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As the main undertakers of home care for urostomy patients after discharge, family caregivers play an important role in patients' postoperative recovery. Family caregivers of patients with urostomy may be under greater pressure than patients themselves, and there is a heavy burden on caregivers, and their care needs are complicated and urgent. However, there is a lack of research on the care needs of family caregivers of bladder cancer patients with urostomy, and tools to assess the specific needs of family caregivers of bladder cancer patients with urostomy are lacking. This study aimed to develop an assessment tool to measure the specific needs of family caregivers for bladder cancer patients with urinary ostomies and to examine its reliability and validity. The development of the scale is based on the Supportive Care Framework, and the item pool is determined through literature retrieval and qualitative research. The items of the scale were revised via Delphi expert consultation, and 198 family caregivers of urostomy patients in five 3 A hospitals in Taiyuan City, China, were investigated. SPSS 26.0 and AMOS 22.0 were used for data analysis. Exploratory factor analysis and confirmatory factor analysis were carried out to evaluate the reliability, content validity, discrimination validity, structure validity, and convergence validity of the scale. Exploratory factor analysis identified three dimensions of the 21-item scale of care needs of family caregivers of patients with bladder cancer undergoing urostomy, namely, demand for disease information, demand for physical and mental comfort, and demand for social support. Cronbach's α coefficient and half-reliability of the whole scale and each dimension are greater than 0.7, indicating high internal consistency. Confirmatory factor analysis shows that the scale fits the data well, and the content validity, discrimination validity, and convergence validity of the scale are excellent, which provides evidence of support. The scale developed by the authors is a relatively reliable and effective tool for evaluating the specific care needs of family caregivers of patients with bladder cancer undergoing urostomy. Future research could develop role-specific subscales tailored to distinct kinship categories (e.g., spouses, daughters, sons) to enable precision assessment of caregiving needs.
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http://dx.doi.org/10.1038/s41598-025-12678-0 | DOI Listing |
Alzheimers Dement
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Multiomics Investigation of Neurodegenerative Diseases (MIND) Lab, Montréal, Québec, Canada.
Living with dementia requires decision making about numerous topics including daily activities and advance care planning (ACP). Both individuals living with dementia and care partners require informed support for decision making. We conducted an umbrella review to assess knowledge translation (KT) interventions supporting decision making for individuals living with dementia and their informal care partners.
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Université Laval, faculté des sciences infirmières, Pavillon Ferdinand-Vandry, 1050 avenue de la Médecine, local 3645, G1V 0A6, Québec, Canada. Electronic address:
"Cultural Safety, a decolonizing approach critical of the research conceptual frameworks and of care practices in nursing, has enjoyed since its emergence in the 1990s a growing success in New Zealand, Australia and Canada. Being reworked and adapted to new contexts, its political dimension however loses its importance, raising concerns about Cultural Safety's potential for systemic transformation and the fight against health inequalities affecting Indigenous peoples. At the heart of this debate lies the question of "culture" as a means of patient emancipation vis-à-vis the norms of the dominant society and the expertise of caregivers, a debate we seek to clarify in this article.
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September 2025
Association Soins aux professionnels de la santé, 31 avenue de Versailles, 75016 Paris, France.
Quality of care, attractiveness of the healthcare professions, embodiment of prevention messages: these are all issues linked to the health of caregivers. In response to the many alarming observations made, the association Soins aux professionnels de la santé (SPS) has been playing a central role for ten years, offering psychological support and prevention initiatives. Through its initiatives, SPS defends a strong conviction: preserving the health of caregivers, to improve the lives of all.
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Clinique Mon Repos, 11 chemin de la Vernique, 69130 Écully, France. Electronic address:
The psychological suffering of healthcare professionals is often summed up as burn-out, but we need to think more broadly about compassion fatigue, secondary trauma and vicarious trauma, which are more characteristic of the care professions. This particular clinic makes specific support necessary through, among other things, dedicated units to facilitate access to care for healthcare professionals and target support to their needs. To this end, since 2018 we have been offering a transdiagnostic care program, based on processual therapy.
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Plateforme professionnelle addiction Occitanie, 11 rue des Novars, 31300 Toulouse, France. Electronic address:
Healthcare professionals face major psychosocial risks (burn-out, addictions, exhaustion). Despite their commitment to caring for others, they find it hard to ask for help. In France, access to healthcare for caregivers remains inadequate.
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