hsc/5225127","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Cancer is a challenging process that brings about negative physical, emotional, and social effects for both patients and their family caregivers. Caring for patients diagnosed with cancer by family members can be exhausting, especially when prolonged and intensive. Thus, it is crucial to assess family caregivers’ fatigue levels and create plans to ease that condition.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>This descriptive study was conducted to assess the fatigue levels of family members of cancer patients. The population consisted of all cancer patients followed in the oncology clinic and outpatient clinic, while the sample included 199 family members caring for these patients according to the power analysis (<i>α</i> = 0.05 and 1 − <i>β</i> = 80%) and inclusion criteria, and the study was completed with 200 family caregivers of these patients. The data were collected using a questionnaire, developed by the researchers based on the literature review and the Piper Fatigue Scale (PFS).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The findings of the study indicated that the PFS total mean score of the caregivers was 5.43 ± 2.21. Moreover, those who were female, were suffering from a chronic disease, had another family member to look after, cared for a patient with inadequate self-care, did not receive any care support from anyone else, stated that they had physical and economic problems due to care, thought that they neglected their other family members due to care responsibilities, and reported that caregiving negatively affected their social life/quality of life had higher PFS total mean scores (<i>p</i> &lt; 0.05).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Consequently, it was found that family caregivers experienced moderate levels of fatigue. Furthermore, being a woman, caring for someone with a chronic illness other than cancer, and caring for someone who is unable to meet self-care needs are significant factors that exacerbate fatigue of caregivers. Therefore, it is crucial to identify the fatigue levels of family caregivers of cancer patients and provide them with the necessary support.</p>\u0000 </section>\u0000 </div>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2026 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/5225127","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145986861","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of Essential Oil Aromatherapy on Sleep, Depression, and Well-Being Among Older Adults: Implications for Community Health and Social Care 精油芳香疗法对老年人睡眠、抑郁和幸福感的影响:对社区健康和社会护理的影响
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2026-01-05 DOI: 10.1155/hsc/6615339
Pei Fen Chiang, Kai-Lin Liang, Yu Chih Huang

Background

Population aging presents major healthcare challenges, with sleep disorders and late-life depression undermining older adults’ well-being. Aromatherapy, a nonpharmacological approach, shows potential in alleviating these conditions through olfactory stimulation of the limbic system, reducing stress and enhancing emotional balance.

Objectives

This study evaluated the effects of essential oil aromatherapy on sleep quality, depression, and subjective well-being among older adults in long-term care facilities.

Methods

A quasiexperimental study was conducted in six facilities from January to April 2024. Ninety residents were assigned to weekly or monthly aromatherapy groups or a control group. Interventions lasted three months and used 30 essential oils. Outcomes were measured with the Pittsburgh Sleep Quality Index, World Health Organization–Five Well-Being Index, and Geriatric Depression Scale.

Results

Weekly aromatherapy significantly improved sleep latency, reduced sleep disturbance, and enhanced well-being in feelings of refreshment, interest, and happiness. Both weekly and monthly sessions reduced depressive symptoms. Regression analysis showed stronger improvements among males, while advancing age was negatively associated with outcomes.

Conclusions

Regular aromatherapy sessions can improve sleep, reduce depression, and enhance well-being in older adults. Beyond clinical effects, the findings highlight social care implications: incorporating low-cost, accessible interventions into long-term care routines may foster social interaction, emotional support, and residents’ sense of belonging, contributing to holistic and community-oriented elder care.

人口老龄化带来了重大的医疗保健挑战,睡眠障碍和晚年抑郁症损害了老年人的健康。芳香疗法,一种非药物疗法,显示出通过嗅觉刺激边缘系统,减轻压力和增强情绪平衡来缓解这些疾病的潜力。目的本研究评估了精油芳香疗法对长期护理机构中老年人睡眠质量、抑郁和主观幸福感的影响。方法于2024年1 - 4月在6家医院进行准实验研究。90名居民被分配到每周一次或每月一次的芳香疗法组或对照组。干预持续了三个月,使用了30种精油。结果用匹兹堡睡眠质量指数、世界卫生组织五幸福指数和老年抑郁症量表来衡量。结果每周芳香疗法可显著改善睡眠潜伏期,减少睡眠障碍,增强精神状态、兴趣和幸福感。每周和每月的治疗都能减轻抑郁症状。回归分析显示,男性的改善更明显,而年龄的增长与结果呈负相关。结论:定期的芳香疗法可以改善老年人的睡眠,减少抑郁,提高幸福感。除了临床效果外,研究结果还强调了社会护理的意义:将低成本,可获得的干预措施纳入长期护理程序可能会促进社会互动,情感支持和居民的归属感,有助于整体和社区导向的老年护理。
{"title":"Effects of Essential Oil Aromatherapy on Sleep, Depression, and Well-Being Among Older Adults: Implications for Community Health and Social Care","authors":"Pei Fen Chiang,&nbsp;Kai-Lin Liang,&nbsp;Yu Chih Huang","doi":"10.1155/hsc/6615339","DOIUrl":"https://doi.org/10.1155/hsc/6615339","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Population aging presents major healthcare challenges, with sleep disorders and late-life depression undermining older adults’ well-being. Aromatherapy, a nonpharmacological approach, shows potential in alleviating these conditions through olfactory stimulation of the limbic system, reducing stress and enhancing emotional balance.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>This study evaluated the effects of essential oil aromatherapy on sleep quality, depression, and subjective well-being among older adults in long-term care facilities.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A quasiexperimental study was conducted in six facilities from January to April 2024. Ninety residents were assigned to weekly or monthly aromatherapy groups or a control group. Interventions lasted three months and used 30 essential oils. Outcomes were measured with the Pittsburgh Sleep Quality Index, World Health Organization–Five Well-Being Index, and Geriatric Depression Scale.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Weekly aromatherapy significantly improved sleep latency, reduced sleep disturbance, and enhanced well-being in feelings of refreshment, interest, and happiness. Both weekly and monthly sessions reduced depressive symptoms. Regression analysis showed stronger improvements among males, while advancing age was negatively associated with outcomes.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Regular aromatherapy sessions can improve sleep, reduce depression, and enhance well-being in older adults. Beyond clinical effects, the findings highlight social care implications: incorporating low-cost, accessible interventions into long-term care routines may foster social interaction, emotional support, and residents’ sense of belonging, contributing to holistic and community-oriented elder care.</p>\u0000 </section>\u0000 </div>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2026 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2026-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/6615339","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145904863","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Foundations of Social Work Practice in Paediatric Palliative Care From the Perspective of the Patient, the Family and the Multidisciplinary Team: A Systematic Review 从患者、家庭和多学科团队的角度看儿科姑息治疗的社会工作实践基础:系统回顾
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2026-01-04 DOI: 10.1155/hsc/8849933
M. Elena Cuartero-Castañer, Ana J. Cañas-Lerma, Sara Bagur, Sebastià Verger

Paediatric palliative care is a complex and painful reality for children, young people and their families, and the professional team caring for them. Social workers are essential in these teams, providing emotional and care support to patients and their families. Each country and hospital have its characteristics, but there needs to be more general information to determine the essential aspects on which social work practice is based. This systematic review aims to identify the theoretical underpinnings of social work in paediatric palliative care to develop a knowledge framework for future intervention strategies. The systematic review included 14 studies between 2018 and 2023, identified by searching four databases using the PRISMA methodology (WOS, SCOPUS, Dialnet Plus and ERIC). From the analysis of the articles, 13 categories were identified as fundamental to the social work approach in the context of paediatric palliative care. These foundations include relational and caring practices and work with the family, main theoretical models, cultural aspects and multidisciplinary work, among others. In addition, new challenges, such as social work with groups and telehealth, are addressed. The findings of this systematic review provide strategic and research directions for social workers working in paediatric palliative care, thus contributing to the profession’s development in this field.

儿科姑息治疗对于儿童、年轻人及其家庭以及照顾他们的专业团队来说是一个复杂而痛苦的现实。社会工作者在这些团队中是必不可少的,为患者及其家属提供情感和护理支持。每个国家和医院都有自己的特点,但需要更多的一般信息来确定社会工作实践所依据的基本方面。本系统综述旨在确定儿科姑息治疗中社会工作的理论基础,为未来的干预策略制定知识框架。系统评价包括2018年至2023年期间的14项研究,通过使用PRISMA方法检索四个数据库(WOS, SCOPUS, Dialnet Plus和ERIC)确定。从文章的分析中,13个类别被确定为在儿科姑息治疗背景下社会工作方法的基础。这些基础包括关系和护理实践以及与家庭的合作、主要理论模型、文化方面和多学科工作等。此外,还处理了新的挑战,如团体社会工作和远程保健。本系统综述的研究结果为从事儿科姑息治疗的社会工作者提供了策略和研究方向,从而有助于该领域的专业发展。
{"title":"Foundations of Social Work Practice in Paediatric Palliative Care From the Perspective of the Patient, the Family and the Multidisciplinary Team: A Systematic Review","authors":"M. Elena Cuartero-Castañer,&nbsp;Ana J. Cañas-Lerma,&nbsp;Sara Bagur,&nbsp;Sebastià Verger","doi":"10.1155/hsc/8849933","DOIUrl":"https://doi.org/10.1155/hsc/8849933","url":null,"abstract":"<p>Paediatric palliative care is a complex and painful reality for children, young people and their families, and the professional team caring for them. Social workers are essential in these teams, providing emotional and care support to patients and their families. Each country and hospital have its characteristics, but there needs to be more general information to determine the essential aspects on which social work practice is based. This systematic review aims to identify the theoretical underpinnings of social work in paediatric palliative care to develop a knowledge framework for future intervention strategies. The systematic review included 14 studies between 2018 and 2023, identified by searching four databases using the PRISMA methodology (WOS, SCOPUS, Dialnet Plus and ERIC). From the analysis of the articles, 13 categories were identified as fundamental to the social work approach in the context of paediatric palliative care. These foundations include relational and caring practices and work with the family, main theoretical models, cultural aspects and multidisciplinary work, among others. In addition, new challenges, such as social work with groups and telehealth, are addressed. The findings of this systematic review provide strategic and research directions for social workers working in paediatric palliative care, thus contributing to the profession’s development in this field.</p>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2026 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2026-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/8849933","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145909342","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Engaging in Communication to Promote Healthy Ageing: Home Visitors’ Perspective on the Utilisation of Information From Preventive Home Visits 参与沟通促进康健乐颐年:家访者如何运用预防性家访的资讯
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2026-01-04 DOI: 10.1155/hsc/8842580
Anna Nivestam, Maria Haak, Albert Westergren, Gita Hedin

Background

To promote healthy ageing, it is crucial to involve older adults in social planning. Preventive home visits allow older adults to express their opinions, with home visitors playing a key role in gathering and relaying this information to decision-makers. Thus, highlighting the perspectives of home visitors is essential for maximising the utility of the collected information. Therefore, the purpose of this study was to gain a deeper understanding of important aspects regarding the utilisation of information from preventive home visits to create a society that promotes healthy ageing.

Methods

Five online focus group discussions were conducted with 16 home visitors from 15 municipalities representing various parts of Sweden. The discussion material was analysed with a focus on the content of the discussions.

Results

The analysis resulted in a main category: engaging in communication to promote healthy ageing—acting as the ‘spider in the web’ and advocating for older adults. Five subcategories were identified, highlighting the utilisation of information from preventive home visits for promoting healthy ageing: using older adults’ needs and capabilities as a starting point; empowering older adults to make their voices heard; compiling information to efficiently reach out; having people in leading positions close by; and receiving feedback on proposals.

Conclusions

Utilising information from preventive home visits to promote healthy ageing requires engagement from the home visitor, the older adults and a committed organisation. One critical aspect is the dialogue during the visit, which empowers the older adult and enables the home visitor to obtain information. Another important aspect is the home visitor’s engagement in communicating the information to actors who can promote healthy ageing in society. Finally, an organisation where leaders are available and give feedback on proposals based on information compiled during home visits is essential to promote healthy ageing.

背景:为了促进健康老龄化,让老年人参与社会规划至关重要。预防性家访使老年人能够表达他们的意见,家访人员在收集和向决策者传达这些信息方面发挥了关键作用。因此,强调家庭访客的观点对于最大限度地利用所收集的信息至关重要。因此,这项研究的目的是更深入地了解利用预防性家访信息的重要方面,以创建一个促进健康老龄化的社会。方法对来自瑞典不同地区的15个城市的16名家庭访问者进行了5次在线焦点小组讨论。对讨论材料进行了分析,重点是讨论的内容。结果分析得出一个主要类别:参与促进健康老龄化的交流-扮演“网络中的蜘蛛”并倡导老年人。确定了五个子类别,突出强调利用预防性家访信息促进健康老龄化:以老年人的需求和能力为起点;使老年人能够发出自己的声音;整理信息,有效推广;附近有领导人员的;并接受对提案的反馈。结论:利用预防性家访的信息来促进健康老龄化需要家访者、老年人和一个承诺的组织的参与。一个关键的方面是访问期间的对话,它赋予老年人权力,使家访者能够获得信息。另一个重要方面是家访人员参与向能够促进社会健康老龄化的行动者传播信息。最后,建立一个组织,让领导人根据家访期间收集的信息对建议提供反馈,这对促进健康老龄化至关重要。
{"title":"Engaging in Communication to Promote Healthy Ageing: Home Visitors’ Perspective on the Utilisation of Information From Preventive Home Visits","authors":"Anna Nivestam,&nbsp;Maria Haak,&nbsp;Albert Westergren,&nbsp;Gita Hedin","doi":"10.1155/hsc/8842580","DOIUrl":"https://doi.org/10.1155/hsc/8842580","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>To promote healthy ageing, it is crucial to involve older adults in social planning. Preventive home visits allow older adults to express their opinions, with home visitors playing a key role in gathering and relaying this information to decision-makers. Thus, highlighting the perspectives of home visitors is essential for maximising the utility of the collected information. Therefore, the purpose of this study was to gain a deeper understanding of important aspects regarding the utilisation of information from preventive home visits to create a society that promotes healthy ageing.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>Five online focus group discussions were conducted with 16 home visitors from 15 municipalities representing various parts of Sweden. The discussion material was analysed with a focus on the content of the discussions.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The analysis resulted in a main category: <i>engaging in communication to promote healthy ageing—acting as the ‘spider in the web’ and advocating for older adults</i>. Five subcategories were identified, highlighting the utilisation of information from preventive home visits for promoting healthy ageing: <i>using older adults’ needs and capabilities as a starting point</i>; <i>empowering older adults to make their voices heard</i>; <i>compiling information to efficiently reach out</i>; <i>having people in leading positions close by</i>; and <i>receiving feedback on proposals.</i></p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>Utilising information from preventive home visits to promote healthy ageing requires engagement from the home visitor, the older adults and a committed organisation. One critical aspect is the dialogue during the visit, which empowers the older adult and enables the home visitor to obtain information. Another important aspect is the home visitor’s engagement in communicating the information to actors who can promote healthy ageing in society. Finally, an organisation where leaders are available and give feedback on proposals based on information compiled during home visits is essential to promote healthy ageing.</p>\u0000 </section>\u0000 </div>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2026 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2026-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/8842580","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145904641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Social Support, Mental Health, and Quality of Life in Women Experiencing Infertility: A Systematic Review 不孕症妇女的社会支持、心理健康和生活质量:系统综述
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-31 DOI: 10.1155/hsc/6848207
Bentolhoda Ghasemi, Hedyeh Riazi, Seideh Hanieh Alamolhoda, Ali Montazeri

Background

Women experiencing infertility often report lower perceived social support, compromised mental health, and reduced quality of life. Understanding the interrelationships among these factors is essential for developing effective interventions and improving support systems for women facing infertility. This systematic review explores the associations between perceived social support and mental health with quality of life in women with infertility.

Methods

A comprehensive search was conducted across six databases—PubMed, ScienceDirect, Scopus, Web of Science, Embase, and Google Scholar—without time restrictions. Keywords included “social support,” “mental health,” “quality of life,” and “infertility.” Studies that met the inclusion criteria were reviewed and analyzed narratively.

Results

In total, 1080 articles were retrieved. After removing duplicates and irrelevant studies, 31 articles were included in the final analysis, of which 90% were cross-sectional. The result highlighted a positive relationship between perceived social support and quality of life, as well as between mental health and quality of life. Based on these findings, a theoretical model was developed to integrate these findings and illustrate the direct and indirect pathways through which perceived social support may influence quality of life via improved mental health.

Conclusions

The findings indicate that perceived social support and mental health are significantly associated with better quality of life in women with infertility. The proposed theoretical model provides a framework to understand these interactions and can inform future research and targeted psychosocial interventions.

经历不孕症的妇女通常报告认为社会支持较低,心理健康受损,生活质量下降。了解这些因素之间的相互关系对于制定有效的干预措施和改善对面临不孕症的妇女的支持系统至关重要。本系统综述探讨感知社会支持和心理健康与不孕妇女生活质量之间的关系。方法在pubmed、ScienceDirect、Scopus、Web of Science、Embase和谷歌scholar 6个数据库中进行综合检索,不受时间限制。关键词包括“社会支持”、“心理健康”、“生活质量”和“不孕症”。对符合纳入标准的研究进行综述和叙述性分析。结果共检索文献1080篇。在剔除重复和不相关研究后,31篇文章被纳入最终分析,其中90%是横断面研究。研究结果强调了感知到的社会支持与生活质量之间,以及心理健康与生活质量之间的正相关关系。基于这些发现,我们开发了一个理论模型来整合这些发现,并说明感知到的社会支持可能通过改善心理健康来影响生活质量的直接和间接途径。结论认知社会支持和心理健康与不孕妇女生活质量的提高有显著关系。提出的理论模型为理解这些相互作用提供了一个框架,可以为未来的研究和有针对性的社会心理干预提供信息。
{"title":"Social Support, Mental Health, and Quality of Life in Women Experiencing Infertility: A Systematic Review","authors":"Bentolhoda Ghasemi,&nbsp;Hedyeh Riazi,&nbsp;Seideh Hanieh Alamolhoda,&nbsp;Ali Montazeri","doi":"10.1155/hsc/6848207","DOIUrl":"https://doi.org/10.1155/hsc/6848207","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Women experiencing infertility often report lower perceived social support, compromised mental health, and reduced quality of life. Understanding the interrelationships among these factors is essential for developing effective interventions and improving support systems for women facing infertility. This systematic review explores the associations between perceived social support and mental health with quality of life in women with infertility.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A comprehensive search was conducted across six databases—PubMed, ScienceDirect, Scopus, Web of Science, Embase, and Google Scholar—without time restrictions. Keywords included “social support,” “mental health,” “quality of life,” and “infertility.” Studies that met the inclusion criteria were reviewed and analyzed narratively.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>In total, 1080 articles were retrieved. After removing duplicates and irrelevant studies, 31 articles were included in the final analysis, of which 90% were cross-sectional. The result highlighted a positive relationship between perceived social support and quality of life, as well as between mental health and quality of life. Based on these findings, a theoretical model was developed to integrate these findings and illustrate the direct and indirect pathways through which perceived social support may influence quality of life via improved mental health.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>The findings indicate that perceived social support and mental health are significantly associated with better quality of life in women with infertility. The proposed theoretical model provides a framework to understand these interactions and can inform future research and targeted psychosocial interventions.</p>\u0000 </section>\u0000 </div>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2025 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/6848207","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145887648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Caregiver Burden and Psychological Distress in Family Caregivers of Disabled Older Adults: Rumination as Mediator and Psychological Detachment as Moderator: A Cross-Sectional Study 残障老年人家庭照顾者的照顾负担与心理困扰:反刍为中介,心理超然为调节:一项横断面研究
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-30 DOI: 10.1155/hsc/2999118
Xiaofen Wang, Jingwen Yi, Yichen Geng, Yu Long, Danyan Li, Haiyan Liu, Miliang Zou, Pingping He, Guojun Wang

Objective

The high prevalence of psychological distress among caregivers of disabled elderly is well established, but the psychological mechanisms linking caregiver burden to distress are less understood. This study investigated the mediating role of rumination and moderating effect of psychological detachment in this relationship.

Method

From April to October 2024, we conducted a cross-sectional survey of 515 primary caregivers (mean age = 52.6 ± 11.0 years; 60.0% female) from community health centers in Changsha, China. Participants completed the Zarit Burden Interview (ZBI-12), rumination scale, psychological detachment scale (PDS), and Kessler psychological distress scale (K10). Data were analyzed using SPSS with Hayes’s PROCESS macro to examine moderated mediation effects, controlling for conceptually justified covariates.

Results

Caregiver burden was significantly associated with psychological distress both directly (β = 0.36, p < 0.001) and indirectly through rumination (β = 0.20, 95% bootstrap CI [0.16, 0.25]), which accounted for 35.3% of the total effect. Psychological detachment showed negative correlations with rumination (β = −0.59, p < 0.001) and psychological distress (β = −0.50, p < 0.001), while significantly moderating both the burden–rumination (β = −0.10, p = 0.004) and rumination–distress relationships (β = −0.10, p = 0.004).

Conclusion

The findings demonstrate that among caregivers of disabled older adults, caregiver burden is associated with psychological distress both directly and through rumination, while psychological detachment functions as a protective factor. By establishing these key mechanisms, this study provides a foundation for developing evidence-based interventions that simultaneously address rumination reduction and detachment enhancement to improve mental health in this vulnerable population.

目的残疾老年人照顾者心理困扰发生率高,但对照顾者负担与心理困扰之间的关系的心理机制尚不清楚。本研究探讨了反刍的中介作用和心理超然的调节作用。方法于2024年4 - 10月对长沙市社区卫生服务中心的515名初级护理人员(平均年龄52.6±11.0岁,女性60.0%)进行横断面调查。参与者完成了Zarit负担访谈(ZBI-12)、反刍量表、心理超脱量表(PDS)和Kessler心理困扰量表(K10)。数据分析使用SPSS和Hayes 's PROCESS宏来检查调节的中介效应,控制概念上合理的协变量。结果照顾者负担与心理困扰的直接相关(β = 0.36, p < 0.001)和反刍间接相关(β = 0.20, 95% bootstrap CI[0.16, 0.25])占总效应的35.3%。心理超脱与反刍(β = - 0.59, p < 0.001)和心理困扰(β = - 0.50, p < 0.001)呈负相关,而对负担-反刍(β = - 0.10, p = 0.004)和反刍-困扰关系(β = - 0.10, p = 0.004)均有显著调节作用。结论在残疾老年人照顾者中,照顾者负担与心理困扰存在直接和反刍关系,而心理超脱则起保护作用。通过建立这些关键机制,本研究为开发基于证据的干预措施提供了基础,这些干预措施可以同时解决反刍减少和超然增强的问题,从而改善弱势群体的心理健康。
{"title":"Caregiver Burden and Psychological Distress in Family Caregivers of Disabled Older Adults: Rumination as Mediator and Psychological Detachment as Moderator: A Cross-Sectional Study","authors":"Xiaofen Wang,&nbsp;Jingwen Yi,&nbsp;Yichen Geng,&nbsp;Yu Long,&nbsp;Danyan Li,&nbsp;Haiyan Liu,&nbsp;Miliang Zou,&nbsp;Pingping He,&nbsp;Guojun Wang","doi":"10.1155/hsc/2999118","DOIUrl":"https://doi.org/10.1155/hsc/2999118","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>The high prevalence of psychological distress among caregivers of disabled elderly is well established, but the psychological mechanisms linking caregiver burden to distress are less understood. This study investigated the mediating role of rumination and moderating effect of psychological detachment in this relationship.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Method</h3>\u0000 \u0000 <p>From April to October 2024, we conducted a cross-sectional survey of 515 primary caregivers (mean age = 52.6 ± 11.0 years; 60.0% female) from community health centers in Changsha, China. Participants completed the Zarit Burden Interview (ZBI-12), rumination scale, psychological detachment scale (PDS), and Kessler psychological distress scale (K10). Data were analyzed using SPSS with Hayes’s PROCESS macro to examine moderated mediation effects, controlling for conceptually justified covariates.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Caregiver burden was significantly associated with psychological distress both directly (<i>β</i> = 0.36, <i>p</i> &lt; 0.001) and indirectly through rumination (<i>β</i> = 0.20, 95% bootstrap CI [0.16, 0.25]), which accounted for 35.3% of the total effect. Psychological detachment showed negative correlations with rumination (<i>β</i> = −0.59, <i>p</i> &lt; 0.001) and psychological distress (<i>β</i> = −0.50, <i>p</i> &lt; 0.001), while significantly moderating both the burden–rumination (<i>β</i> = −0.10, <i>p</i> = 0.004) and rumination–distress relationships (<i>β</i> = −0.10, <i>p</i> = 0.004).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The findings demonstrate that among caregivers of disabled older adults, caregiver burden is associated with psychological distress both directly and through rumination, while psychological detachment functions as a protective factor. By establishing these key mechanisms, this study provides a foundation for developing evidence-based interventions that simultaneously address rumination reduction and detachment enhancement to improve mental health in this vulnerable population.</p>\u0000 </section>\u0000 </div>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2025 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/2999118","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145887849","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sociocultural Dimensions of Community-Based Palliative Care in Brazil and Indonesia: An Ethnographic Study 基于社区的姑息治疗在巴西和印度尼西亚的社会文化维度:一项民族志研究
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-30 DOI: 10.1155/hsc/4624886
Annemarie Samuels, Hanum Atikasari, Natashe Lemos Dekker

Background

Palliative care services are increasingly implemented in diverse sociocultural settings around the world.

Aim

Our ethnographic project aimed to explore the sociocultural and organizational dimensions of community-based palliative care in Brazil and Indonesia.

Methods

We used ethnographic research methods to study local models of palliative care provision in Brazil and Indonesia. These countries were chosen because of similarities in stages of palliative care service development and yet differences in healthcare organization and dominant religion. After scoping initiatives, in each country, one thriving community-based initiative was selected for an in-depth case study through semistructured interviews and participant observation. Thematic analysis was first done for the individual cases and then compared across cases in team meetings.

Results

The case studies of community-based initiatives reveal (1) how local values are included in the development and practice of palliative care; (2) how these initiatives build on existing local health care structures; and (3) how local palliative care workers introduce the term “palliative care” with sensitivity to the local cultural context.

Conclusion

As palliative care services are implemented in various sociocultural settings, a better understanding of successful community-based models for palliative care provision is needed to adapt services to local contexts.

姑息治疗服务越来越多地在世界各地不同的社会文化环境中实施。我们的民族志项目旨在探索巴西和印度尼西亚社区姑息治疗的社会文化和组织层面。方法采用民族志研究方法对巴西和印度尼西亚的当地姑息治疗模式进行研究。选择这些国家是因为在姑息治疗服务发展阶段的相似之处,但在医疗保健组织和主要宗教方面存在差异。在确定倡议范围后,在每个国家,通过半结构化访谈和参与者观察,选择一个蓬勃发展的社区倡议进行深入的案例研究。首先对个别案例进行专题分析,然后在团队会议上进行跨案例比较。结果以社区为基础的案例研究揭示了(1)如何将地方价值观纳入姑息治疗的发展和实践;(2)这些举措如何以现有的地方卫生保健结构为基础;(3)当地的姑息治疗工作者如何在对当地文化语境敏感的情况下引入“姑息治疗”一词。随着姑息治疗服务在不同的社会文化背景下实施,需要更好地了解社区姑息治疗提供的成功模式,以使服务适应当地情况。
{"title":"Sociocultural Dimensions of Community-Based Palliative Care in Brazil and Indonesia: An Ethnographic Study","authors":"Annemarie Samuels,&nbsp;Hanum Atikasari,&nbsp;Natashe Lemos Dekker","doi":"10.1155/hsc/4624886","DOIUrl":"https://doi.org/10.1155/hsc/4624886","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Palliative care services are increasingly implemented in diverse sociocultural settings around the world.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Aim</h3>\u0000 \u0000 <p>Our ethnographic project aimed to explore the sociocultural and organizational dimensions of community-based palliative care in Brazil and Indonesia.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We used ethnographic research methods to study local models of palliative care provision in Brazil and Indonesia. These countries were chosen because of similarities in stages of palliative care service development and yet differences in healthcare organization and dominant religion. After scoping initiatives, in each country, one thriving community-based initiative was selected for an in-depth case study through semistructured interviews and participant observation. Thematic analysis was first done for the individual cases and then compared across cases in team meetings.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The case studies of community-based initiatives reveal (1) how local values are included in the development and practice of palliative care; (2) how these initiatives build on existing local health care structures; and (3) how local palliative care workers introduce the term “palliative care” with sensitivity to the local cultural context.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>As palliative care services are implemented in various sociocultural settings, a better understanding of successful community-based models for palliative care provision is needed to adapt services to local contexts.</p>\u0000 </section>\u0000 </div>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2025 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/4624886","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145891647","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Collaborative Development of Obesity Intervention Strategies and Digital Tools in Denmark 丹麦肥胖干预策略和数字工具的协同发展
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-29 DOI: 10.1155/hsc/7834710
Arianna D’Ulizia, Alessia D’Andrea, Carlotta Antonelli, Aleksandra Davydova, Rikke Andersen, Gitte Ravn-Haren

This study examines the results of the application of a bottom-up approach for collaboratively developing effective strategies and digital solutions for obesity prevention and healthy behavior promotion in Denmark. The results of two rounds of participatory workshop sessions conducted in early 2024 involving different stakeholders and target users are described. The results of the study confirm that bottom-up approaches, coupled with technological innovation, constitute an effective instrument to address the socially context-dependent and complex nature of obesity. The codeveloped intervention strategies and digital tools offer evidence-based suggestions for policymakers, health practitioners, and developers who want to invest in sustainable, user-initiated approaches to preventing obesity.

本研究考察了在丹麦采用自下而上的方法协同制定有效的战略和数字解决方案,以预防肥胖和促进健康行为的结果。本文描述了在2024年初进行的涉及不同利益相关者和目标用户的两轮参与性研讨会的结果。研究结果证实,自下而上的方法,加上技术创新,是解决肥胖的社会背景依赖性和复杂性的有效工具。共同开发的干预策略和数字工具为希望投资于可持续的、用户发起的预防肥胖方法的政策制定者、卫生从业者和开发人员提供了基于证据的建议。
{"title":"Collaborative Development of Obesity Intervention Strategies and Digital Tools in Denmark","authors":"Arianna D’Ulizia,&nbsp;Alessia D’Andrea,&nbsp;Carlotta Antonelli,&nbsp;Aleksandra Davydova,&nbsp;Rikke Andersen,&nbsp;Gitte Ravn-Haren","doi":"10.1155/hsc/7834710","DOIUrl":"https://doi.org/10.1155/hsc/7834710","url":null,"abstract":"<p>This study examines the results of the application of a bottom-up approach for collaboratively developing effective strategies and digital solutions for obesity prevention and healthy behavior promotion in Denmark. The results of two rounds of participatory workshop sessions conducted in early 2024 involving different stakeholders and target users are described. The results of the study confirm that bottom-up approaches, coupled with technological innovation, constitute an effective instrument to address the socially context-dependent and complex nature of obesity. The codeveloped intervention strategies and digital tools offer evidence-based suggestions for policymakers, health practitioners, and developers who want to invest in sustainable, user-initiated approaches to preventing obesity.</p>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2025 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/7834710","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145891679","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Perceived Social Support Among Older Adults Residing in the Rohingya Refugee Camp in Bangladesh 孟加拉国罗兴亚难民营老年人的社会支持感知
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-29 DOI: 10.1155/hsc/1601865
Sabuj Kanti Mistry, Afsana Anwar, Uday Narayan Yadav, Md Nazmul Huda, Muhammad Anwar Hossain, Saruna Ghimire, Shovon Bhattacharjee, ARM Mehrab Ali, Tahera Ahmed, Probal Kumar Mondal, Abu Ansar Md Rizwan, Suvasish Das Shuvo, Simon Rosenbaum

Background

Older refugees often experience limited support due to restricted mobility, scarce resources and limited attention to their needs. This study examined perceived social support and its determinants among older adults living in the Rohingya refugee camp in Bangladesh.

Methods

A cross-sectional survey was conducted among Rohingya older adults aged ≥ 60 years in five subcamps of Cox’s Bazar, Bangladesh, between November and December 2021. Data were collected through face-to-face interviews using a questionnaire including the Multidimensional Scale of Perceived Social Support, alongside sociodemographic, health and lifestyle variables. Multiple logistic regression identified factors associated with perceived social support.

Results

Among 864 participants, more than half (53.7%) reported insufficient perceived social support. Factors independently associated with insufficient support included lack of engagement in income-generating activities (adjusted odds ratio [aOR]: 3.02 and 95% confidence interval [CI]: 1.79–5.10), living alone (aOR: 3.17 and 95% CI: 1.84–5.47), and having noncommunicable diseases (aOR: 1.78 and 95% CI: 1.35–2.36).

Implications

Findings highlight the need for targeted, integrated social support initiatives addressing socioeconomic and health challenges among Rohingya older adults, embedded within existing humanitarian services to promote their well-being and inclusion.

由于行动受限、资源稀缺和对其需求的关注有限,老年难民往往得到的支持有限。本研究调查了生活在孟加拉国罗兴亚难民营的老年人的感知社会支持及其决定因素。方法于2021年11月至12月对孟加拉国考克斯巴扎尔五个亚营中年龄≥60岁的罗兴亚老年人进行横断面调查。数据是通过面对面访谈收集的,使用的问卷包括多维感知社会支持量表,以及社会人口、健康和生活方式变量。多元逻辑回归确定了与感知社会支持相关的因素。结果在864名参与者中,超过一半(53.7%)的人表示感知到的社会支持不足。与支持不足独立相关的因素包括缺乏创收活动(调整优势比[aOR]: 3.02, 95%可信区间[CI]: 1.79-5.10)、独居(调整优势比[aOR]: 3.17, 95% CI: 1.84-5.47)和患有非传染性疾病(aOR: 1.78, 95% CI: 1.35-2.36)。调查结果强调,需要有针对性的综合社会支持举措,解决罗兴亚老年人面临的社会经济和健康挑战,并将其纳入现有的人道主义服务,以促进他们的福祉和包容。
{"title":"Perceived Social Support Among Older Adults Residing in the Rohingya Refugee Camp in Bangladesh","authors":"Sabuj Kanti Mistry,&nbsp;Afsana Anwar,&nbsp;Uday Narayan Yadav,&nbsp;Md Nazmul Huda,&nbsp;Muhammad Anwar Hossain,&nbsp;Saruna Ghimire,&nbsp;Shovon Bhattacharjee,&nbsp;ARM Mehrab Ali,&nbsp;Tahera Ahmed,&nbsp;Probal Kumar Mondal,&nbsp;Abu Ansar Md Rizwan,&nbsp;Suvasish Das Shuvo,&nbsp;Simon Rosenbaum","doi":"10.1155/hsc/1601865","DOIUrl":"https://doi.org/10.1155/hsc/1601865","url":null,"abstract":"<div>\u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Older refugees often experience limited support due to restricted mobility, scarce resources and limited attention to their needs. This study examined perceived social support and its determinants among older adults living in the Rohingya refugee camp in Bangladesh.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A cross-sectional survey was conducted among Rohingya older adults aged ≥ 60 years in five subcamps of Cox’s Bazar, Bangladesh, between November and December 2021. Data were collected through face-to-face interviews using a questionnaire including the Multidimensional Scale of Perceived Social Support, alongside sociodemographic, health and lifestyle variables. Multiple logistic regression identified factors associated with perceived social support.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Among 864 participants, more than half (53.7%) reported insufficient perceived social support. Factors independently associated with insufficient support included lack of engagement in income-generating activities (adjusted odds ratio [aOR]: 3.02 and 95% confidence interval [CI]: 1.79–5.10), living alone (aOR: 3.17 and 95% CI: 1.84–5.47), and having noncommunicable diseases (aOR: 1.78 and 95% CI: 1.35–2.36).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Implications</h3>\u0000 \u0000 <p>Findings highlight the need for targeted, integrated social support initiatives addressing socioeconomic and health challenges among Rohingya older adults, embedded within existing humanitarian services to promote their well-being and inclusion.</p>\u0000 </section>\u0000 </div>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2025 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/1601865","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145887811","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recovery Colleges in the UK and Australia—How Do They Compare? A Scoping Review 英国和澳大利亚的康复学院比较如何?范围检讨
IF 2.3 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Pub Date : 2025-12-28 DOI: 10.1155/hsc/8911346
Dianna G. Smith, Alyssa R. Morse, Amelia Gulliver, Lisa Brophy, Amelia Yazidjoglou, Terri Warner, Michelle Banfield

Recovery Colleges are still a relatively new form of mental health service in Australia. This review aimed to explore the current literature on Australian Recovery Colleges and compare this to information on the United Kingdom of Great Britain and Northern Ireland Recovery Colleges. This study followed the Joanna Briggs Institute scoping review guidelines. We searched PubMed, PsycINFO, Web of Science and Scopus for peer-reviewed articles. Grey literature was identified through a four-stage process. All types of literature in English were included with no restriction on publication date. The review included 54 Recovery College studies: 16 Australian and 38 UK. A lack of information on around half of the Australian Recovery Colleges made comparison with UK Colleges and adherence to the core characteristics of the model more uncertain than expected. However, information extracted about the Recovery College characteristics and outcomes was similar for both Australian and UK Colleges. Co-production, which values diverse experience, expertise or knowledge in an equal relationship, is a critical component in the implementation of Recovery Colleges. However, there were knowledge gaps in the role of co-production in College governance and everyday operation. The review also supports the importance of recovery orientation and the value of being an educational service providing co-learning, which is essential to challenging the attitudes, eroding the traditional power relationships and imparting real-life examples of the challenges and realities that people face in their recovery journeys. Further research on Australian Colleges is required to better understand their implementation and outcomes.

在澳大利亚,康复学院仍然是一种相对较新的心理健康服务形式。本综述旨在探讨澳大利亚康复学院的现有文献,并将其与英国和北爱尔兰康复学院的信息进行比较。这项研究遵循了乔安娜布里格斯研究所的范围审查指南。我们在PubMed、PsycINFO、Web of Science和Scopus上搜索同行评议的文章。灰色文献是通过四个阶段的过程确定的。所有类型的英文文献都包括在内,没有出版日期的限制。该综述包括54项康复学院研究:16项澳大利亚研究和38项英国研究。由于缺乏关于大约一半澳大利亚康复学院的信息,使得与英国大学的比较以及对该模式核心特征的坚持比预期的更加不确定。然而,从澳大利亚和英国大学中提取的关于康复学院特征和结果的信息是相似的。在平等的关系中重视不同经验、专长或知识的合作制作是实施康复学院的关键组成部分。然而,合作生产在大学治理和日常运作中的作用存在知识空白。报告还强调了恢复导向的重要性和提供共同学习的教育服务的价值,这对于挑战态度、侵蚀传统权力关系和传授人们在恢复过程中面临的挑战和现实的真实例子至关重要。为了更好地了解澳大利亚大学的实施和结果,需要进一步研究澳大利亚大学。
{"title":"Recovery Colleges in the UK and Australia—How Do They Compare? A Scoping Review","authors":"Dianna G. Smith,&nbsp;Alyssa R. Morse,&nbsp;Amelia Gulliver,&nbsp;Lisa Brophy,&nbsp;Amelia Yazidjoglou,&nbsp;Terri Warner,&nbsp;Michelle Banfield","doi":"10.1155/hsc/8911346","DOIUrl":"https://doi.org/10.1155/hsc/8911346","url":null,"abstract":"<p>Recovery Colleges are still a relatively new form of mental health service in Australia. This review aimed to explore the current literature on Australian Recovery Colleges and compare this to information on the United Kingdom of Great Britain and Northern Ireland Recovery Colleges. This study followed the Joanna Briggs Institute scoping review guidelines. We searched PubMed, PsycINFO, Web of Science and Scopus for peer-reviewed articles. Grey literature was identified through a four-stage process. All types of literature in English were included with no restriction on publication date. The review included 54 Recovery College studies: 16 Australian and 38 UK. A lack of information on around half of the Australian Recovery Colleges made comparison with UK Colleges and adherence to the core characteristics of the model more uncertain than expected. However, information extracted about the Recovery College characteristics and outcomes was similar for both Australian and UK Colleges. Co-production, which values diverse experience, expertise or knowledge in an equal relationship, is a critical component in the implementation of Recovery Colleges. However, there were knowledge gaps in the role of co-production in College governance and everyday operation. The review also supports the importance of recovery orientation and the value of being an educational service providing co-learning, which is essential to challenging the attitudes, eroding the traditional power relationships and imparting real-life examples of the challenges and realities that people face in their recovery journeys. Further research on Australian Colleges is required to better understand their implementation and outcomes.</p>","PeriodicalId":48195,"journal":{"name":"Health & Social Care in the Community","volume":"2025 1","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/hsc/8911346","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145891094","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Health & Social Care in the Community
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1