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Development and implementation of a supportive care model for cancer patients in the last days of life: A hospital-based program 癌症患者生命最后几天支持性护理模式的发展和实施:基于医院的项目
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2025-12-04 DOI: 10.1016/j.apjon.2025.100828
Xiaoting Hou , Renxiu Guo , Wenhua Yu , Ling Yuan , Guoxia Chen , Xiaoxiao Ma , Yujie Zhou , Xue Zhang , Li Liu , Yunhua Wang , Yuhan Lu

Objective

The quality of end-of-life care for cancer patients in China remains unsatisfactory, particularly during their last days and hours, highlighting an urgent need for improvement. This study is aimed to develop and implement a hospital-based quality improvement (QI) program to provide supportive care for terminally ill cancer patients, with the goal of improving the quality of death of cancer patients and family satisfaction.

Methods

This QI program primarily included three phases: developing evidence-based practice standards and related materials; conducting stratified training and providing the bundled supportive care strategies; and implementing quality supervision. The supportive care provided to terminally ill cancer patients and their families consists 30 bundled strategies divided into 5 parts: recognition and confirmation that the person may enter the last few days of life, end-of-life communication, patient-centered supportive care, family-centered supportive care and bereavement support for the family. The quality of death of cancer patients was assessed from the perspective of charge nurses and family members using the Good Death Inventory (GDI), and family satisfaction was evaluated using the Family Satisfaction with Advanced Cancer Care-2 (FAMCARE-2) scale.

Results

One hundred and fourteen patients from five hospitals located in Beijing, Nanjing, and Kunming were provided the supportive care between May 2023 to August 2024, and 112 (98.2%) nurses and 103 (90.4%) families completed the follow-up evaluation. The total GDI score, which ranges from 54 to 378 with higher score indicating a better quality of death, was recorded as 299.81 ± 53.70 from the perspectives of nurses and 310.76 ± 49.55 from family members. The FAMCARE-2 score ranging from 17 to 85 with higher scores indicating greater satisfaction was 80.52 ± 8.75, with scores for symptom control, information support, family support, and patient psychological support at 23.73 ± 2.80, 18.87 ± 2.25, 18.94 ± 2.35, and 18.98 ± 1.95, respectively.

Conclusions

This study systematically implemented supportive care strategies tailored to the needs of patients and their families at the end of life through a hospital-based program and achieving satisfactory outcomes. The systematic approach and innovation of the program are worthy of further promotion.
目的中国癌症患者临终关怀的质量仍然不理想,特别是在他们生命的最后几天和几个小时,迫切需要改善。本研究旨在制定并实施以医院为基础的质量改善(QI)计划,为晚期癌症患者提供支持性护理,以提高癌症患者的死亡质量和家属满意度。方法本项目主要包括三个阶段:制定循证实践标准和相关材料;开展分层培训并提供捆绑的支持性护理策略;实施质量监督。为癌症晚期患者及其家属提供的支持性护理包括30个捆绑策略,分为5个部分:识别和确认患者可能进入生命的最后几天,临终沟通,以患者为中心的支持性护理,以家庭为中心的支持性护理和对家庭的丧亲支持。采用“好死量表”(GDI)从主管护士和家属角度评估癌症患者的死亡质量,采用“晚期癌症护理家庭满意度-2”(FAMCARE-2)量表评估家庭满意度。结果在2023年5月至2024年8月期间,来自北京、南京和昆明5家医院的114例患者接受了支持性护理,112名护士(98.2%)和103名家庭(90.4%)完成了随访评价。总GDI评分范围为54 ~ 378分,评分越高死亡质量越好,护士角度为299.81±53.70分,家属角度为310.76±49.55分。FAMCARE-2评分(17 ~ 85分)为80.52±8.75分,得分越高满意度越高,其中症状控制、信息支持、家庭支持和患者心理支持得分分别为23.73±2.80分、18.87±2.25分、18.94±2.35分和18.98±1.95分。结论本研究通过医院为基础的项目,系统地实施了针对患者及其家属临终需求的支持性护理策略,并取得了满意的结果。方案的系统性和创新性值得进一步推广。
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引用次数: 0
Frailty profiles and symptomatic radiation pneumonitis in patients with lung cancer undergoing radiotherapy: A latent class analysis 接受放射治疗的肺癌患者的虚弱特征和症状性放射性肺炎:一项潜在分类分析
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2025-12-23 DOI: 10.1016/j.apjon.2025.100840
Jiang Zhang , Xijuan Zhao , Song Li , Jiawei Liao , Lu Xu , Yanyan Fei , Jiang Wu , Qiongyao Guan

Objective

This study aimed to identify distinct frailty subtypes and their influencing factors, and to further explore the relationship between these frailty characteristics and the occurrence of symptomatic radiation pneumonitis (SRP) in patients with lung cancer undergoing radiotherapy.

Methods

The Observational study was conducted among 204 patients with lung cancer undergoing radical radiotherapy. Frailty was assessed via the Fried Frailty Phenotype, and nutritional risk was evaluated by the Nutrition Risk Screening 2002 (NRS-2002). Radiation pneumonitis (RP) was graded by the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 in conjunction with chest CT results. Radiotherapy parameters, including total radiation dose, treatment technique, bilateral lung mean dose (Dmean, Gy), and bilateral lung V20 (%), were collected. Latent class analysis (LCA) was performed to identify potential frailty subgroups. Multinomial logistic regression was conducted to determine factors associated with frailty classes, and binary logistic regression was subsequently used to assess the relationship between frailty class and the incidence of SRP in patients with lung cancer.

Results

LCA identified three distinct frailty subgroups: prefrailty (C1, 37.3%), frail physical activity decline (C2, 31.9%), and severe-frail core-strength decline (C3, 30.9%) group. Radiotherapy sessions, nutritional risk, and age were the main factors influencing frailty classification. The incidence of SRP in group C3 (68.3%) was significantly higher than that in group C2 (47.7%) and group C1 (19.7%) (P < 0.001). The risk of SRP was 3.71 times higher in C2 and 8.84 times higher in C3 as compared to C1.

Conclusions

Frailty among patients with lung cancer undergoing radiotherapy exhibit marked frailty heterogeneity. Those with severe frailty, particularly characterized by core strength and physical function decline, strongly associated with increased SRP risk. These findings indicating the importance of individualized nursing assessments and early, targeted interventions to prevent and mitigate frailty progression and SRP occurrence.

Trial registration

National Clinical Trial Registry (ChiCTR2400081213).
目的鉴别肺癌放疗患者不同的衰弱亚型及其影响因素,并进一步探讨这些衰弱特征与症状性放射性肺炎(SRP)发生的关系。方法对204例接受根治性放疗的肺癌患者进行观察性研究。脆弱性通过油炸脆弱表型进行评估,营养风险通过营养风险筛查2002 (NRS-2002)进行评估。放射性肺炎(RP)按照不良事件通用术语标准(CTCAE) 5.0版结合胸部CT结果进行分级。收集放疗参数,包括总放射剂量、治疗方法、双侧肺平均剂量(Dmean, Gy)、双侧肺V20(%)。进行潜在分类分析(LCA)以确定潜在的脆弱亚组。采用多项logistic回归确定与衰弱等级相关的因素,随后采用二元logistic回归评估肺癌患者衰弱等级与SRP发生率之间的关系。结果slca鉴定出三个不同的虚弱亚组:虚弱(C1, 37.3%)、虚弱体力活动下降(C2, 31.9%)和严重虚弱核心力量下降(C3, 30.9%)组。放疗时间、营养风险和年龄是影响衰弱分型的主要因素。C3组SRP发生率(68.3%)明显高于C2组(47.7%)和C1组(19.7%)(P < 0.001)。与C1相比,C2和C3发生SRP的风险分别高出3.71倍和8.84倍。结论肺癌放疗患者虚弱表现出明显的异质性。那些严重虚弱的人,尤其是核心力量和身体功能下降的人,与SRP风险增加密切相关。这些发现表明个性化护理评估和早期有针对性的干预措施对于预防和减轻虚弱进展和SRP发生的重要性。国家临床试验注册中心(ChiCTR2400081213)。
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引用次数: 0
Managing psychological distress in women with breast cancer: A systematic review of intervention trends in the past decade 管理女性乳腺癌患者的心理困扰:过去十年干预趋势的系统回顾
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2025-12-02 DOI: 10.1016/j.apjon.2025.100826
Haejeong An , Yoonjung Kim

Objective

The rising incidence and survival rates of breast cancer have increased the number of breast cancer survivors (BCSs) experiencing psychological distress that often overlaps with anxiety, depression, and fear of recurrence. Many existing interventions neglect the unique psychosocial contexts of BCSs, and unclear definitions of distress hinder consistent assessment and management. This systematic review evaluated recent interventions targeting psychological distress in BCSs and offers evidence-based insights.

Methods

Following PRISMA guidelines, six databases were searched for randomized controlled trials on distress interventions for BCSs published between 2014 and July 2025. Study quality was evaluated using Cochrane's RoB 2 tool, and data on intervention characteristics, outcomes, and measurement instruments were extracted.

Results

Fourteen randomized control trials involving 2447 BCSs were included. Among them, 8 (57%) report significant reductions, with six showing immediate post-intervention effects and two demonstrating effects only at follow-up (effect sizes ranged from small to large, Cohen's d = 0.44–1.54). Effective interventions included mindfulness-based approaches, virtual reality-integrated psychotherapy, and cognitive-behavioral therapy combined with hypnosis. In contrast, cognitive-focused interventions lacking experiential components and minimally structured digital programs showed non-significant results.

Conclusions

Effective distress management requires multimodal, theory-based interventions delivered by trained professionals, rather than cognitive-focused or minimally structured approaches. Future interventions should incorporate standardized distress assessment tools and clearly articulated theoretical frameworks, focusing on younger survivors, who remain significantly underrepresented. Although digital platforms enhance accessibility, their effectiveness depends on evidence-based content and structured implementation. Strengthening these elements will improve both the comparability and overall effectiveness of interventions for BCSs.
目的随着乳腺癌发病率和生存率的上升,越来越多的乳腺癌幸存者(BCSs)经历着焦虑、抑郁和害怕复发的心理困扰。许多现有的干预措施忽视了bcs独特的社会心理环境,并且不明确的痛苦定义阻碍了一致的评估和管理。本系统综述评估了最近针对bcs心理困扰的干预措施,并提供了基于证据的见解。方法根据PRISMA指南,检索2014年至2025年7月间发表的6个数据库中关于BCSs窘迫干预的随机对照试验。使用Cochrane的RoB 2工具评估研究质量,并提取有关干预特征、结果和测量工具的数据。结果纳入14项随机对照试验,共纳入2447例bcs。其中8例(57%)报告显著降低,6例显示干预后即刻效果,2例仅在随访中显示效果(效应大小从小到大,Cohen’s d = 0.44-1.54)。有效的干预包括基于正念的方法、虚拟现实综合心理治疗和认知行为疗法结合催眠。相比之下,缺乏经验成分的以认知为中心的干预和最低结构的数字程序显示出不显著的结果。结论有效的痛苦管理需要由训练有素的专业人员提供多模式、基于理论的干预,而不是以认知为中心或最低结构的方法。未来的干预措施应纳入标准化的痛苦评估工具和明确阐述的理论框架,重点关注仍然严重不足的年轻幸存者。尽管数字平台提高了可访问性,但其有效性取决于基于证据的内容和结构化的实施。加强这些要素将提高bcs干预措施的可比性和总体有效性。
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引用次数: 0
The burdens, coping strategies, and unmet needs of family caregivers of Chinese patients with lymphoma receiving commercial CAR-T-cell therapy: A qualitative study 中国淋巴瘤患者接受商业化car - t细胞治疗的家庭照顾者负担、应对策略和未满足需求:一项定性研究
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2026-01-06 DOI: 10.1016/j.apjon.2025.100850
Xijun Lin , Jiali Liu , Jianwen Chen , Jiamin Tang, Zhicong Huang, Ye Wang, Simei Shi

Objective

This study aimed to describe the caregiving experiences, coping strategies, and unmet health care needs of family caregivers supporting Chinese patients with large B-cell lymphoma receiving commercial chimeric antigen receptor T-cell therapy.

Methods

A qualitative descriptive design was adopted. Semistructured interviews were conducted with 19 primary family caregivers at a university-affiliated cancer centre in southern China. Data were analysed using Braun and Clarke's thematic analysis framework.

Results

Three themes were identified: (1) overwhelming caregiving burden, including financial strain, emotional distress, and role conflict; (2) caregivers' patient-centred coping strategies, including familial financial sacrifice, emotional suppression to protect the patient, and reprioritizing work and personal life for care; and (3) unmet caregiver support needs, including navigating therapy costs without systemic support, gaps in caregiver education and care coordination, and caregivers' emotional support being overlooked in care systems.

Conclusions

Family caregivers of patients receiving this therapy in China experience significant challenges, which are often managed through culturally influenced coping strategies amid limited formal support. A caregiver-inclusive approach (including financial reforms, tailored caregiver education, increased care coordination, and psychosocial services) is essential to support the well-being of family caregivers and optimize treatment outcomes amid evolving oncology trends in China.
目的探讨中国大b细胞淋巴瘤患者接受商业嵌合抗原受体t细胞治疗的家庭照护者的护理经验、应对策略和未满足的医疗需求。方法采用定性描述设计。在中国南方的一所大学附属癌症中心,对19名主要家庭照顾者进行了半结构化访谈。数据分析采用Braun和Clarke的主题分析框架。结果发现了三个主题:(1)照顾负担过重,包括经济压力、情绪困扰和角色冲突;(2)护理人员以患者为中心的应对策略,包括家庭经济牺牲、情绪抑制以保护患者、工作和个人生活优先于护理;(3)未满足的照顾者支持需求,包括在没有系统支持的情况下导航治疗费用,照顾者教育和护理协调的差距,以及照顾者在护理系统中被忽视的情感支持。结论:在中国,接受这种治疗的患者的家庭照顾者面临着巨大的挑战,这些挑战通常是通过受文化影响的应对策略来应对的,而正式的支持有限。在中国不断发展的肿瘤学趋势中,照顾者包容性方法(包括金融改革、量身定制的照顾者教育、加强护理协调和社会心理服务)对于支持家庭照顾者的福祉和优化治疗结果至关重要。
{"title":"The burdens, coping strategies, and unmet needs of family caregivers of Chinese patients with lymphoma receiving commercial CAR-T-cell therapy: A qualitative study","authors":"Xijun Lin ,&nbsp;Jiali Liu ,&nbsp;Jianwen Chen ,&nbsp;Jiamin Tang,&nbsp;Zhicong Huang,&nbsp;Ye Wang,&nbsp;Simei Shi","doi":"10.1016/j.apjon.2025.100850","DOIUrl":"10.1016/j.apjon.2025.100850","url":null,"abstract":"<div><h3>Objective</h3><div>This study aimed to describe the caregiving experiences, coping strategies, and unmet health care needs of family caregivers supporting Chinese patients with large B-cell lymphoma receiving commercial chimeric antigen receptor T-cell therapy.</div></div><div><h3>Methods</h3><div>A qualitative descriptive design was adopted. Semistructured interviews were conducted with 19 primary family caregivers at a university-affiliated cancer centre in southern China. Data were analysed using Braun and Clarke's thematic analysis framework.</div></div><div><h3>Results</h3><div>Three themes were identified: (1) overwhelming caregiving burden, including financial strain, emotional distress, and role conflict; (2) caregivers' patient-centred coping strategies, including familial financial sacrifice, emotional suppression to protect the patient, and reprioritizing work and personal life for care; and (3) unmet caregiver support needs, including navigating therapy costs without systemic support, gaps in caregiver education and care coordination, and caregivers' emotional support being overlooked in care systems.</div></div><div><h3>Conclusions</h3><div>Family caregivers of patients receiving this therapy in China experience significant challenges, which are often managed through culturally influenced coping strategies amid limited formal support. A caregiver-inclusive approach (including financial reforms, tailored caregiver education, increased care coordination, and psychosocial services) is essential to support the well-being of family caregivers and optimize treatment outcomes amid evolving oncology trends in China.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100850"},"PeriodicalIF":2.8,"publicationDate":"2026-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146073777","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Patient-reported outcomes with a personalized follow-up program after lung cancer resection: A single-center randomized controlled trial 肺癌切除术后患者报告的个性化随访结果:一项单中心随机对照试验
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2026-01-02 DOI: 10.1016/j.apjon.2025.100844
Yiqing Luo , Yuna Cheng , Zuodong Song , Hui Chen , Yinping Bo , Haobo Shixing

Objective

This study aims to determine the impact of PROM with a personalized follow-up program on the evaluation of quality of life and self-management for patients after lung cancer resection.

Methods

Given a formal power calculation a total of 240 patients with lung cancer. Participants were randomly assigned to either the experimental or the control groups. Patients in the experimental group received a personalized follow-up program of patient-reported outcomes. The control group received only the telephone follow-up. Baseline data (T0) were collected before the intervention (on the day of discharge), and quality of life, self-efficacy, and compliance were measured at 2 weeks (T1), 4 weeks (T2), and 4 months (T3) post-discharge.

Results

The difference in quality of life between the experimental and control groups was significant (Wald χ2 = 5.204, P = 0.023), with the experimental group showing significantly better quality of life at T2 compared to the control group (t = 2.515, P = 0.013). Both groups showed improvements in quality of life at all post-test time points (Wald χ2 = 574.167, P < 0.001), and the interaction between group and time was not statistically significant (Wald χ2 = 2.354, P = 0.308). Regarding self-management efficacy, Generalized Estimating Equations results indicated a significant difference between the experimental and control groups (Wald χ2 = 6.573, P = 0.010), with the experimental group showing significantly higher self-management efficacy at T2 and T3 compared to the control group (t = 3.024, P = 0.003; t = 2.214, P = 0.028). No significant differences were observed at T0 and T1. Both groups showed improvements in self-management efficacy at all post-test time points (Wald χ2 = 301.390, P < 0.001), and the interaction between group and time was not statistically significant (Wald χ2 = 3.971, P = 0.137).

Conclusions

For patients after lung cancer surgery, the program has optimized the evaluation of postoperative quality of life and self-management efficacy.

Trial registration

Chinese Clinical Trial Registry (NCT06483295).
目的本研究旨在通过个性化随访方案确定早膜PROM对肺癌切除术后患者生活质量评价和自我管理的影响。方法对240例肺癌患者进行正式功率计算。参与者被随机分配到实验组和对照组。实验组的患者接受了个性化的随访计划,根据患者报告的结果进行随访。对照组只接受电话随访。在干预前(出院当天)收集基线数据(T0),并在出院后2周(T1)、4周(T2)和4个月(T3)测量患者的生活质量、自我效能感和依从性。结果实验组与对照组患者生存质量比较差异有统计学意义(Wald χ2 = 5.204, P = 0.023),其中实验组患者T2期生存质量显著优于对照组(t = 2.515, P = 0.013)。两组患者在测试后各时间点的生活质量均有改善(Wald χ2 = 574.167, P < 0.001),组与时间的交互作用无统计学意义(Wald χ2 = 2.354, P = 0.308)。在自我管理效能方面,广义估计方程结果显示实验组与对照组之间存在显著差异(Wald χ2 = 6.573, P = 0.010),实验组在T2和T3时的自我管理效能显著高于对照组(t = 3.024, P = 0.003; t = 2.214, P = 0.028)。T0和T1无显著差异。两组患者在所有测试后时间点的自我管理效能均有改善(Wald χ2 = 301.390, P < 0.001),组与时间的交互作用无统计学意义(Wald χ2 = 3.971, P = 0.137)。结论该方案对肺癌术后患者的术后生活质量和自我管理效能进行了优化评价。中国临床试验注册中心(NCT06483295)。
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引用次数: 0
Latent profiles and influencing factors of sense of coherence in patients with advanced cancer: A cross-sectional study 晚期癌症患者连贯感的潜在特征及其影响因素:一项横断面研究
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2025-12-30 DOI: 10.1016/j.apjon.2025.100848
Yongqi Huang , Huimin Xiong , Xia Tian , Jinjia Lai , Liqun Zhou , Lili Chen , Wenli Xiao

Objective

This study aims to identify the latent profiles of sense of coherence (SOC) in patients with advanced cancer and explore its influencing factors encompassing sociodemographic and clinical characteristics, and generalized resistance resources (GRRs).

Methods

A cross-sectional study of 262 patients with advanced cancer was conducted by convenience sampling in Guangzhou, China, from September 2023 to July 2024. Data were collected including sociodemographic and clinical characteristics, SOC-13, Revised Life Orientation Test (LOT-R), Rosenberg Self-Esteem Scale (RSES), Inner Peace State Scale (IPSS), Gratitude Questionnaire-6 (GQ-6), and Social Support Rating Scale (SSRS). Statistical analysis was performed using latent profile analysis (LPA) and multivariate logistic regression analysis.

Results

Three latent profiles of SOC were identified: low SOC and low comprehensibility group (29.01%), moderate SOC and high meaningfulness group (40.08%), and high SOC and high manageability group (30.91%). This study found that SOC was impacted by self-perceived severity of the disease and GRRs including optimism, self-esteem, and inner peace (P < 0.05).

Conclusions

SOC in patients with advanced cancer exhibited different characteristics. Enhancing positive disease perception and GRRs including optimism, self-esteem, and inner peace may be effective strategies for improving their SOC. Healthcare professionals can formulate strategies such as tailored health education, symptom management, and positive psychological interventions to enhance SOC in patients with advanced cancer.
目的了解晚期癌症患者的连贯性感(SOC)潜在特征,并探讨其影响因素,包括社会人口学特征、临床特征和广义耐药资源(GRRs)。方法对2023年9月至2024年7月在中国广州进行的262例晚期癌症患者进行方便抽样的横断面研究。收集的数据包括社会人口学和临床特征、SOC-13、修订生活取向测试(LOT-R)、Rosenberg自尊量表(RSES)、内心平静状态量表(IPSS)、感恩问卷-6 (GQ-6)和社会支持评定量表(SSRS)。统计学分析采用潜型分析(LPA)和多因素logistic回归分析。结果鉴定出低SOC和低可理解性组(29.01%)、中等SOC和高意义性组(40.08%)和高SOC和高可管理性组(30.91%)3种SOC潜在特征。本研究发现,SOC受自我感知疾病严重程度和grr(乐观、自尊、内心平静)的影响(P < 0.05)。结论晚期肿瘤患者的soc表现出不同的特点。提高积极的疾病认知和grr(包括乐观、自尊和内心平静)可能是改善患者SOC的有效策略。医护人员可以制定策略,例如针对性的健康教育、症状管理和积极的心理干预,以提高晚期癌症患者的SOC。
{"title":"Latent profiles and influencing factors of sense of coherence in patients with advanced cancer: A cross-sectional study","authors":"Yongqi Huang ,&nbsp;Huimin Xiong ,&nbsp;Xia Tian ,&nbsp;Jinjia Lai ,&nbsp;Liqun Zhou ,&nbsp;Lili Chen ,&nbsp;Wenli Xiao","doi":"10.1016/j.apjon.2025.100848","DOIUrl":"10.1016/j.apjon.2025.100848","url":null,"abstract":"<div><h3>Objective</h3><div>This study aims to identify the latent profiles of sense of coherence (SOC) in patients with advanced cancer and explore its influencing factors encompassing sociodemographic and clinical characteristics, and generalized resistance resources (GRRs).</div></div><div><h3>Methods</h3><div>A cross-sectional study of 262 patients with advanced cancer was conducted by convenience sampling in Guangzhou, China, from September 2023 to July 2024. Data were collected including sociodemographic and clinical characteristics, SOC-13, Revised Life Orientation Test (LOT-R), Rosenberg Self-Esteem Scale (RSES), Inner Peace State Scale (IPSS), Gratitude Questionnaire-6 (GQ-6), and Social Support Rating Scale (SSRS). Statistical analysis was performed using latent profile analysis (LPA) and multivariate logistic regression analysis.</div></div><div><h3>Results</h3><div>Three latent profiles of SOC were identified: low SOC and low comprehensibility group (29.01%), moderate SOC and high meaningfulness group (40.08%), and high SOC and high manageability group (30.91%). This study found that SOC was impacted by self-perceived severity of the disease and GRRs including optimism, self-esteem, and inner peace (<em>P</em> &lt; 0.05).</div></div><div><h3>Conclusions</h3><div>SOC in patients with advanced cancer exhibited different characteristics. Enhancing positive disease perception and GRRs including optimism, self-esteem, and inner peace may be effective strategies for improving their SOC. Healthcare professionals can formulate strategies such as tailored health education, symptom management, and positive psychological interventions to enhance SOC in patients with advanced cancer.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100848"},"PeriodicalIF":2.8,"publicationDate":"2026-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023370","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stigma experiences among young and middle-aged testicular cancer survivors in China: A phenomenological study 中国中青年睾丸癌幸存者的耻辱感经历:现象学研究
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2025-12-02 DOI: 10.1016/j.apjon.2025.100825
Yu Zhao , Dan Li , Meng Zhang , Wei Yan , Hong Shen , Miaomiao Xu , Yuxin Liu

Objective

To explore the lived experiences and core structures of stigma among young and middle-aged Chinese testicular cancer (TC) survivors using a phenomenological approach.

Methods

A qualitative phenomenological study was conducted with 15 TC survivors aged 18–45 years, purposively recruited from a tertiary hospital in Beijing. In-depth semi-structured interviews were conducted, with data collection continuing until thematic saturation was reached. All interviews were audio-recorded, transcribed verbatim, and analyzed using Colaizzi's seven-step method to extract significant statements, formulate meanings, and generate themes.

Results

Four overarching themes and 11 subthemes emerged, situated within a social–ecological framework. (1) Internalized and Embodied Stigma (Individual Level): Shame-driven self-blame, hypervigilance toward bodily changes, and intergenerational transmission of stigma. (2) Relational Diplomacy and “Face” Management (Interpersonal Level): The ambivalence of family secrecy, strategic management of social capital, and contraction of social networks. (3) System-Driven Stigma (Community/Institutional Level): Cultural moralization of illness, clinical interactions inadvertently reinforcing stigma, and structural discrimination or neglect. (4) Confucian Ideology of the Body (Societal/Cultural Level): Moral weight of perceived lineage disruption and cultural expectations of bodily integrity.

Conclusions

Stigma among young and middle-aged Chinese TC survivors is pervasive and shaped by the interplay of biological vulnerability, Confucian moral values, and institutional structures. A comprehensive, culturally grounded, multi-level stigma-reduction strategy—spanning the individual, family, community, and health care system—is urgently needed to support psychosocial adaptation and improve survivorship outcomes.
目的用现象学方法探讨中国中青年睾丸癌(TC)幸存者的生活经历和耻辱感的核心结构。方法从北京某三级医院择取15例年龄在18 ~ 45岁的TC幸存者进行定性现象学研究。进行了深入的半结构化访谈,继续收集数据,直到达到主题饱和。所有的访谈都被录音,逐字抄写,并使用Colaizzi的七步法进行分析,以提取重要的陈述,形成意义,并产生主题。结果:在社会生态框架内,出现了4个总体主题和11个副主题。(1)内化与具身污耻感(个体层面):羞耻感驱动的自责、对身体变化的过度警惕和污耻感的代际传递。(2)关系外交与“面子”管理(人际层面):家庭保密的矛盾心理、社会资本的战略管理和社会网络的收缩。(3)系统驱动的病耻感(社区/机构层面):疾病的文化道德化、无意中强化病耻感的临床互动以及结构性歧视或忽视。(4)儒家的身体意识形态(社会/文化层面):对世系断裂的认知和对身体完整性的文化期望的道德权重。结论:在中国中青年TC幸存者中,耻辱感普遍存在,并受到生物脆弱性、儒家道德价值观和制度结构的相互影响。迫切需要一个全面的、以文化为基础的、多层次的减少耻辱感的策略——跨越个人、家庭、社区和卫生保健系统——以支持社会心理适应和改善生存结果。
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引用次数: 0
Association between postoperative urinary incontinence severity and anxiety in patients with prostate cancer: A chain mediation analysis of ehealth literacy and pelvic floor muscle training adherence 前列腺癌患者术后尿失禁严重程度与焦虑之间的关系:电子健康素养和骨盆底肌肉训练依从性的连锁中介分析
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2025-12-23 DOI: 10.1016/j.apjon.2025.100842
Qiuxia Qin, Juan Liu, Duo Zhang, Yuming Zhang, Xiaoqin Xie, Fan Yang, Lihong Huang, Xiaoqin Chen

Objective

This study aimed to examine the chain mediating roles of eHealth literacy and pelvic floor muscle training (PFMT) adherence in the association between urinary incontinence (UI) severity and anxiety.

Methods

A cross-sectional study was conducted using convenience sampling to recruit 240 patients with prostate cancer one month after surgery. Validated instruments were used to assess PFMT adherence (PFMT Adherence Scale), eHealth literacy (eHEALS), UI severity (International Consultation on Incontinence Questionnaire-Short Form), and anxiety (Generalized Anxiety Disorder-7). Structural equation modeling (SEM) was performed using AMOS 24.0 to evaluate direct and indirect effects. Mediation effects were tested using bias-corrected bootstrap analyses with 5000 resamples and 95% CI.

Results

At one month postoperatively, 45.05% of patients experienced anxiety, 60.40% reported moderate-to-severe urinary incontinence, and 71.78% demonstrated low eHealth literacy. High adherence to PFMT was observed in only 36.63% of participants. UI severity was indirectly associated with anxiety through three pathways: eHealth literacy (β = 0.154, P < 0.01), PFMT adherence (β = −0.047, P < 0.05), and a sequential pathway involving both eHealth literacy and PFMT adherence (β = 0.038, P < 0.01). eHealth literacy accounted for 22.3% of the total effect, PFMT adherence for 6.8%, and their combined chain mediation effect for 5.5%.

Conclusions

Urinary incontinence severity one month after prostate cancer surgery is a significant predictor of anxiety, exerting both direct and indirect effects. eHealth literacy and PFMT adherence function as important psychological and behavioral mediators, together explaining 34.6% of the total effect. Interventions aimed at enhancing eHealth literacy and promoting structured pelvic floor muscle training may help reduce postoperative anxiety and support recovery in this population.
目的本研究旨在探讨电子健康素养和骨盆底肌肉训练(PFMT)依从性在尿失禁(UI)严重程度与焦虑之间的连锁中介作用。方法采用方便抽样方法,对240例前列腺癌术后1个月患者进行横断面研究。使用经过验证的工具来评估PFMT依从性(PFMT依从性量表)、电子健康素养(eHEALS)、尿失禁严重程度(国际失禁咨询问卷-短表)和焦虑(广泛性焦虑症-7)。采用AMOS 24.0进行结构方程建模(SEM),评价直接和间接影响。采用偏差校正的自举分析对5000个样本和95% CI进行了中介效应检验。结果术后1个月,45.05%的患者出现焦虑,60.40%的患者出现中重度尿失禁,71.78%的患者出现低电子健康素养。只有36.63%的参与者观察到PFMT的高依从性。UI严重程度通过三条途径与焦虑间接相关:电子健康素养(β = 0.154, P < 0.01), PFMT依从性(β = - 0.047, P < 0.05),以及涉及电子健康素养和PFMT依从性的顺序途径(β = 0.038, P < 0.01)。电子健康素养占总效应的22.3%,PFMT依从性占6.8%,其联合连锁中介效应占5.5%。结论前列腺癌术后1个月尿失禁严重程度是焦虑的重要预测因子,有直接和间接影响。电子健康素养和PFMT依从性是重要的心理和行为中介,共同解释了34.6%的总效应。旨在提高电子健康素养和促进结构化盆底肌肉训练的干预措施可能有助于减少这一人群的术后焦虑和支持康复。
{"title":"Association between postoperative urinary incontinence severity and anxiety in patients with prostate cancer: A chain mediation analysis of ehealth literacy and pelvic floor muscle training adherence","authors":"Qiuxia Qin,&nbsp;Juan Liu,&nbsp;Duo Zhang,&nbsp;Yuming Zhang,&nbsp;Xiaoqin Xie,&nbsp;Fan Yang,&nbsp;Lihong Huang,&nbsp;Xiaoqin Chen","doi":"10.1016/j.apjon.2025.100842","DOIUrl":"10.1016/j.apjon.2025.100842","url":null,"abstract":"<div><h3>Objective</h3><div>This study aimed to examine the chain mediating roles of eHealth literacy and pelvic floor muscle training (PFMT) adherence in the association between urinary incontinence (UI) severity and anxiety.</div></div><div><h3>Methods</h3><div>A cross-sectional study was conducted using convenience sampling to recruit 240 patients with prostate cancer one month after surgery. Validated instruments were used to assess PFMT adherence (PFMT Adherence Scale), eHealth literacy (eHEALS), UI severity (International Consultation on Incontinence Questionnaire-Short Form), and anxiety (Generalized Anxiety Disorder-7). Structural equation modeling (SEM) was performed using AMOS 24.0 to evaluate direct and indirect effects. Mediation effects were tested using bias-corrected bootstrap analyses with 5000 resamples and 95% CI.</div></div><div><h3>Results</h3><div>At one month postoperatively, 45.05% of patients experienced anxiety, 60.40% reported moderate-to-severe urinary incontinence, and 71.78% demonstrated low eHealth literacy. High adherence to PFMT was observed in only 36.63% of participants. UI severity was indirectly associated with anxiety through three pathways: eHealth literacy (<em>β</em> = 0.154, <em>P</em> &lt; 0.01), PFMT adherence (<em>β</em> = −0.047, <em>P</em> &lt; 0.05), and a sequential pathway involving both eHealth literacy and PFMT adherence (<em>β</em> = 0.038, <em>P</em> &lt; 0.01). eHealth literacy accounted for 22.3% of the total effect, PFMT adherence for 6.8%, and their combined chain mediation effect for 5.5%.</div></div><div><h3>Conclusions</h3><div>Urinary incontinence severity one month after prostate cancer surgery is a significant predictor of anxiety, exerting both direct and indirect effects. eHealth literacy and PFMT adherence function as important psychological and behavioral mediators, together explaining 34.6% of the total effect. Interventions aimed at enhancing eHealth literacy and promoting structured pelvic floor muscle training may help reduce postoperative anxiety and support recovery in this population.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100842"},"PeriodicalIF":2.8,"publicationDate":"2026-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145973883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Determinants of patient delay and its association with quality of life among young women with breast cancer in China: A cross-sectional study 中国年轻女性乳腺癌患者延迟的决定因素及其与生活质量的关系:一项横断面研究
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2026-01-06 DOI: 10.1016/j.apjon.2025.100846
Yueyang Peng , Jun Ma , Li Liu , Jinnan Xiao , Can Gu

Objective

The incidence of breast cancer in young women (< 40 years old) has been increasing in recent years. Patient delay is significant to disease prognosis, thus early diagnosis and prompt effective therapy represent the key elements in controlling breast cancer. This study aimed to identify determinants of patient delay and assess the association of patient delay with quality of life (QoL).

Methods

A cross-sectional study was conducted among 286 young patients with breast cancer from October, 2022 to March, 2023 at four tertiary hospitals in Hunan province, China with the guidance of Andersen Behavioral Model of Health Services Utilization. Determinants of patient delay were identified using binary logistic regression analysis. The association between patient delay and QoL was analyzed using linear regression.

Results

A total of 106 (37.06%) young patients with breast cancer had experienced patient delay, indicating that more than one in three women faced this critical barrier to timely care. Patients who lived in countryside (odd ratio [OR] 3.676, 95% confidence interval [CI] 1.468–9.206), had an initial outpatient consultation to other department (OR 3.910, 95% CI 1.439–10.624), waited > 7-day for initial outpatient consultation (OR 11.350, 95% CI 3.450–37.345) were more likely to experience patient delay. Detecting disease at routine physical examination (OR 0.208, 95% CI 0.045–0.967), having higher critical health literacy (OR 0.676, 95% CI 0.506–0.904), and having more friend support (OR 0.921, 95% CI 0.855–0.993), patients were less likely to experience patient delay. Patient delay was negatively correlated with QoL including overall FACT-B (t = −2.443, P = 0.015), physical well-being (t = −3.526, P < 0.001), functional well-being (t = −2.077, P = 0.039), and additional concerns (t = −1.974, P = 0.049).

Conclusions

Waiting time for initial outpatient consultation > 7-day was the strongest determinant of patient delay among young women with breast cancer. Other significant factors included rural residence and initial consultation in non-specialist departments, while higher health literacy, friend support, and detection via physical examination were protective. Patient delay was significantly associated with poorer QoL, particularly in the domains of physical well-being, functional well-being, and additional concerns. These findings underscore the need for interventions targeting health care access to reduce patient delay and improve patient health outcomes.
目的近年来,年轻女性(40岁)乳腺癌的发病率呈上升趋势。患者延迟对疾病预后有重要影响,早期诊断和及时有效治疗是控制乳腺癌的关键因素。本研究旨在确定患者延迟的决定因素,并评估患者延迟与生活质量(QoL)的关系。方法以Andersen卫生服务利用行为模型为指导,对2022年10月至2023年3月湖南省四所三级医院286例年轻乳腺癌患者进行横断面研究。使用二元逻辑回归分析确定患者延误的决定因素。采用线性回归分析患者延迟与生活质量之间的关系。结果共有106例(37.06%)年轻乳腺癌患者经历过患者延误,表明超过三分之一的女性面临这一及时护理的关键障碍。居住在农村的患者(奇比[OR] 3.676, 95%可信区间[CI] 1.468 ~ 9.206),首次门诊到其他科室就诊(OR 3.910, 95% CI 1.439 ~ 10.624),首次门诊等待7天(OR 11.350, 95% CI 3.450 ~ 37.345)更容易出现患者延误。在常规体检中发现疾病(OR 0.208, 95% CI 0.045-0.967),具有较高的关键健康素养(OR 0.676, 95% CI 0.506-0.904),以及有更多的朋友支持(OR 0.921, 95% CI 0.855-0.993),患者不太可能经历患者延迟。患者延迟与生活质量呈负相关,包括总体FACT-B (t = - 2.443, P = 0.015)、身体健康(t = - 3.526, P = 0.001)、功能健康(t = - 2.077, P = 0.039)和其他问题(t = - 1.974, P = 0.049)。结论初诊等待时间(7天)是年轻女性乳腺癌患者延迟就诊的最大决定因素。其他重要因素包括农村居住和在非专科部门的初步咨询,而较高的健康素养、朋友支持和通过体检发现是保护因素。患者延迟与较差的生活质量显著相关,特别是在身体健康、功能健康和其他问题方面。这些发现强调需要针对卫生保健可及性采取干预措施,以减少患者延误并改善患者健康结果。
{"title":"Determinants of patient delay and its association with quality of life among young women with breast cancer in China: A cross-sectional study","authors":"Yueyang Peng ,&nbsp;Jun Ma ,&nbsp;Li Liu ,&nbsp;Jinnan Xiao ,&nbsp;Can Gu","doi":"10.1016/j.apjon.2025.100846","DOIUrl":"10.1016/j.apjon.2025.100846","url":null,"abstract":"<div><h3>Objective</h3><div>The incidence of breast cancer in young women (&lt; 40 years old) has been increasing in recent years. Patient delay is significant to disease prognosis, thus early diagnosis and prompt effective therapy represent the key elements in controlling breast cancer. This study aimed to identify determinants of patient delay and assess the association of patient delay with quality of life (QoL).</div></div><div><h3>Methods</h3><div>A cross-sectional study was conducted among 286 young patients with breast cancer from October, 2022 to March, 2023 at four tertiary hospitals in Hunan province, China with the guidance of Andersen Behavioral Model of Health Services Utilization. Determinants of patient delay were identified using binary logistic regression analysis. The association between patient delay and QoL was analyzed using linear regression.</div></div><div><h3>Results</h3><div>A total of 106 (37.06%) young patients with breast cancer had experienced patient delay, indicating that more than one in three women faced this critical barrier to timely care. Patients who lived in countryside (odd ratio [OR] 3.676, 95% confidence interval [CI] 1.468–9.206), had an initial outpatient consultation to other department (OR 3.910, 95% CI 1.439–10.624), waited &gt; 7-day for initial outpatient consultation (OR 11.350, 95% CI 3.450–37.345) were more likely to experience patient delay. Detecting disease at routine physical examination (OR 0.208, 95% CI 0.045–0.967), having higher critical health literacy (OR 0.676, 95% CI 0.506–0.904), and having more friend support (OR 0.921, 95% CI 0.855–0.993), patients were less likely to experience patient delay. Patient delay was negatively correlated with QoL including overall FACT-B (<em>t</em> = −2.443, <em>P</em> = 0.015), physical well-being (<em>t</em> = −3.526, <em>P &lt;</em> 0.001), functional well-being (<em>t</em> = −2.077, <em>P</em> = 0.039), and additional concerns (<em>t</em> = −1.974, <em>P</em> = 0.049).</div></div><div><h3>Conclusions</h3><div>Waiting time for initial outpatient consultation &gt; 7-day was the strongest determinant of patient delay among young women with breast cancer. Other significant factors included rural residence and initial consultation in non-specialist departments, while higher health literacy, friend support, and detection via physical examination were protective. Patient delay was significantly associated with poorer QoL, particularly in the domains of physical well-being, functional well-being, and additional concerns. These findings underscore the need for interventions targeting health care access to reduce patient delay and improve patient health outcomes.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100846"},"PeriodicalIF":2.8,"publicationDate":"2026-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146073955","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Adaptation and psychometric validation of the Turkish version of the motivation for healing scale in patients with cancer 土耳其版癌症患者治疗动机量表的适应和心理计量学验证
IF 2.8 3区 医学 Q1 NURSING Pub Date : 2026-12-01 Epub Date: 2025-12-23 DOI: 10.1016/j.apjon.2025.100841
Özkan Uğuz , Gülseren Keskin

Objective

The Motivation for Healing Scale (MHS) is a valid and reliable instrument for assessing the motivation for healing in patients with cancer. This methodological study aimed to translate the MHS into Turkish and evaluate the validity and reliability of the Turkish version (T-MHS).

Methods

The study sample consisted of 320 oncology patients selected using convenience sampling method. The T-MHS was assessed for face, content, construct, and convergent validity, as well as internal consistency and test-retest reliability. Face validity was evaluated by patients, content validity was evaluated using the Content Validity Index (CVI), and construct validity was evaluated using Confirmatory Factor Analysis (CFA). Convergent validity was examined by correlating the T-MHS scores with illness uncertainty and hope. Reliability was determined using Cronbach's alpha and test-retest method. Statistical analyses were performed using IBM SPSS Statistics (version 30.0) and AMOS (version 26.0).

Results

The mean patient age was 52.99 ± 13.50 years. The T-MHS demonstrated strong content validity (CVI = 0.98) and high internal consistency (Cronbach's α = 0.87). Test-retest analysis confirmed good stability over time. CFA supported the original five-factor structure and showed excellent model fit. Convergent validity was confirmed by a positive correlation with hope (r = 0.57, P < 0.001) and a negative correlation with illness uncertainty (r = −0.62, P < 0.001).

Conclusions

The T-MHS is a reliable and valid instrument for the clinical assessment of patients with cancer and for research aimed at interventions that enhance motivation for healing in this population.
目的采用愈合动机量表(MHS)评估癌症患者的愈合动机,是一种有效、可靠的工具。本方法学研究旨在将MHS翻译成土耳其语,并评估土耳其语版本(T-MHS)的效度和信度。方法采用方便抽样法抽取320例肿瘤患者作为研究样本。评估T-MHS的面效度、内容效度、结构效度和收敛效度,以及内部一致性和重测信度。面部效度由患者评估,内容效度采用内容效度指数(CVI)评估,结构效度采用验证性因子分析(CFA)评估。通过将T-MHS得分与疾病不确定性和希望相关联来检验收敛效度。信度采用Cronbach’s alpha法和重测法测定。采用IBM SPSS Statistics(30.0版本)和AMOS(26.0版本)进行统计分析。结果患者平均年龄为52.99±13.50岁。T-MHS具有较强的内容效度(CVI = 0.98)和较高的内部一致性(Cronbach’s α = 0.87)。反复测试分析证实了良好的稳定性。CFA支持原始的五因子结构,模型拟合良好。收敛效度与希望呈正相关(r = 0.57, P < 0.001),与疾病不确定性负相关(r = - 0.62, P < 0.001)。结论T-MHS是一种可靠和有效的癌症患者临床评估和研究干预措施的工具,旨在提高这一人群的治疗动机。
{"title":"Adaptation and psychometric validation of the Turkish version of the motivation for healing scale in patients with cancer","authors":"Özkan Uğuz ,&nbsp;Gülseren Keskin","doi":"10.1016/j.apjon.2025.100841","DOIUrl":"10.1016/j.apjon.2025.100841","url":null,"abstract":"<div><h3>Objective</h3><div>The Motivation for Healing Scale (MHS) is a valid and reliable instrument for assessing the motivation for healing in patients with cancer. This methodological study aimed to translate the MHS into Turkish and evaluate the validity and reliability of the Turkish version (T-MHS).</div></div><div><h3>Methods</h3><div>The study sample consisted of 320 oncology patients selected using convenience sampling method. The T-MHS was assessed for face, content, construct, and convergent validity, as well as internal consistency and test-retest reliability. Face validity was evaluated by patients, content validity was evaluated using the Content Validity Index (CVI), and construct validity was evaluated using Confirmatory Factor Analysis (CFA). Convergent validity was examined by correlating the T-MHS scores with illness uncertainty and hope. Reliability was determined using Cronbach's alpha and test-retest method. Statistical analyses were performed using IBM SPSS Statistics (version 30.0) and AMOS (version 26.0).</div></div><div><h3>Results</h3><div>The mean patient age was 52.99 ± 13.50 years. The T-MHS demonstrated strong content validity (CVI = 0.98) and high internal consistency (Cronbach's <em>α</em> = 0.87). Test-retest analysis confirmed good stability over time. CFA supported the original five-factor structure and showed excellent model fit. Convergent validity was confirmed by a positive correlation with hope (<em>r</em> = 0.57, <em>P</em> &lt; 0.001) and a negative correlation with illness uncertainty (<em>r</em> = −0.62, <em>P</em> &lt; 0.001).</div></div><div><h3>Conclusions</h3><div>The T-MHS is a reliable and valid instrument for the clinical assessment of patients with cancer and for research aimed at interventions that enhance motivation for healing in this population.</div></div>","PeriodicalId":8569,"journal":{"name":"Asia-Pacific Journal of Oncology Nursing","volume":"13 ","pages":"Article 100841"},"PeriodicalIF":2.8,"publicationDate":"2026-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145973884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Asia-Pacific Journal of Oncology Nursing
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