Thematische Bibliographien / Client-centered care

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Auswahl der wissenschaftlichen Literatur zum Thema „Client-centered care“

Autor: Grafiati

Veröffentlicht am 30. Juni 2021

Zuletzt aktualisiert am 28. Januar 2023

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Zeitschriftenartikel zum Thema "Client-centered care"

Schoot, Tineke, Ireen Proot, Marja Legius, Ruud ter Meulen und Luc de Witte. „Client-Centered Home Care“. Clinical Nursing Research 15, Nr. 4 (November 2006): 231–54. http://dx.doi.org/10.1177/1054773806291845.

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Alvarez, Carrol. „Client Empowerment: Is it Always Client-Centered Care?“ Clinical Nurse Specialist 11, Nr. 3 (Mai 1997): 95. http://dx.doi.org/10.1097/00002800-199705000-00003.

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Kyler, Panelpha (Penny) L. „Client-Centered and Family-Centered Care: Refinement of the Concepts“. Occupational Therapy in Mental Health 24, Nr. 2 (26.05.2008): 100–120. http://dx.doi.org/10.1080/01642120802055150.

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Evans, Dawn, Annmarie Kinsella und Cynthia Love-Williams. „Wellness begins at home: Client-centered care“. Journal of Interprofessional Education & Practice 1, Nr. 2 (Juni 2015): 57–58. http://dx.doi.org/10.1016/j.xjep.2015.07.025.

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Fontein-Kuipers, Yvonne, Elise van Beeck, Liesbeth Kammeraat und Fleur Rutten. „The Woman-Centeredness of Various Dutch Maternity Service Providers During Antenatal and Postnatal Care“. International Journal of Childbirth 9, Nr. 2 (01.06.2019): 92–101. http://dx.doi.org/10.1891/2156-5287.9.2.92.

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AIMSTo examine the woman-centeredness of maternity care providers from the woman's perspective. To investigate the validity and reliability of the Client Centered Care Questionnaire among a childbearing population.DESIGNA cross-sectional study.METHODSThe self-report Client Centered Care Questionnaire was administered to evaluate women's one-on-one antenatal and postnatal care appointments with various Dutch care providers: community and hospital-based midwives, General Practitioners, (registrar) obstetricians, sonographers, and maternity care nurses.RESULTSEight-hundred and fifteen completed questionnaires were received. Exploratory and confirmatory factor analyses provided support for a two-factor model, with an acceptable model fit. Woman-centeredness of all maternity care providers showed scores above baseline for the neutral value. Welch ANOVA showed a statistical significant effect of the type of maternity care practitioner in providing woman-centered care during antenatal and postnatal visits (F(5.8) = 7.79). The Bonferroni post hoc test showed that women assigned significantly higher woman-centered care scores to community-based midwives compared with hospital-based midwives (p .011) and compared with registrars/obstetricians (p < .001).CONCLUSIONAlthough overall scores of perceived woman-centeredness indicated a good to excellent performance of woman-centered care, with significantly higher scores for community-based midwives, it cannot be assumed that current woman-centered care completely meets the needs of Dutch childbearing women. The Client Centered Care Questionnaire (CCCQ) is an adequate instrument to measure woman-centered care in antenatal and postnatal maternity services. Further research regarding measuring woman-centered care is needed.

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Kanji, Noureen, Jason B. Coe, Cindy L. Adams und Jane R. Shaw. „Effect of veterinarian-client-patient interactions on client adherence to dentistry and surgery recommendations in companion-animal practice“. Journal of the American Veterinary Medical Association 240, Nr. 4 (15.02.2012): 427–36. http://dx.doi.org/10.2460/javma.2400.4.427.

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Objective—To explore the relationship between veterinarian-client-patient interactions and client adherence to dental and surgery recommendations and to test the a priori hypotheses that appointment-specific client satisfaction and relationship-centered care are positively associated with client adherence. Design—Cross-sectional study. Sample—A subsample of 19 companion-animal veterinarians and 83 clients from a larger observational study consisting of 20 randomly recruited veterinarians and a convenience sample of 350 clients from eastern Ontario. Procedures—Videotaped veterinarian-client-patient interactions containing a dentistry recommendation, surgery recommendation, or both were selected for inclusion from the larger sample of interactions coded with the Roter interaction analysis system. Client adherence was measured by evaluating each patient's medical record approximately 6 months after the videotaped interaction. The clarity of the recommendation, appointment-specific client-satisfaction score, and relationship-centered care score were compared between adhering and nonadhering clients. Results—Among the 83 veterinarian-client-patient interactions, 25 (30%) clients adhered to a dentistry recommendation, surgery recommendation, or both. The odds for adherence were 7 times as great for clients who received a clear recommendation, compared with clients who received an ambiguous recommendation from their veterinarian. Moreover, adhering clients were significantly more satisfied as measured after the interview. Interactions resulting in client adherence also had higher scores for relationship-centered care than did interactions leading to nonadherence. Conclusions and Clinical Relevance—Veterinarian use of a relationship-centered care approach, characterized as a collaborative partnership between a veterinarian and a client with provision of clear recommendations and effective communication of the rationale for the recommendations, has positive implications for client adherence.

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Nuriaty Masdiputri, Rr Sri, Yanti Yanti und Asri Hidayat. „Student’s Comprehension About Philosiphy of Maternity Care “Women Centered Care” Based on the Report of Continuity of Care (COC)“. Journal of Midwifery 4, Nr. 2 (07.06.2020): 60. http://dx.doi.org/10.25077/jom.4.2.60-67.2019.

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Background: Mortality in Indonesia has significantly increased. Students’ comprehension about maternity care “woman centered care” philosophy is an important thing in high quality maternity care, it is one solution to decrease the number of mortality rate. Continuity of care maternal clinic model of learning (PKK-CoC) is giving for student to learn the philosophy.Objectives: reveals level and form of students’ comprehension about maternity care “woman centered care” philosophy.Method: Mixed method with sequential explanatory strategy. The quatitative are use analitic descriptive design, while the quantitative use case study design. Population and sample is 55 students of Estu Utomo Boyolali institute health and science who have taken PKK-CoC. Sampling use criterion and intensity.Result: qualitatively, students overall comprehension is good. Quantitatively, students comprehension on personalized care, holistic care, collaborative care, and evidence based care is also good. Partnership care is the only aspect considered in effective.Conclusion: continuity of care shows that client and family are in good heatlth, zero mortality rate, client fells safe and comfortable, and client has correct and fast care. It is also found that students’ confidence, skills, and comprehension about maternity care “woman centered care” philosophy are increased. It is suggested including the PKK-CoC model into curriculum of midwifery education

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KOLS, ADRIENNE J., JILL E. SHERMAN und PHYLLIS TILSON PIOTROW. „Ethical Foundations of Client-Centered Care in Family Planning“. Journal of Women's Health 8, Nr. 3 (April 1999): 303–12. http://dx.doi.org/10.1089/jwh.1999.8.303.

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Ross, Anita, Nicole Roberts und Lauren Morton. „Perceptions of Paraprofessionals Following Trainings in Providing Client-Centered Care“. American Journal of Occupational Therapy 74, Nr. 4_Supplement_1 (01.08.2020): 7411505244p1. http://dx.doi.org/10.5014/ajot.2020.74s1-po9208.

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Bamm, Elena L., Peter Rosenbaum, Seanne Wilkins, Paul Stratford und Nadilein Mahlberg. „Exploring Client-Centered Care Experiences in In-Patient Rehabilitation Settings“. Global Qualitative Nursing Research 2 (15.04.2015): 233339361558203. http://dx.doi.org/10.1177/2333393615582036.

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Dissertationen zum Thema "Client-centered care"

Wambugu, Peniel Mugo. „Client-Centered Care Approach to Group Home Care“. ScholarWorks, 2015. https://scholarworks.waldenu.edu/dissertations/1948.

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Scholars since the 19th century have focused on the provision of care in group homes and have demonstrated that structure (that is, the staff, facilities, and equipment), is critical in the delivery of care. The researchers, however, advocate doing for, rather than doing with the clients the activities that address the clients' welfare. The purpose of this study is to investigate how a client-centered approach would affect the quality of care delivered to the mentally challenged individuals (MCIs) in a group home. The study employed the quality-care framework in which the emphasis is on structure (skills), process (efficiency), and outcome (results). The research questions examined operational values underpinning company sanctioned work processes, how personal values underpin work processes of the direct caregivers, configuration of personal values the caregivers believe should be supported in the group home context, and how critical incidents shaped the value set of direct caregivers in regard to care processes. Using structured questionnaires and observing staff as they delivered care to their clients, data were collected from participants who were direct caregivers (n = 7), a facility administrator, and a nurse. The data were coded, categorized, and analyzed for emergent themes. The results of the analysis indicated that there was discord between staff and the organizational leadership. This discord could be improved through increased interaction between the mentioned stakeholders. The results further depicted that client-centered care may have a positive impact on the health of the MCIs that would enable the MCIs to make notable contributions to social change.

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Eriksson, Anna, und Helene Lindqvist. „Att möjliggöra aktivitet och delaktighet till livets slut“. Thesis, Luleå tekniska universitet, Institutionen för hälsovetenskap, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-79080.

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Syfte: Syftet med denna studie var att beskriva arbetsterapeuters erfarenheter inom specialiserad palliativ vård. Metod: En kvalitativ studie genomfördes. Deltagarna bestod av elva arbetsterapeuter yrkesverksamma inom specialiserad palliativ vård. Datainsamlingen skedde med semistrukturerade intervjuer per telefon och datan analyserades med en kvalitativ innehållsanalys. Resultat: Analysen resulterade i ett övergripande tema; Att möjliggöra aktivitet och delaktighet till livets slut med tre kategorier; Flexibilitet och följsamhet, Interventioner med livskvalité som mål och Teamet fyller flera funktioner. Resultatet visar att arbetsterapeuternas erfarenheter är att samtal och följsamhet utgör grunden för den terapeutiska relation som behövs för att stödja klienten i sin process och genomföra interventioner som bygger på klientens egna behov och önskemål. Resultatet visar att det krävs framförhållning och flexibilitet eftersom det sker snabba förändringar hos klienterna. Interventioner som utförs syftar till att klienten skall uppleva livskvalité till livets slut vilket bland annat görs med kompensatoriska åtgärder, handledning, anpassning av aktiviteter och miljö samt symtomlindring. Att arbeta i ett multiprofessionellt team utgör grunden för att möta klientens fysiska, psykiska, sociala och existentiella behov där teamet även utgör ett emotionellt och kunskapsmässigt stöd för arbetsterapeuten. Slutsats: Resultatet kan bidra med förståelse och kunskap för det förhållningssätt och arbetssätt som arbetsterapeuten använder sig av inom palliativ vård för att möta klientens behov och möjliggöra aktivitet och delaktighet till livets slut. Studien kan även bidra till en förståelse för betydelsen av ett fungerande teamarbete, samt varför arbetsterapeuten som profession inom de palliativa teamen behövs. Ytterligare forskning behövs för att beskriva arbetsterapeutens unika kompetens i den palliativa vården samt hur den kompetensen förvärvas. Vidare behövs forskning om arbetsterapi inom olika palliativa vårdformer för att belysa och tydliggöra arbetsterapi inom palliativ vård och skapa en gemensam teoretisk grund.
Aim: The aim of this study was to describe occupational therapists’ experiences of specialized palliative care. Method: A qualitative study was conducted. The participants consisted of eleven occupational therapists working in specialized palliative care. The data collection was conducted with semi-structured interviews using telephone and the data was analyzed with a qualitative content analysis. Result: The analysis resulted in an overall theme; To enable occupation and participation until the end of life with three categories; Flexibility and compliance, The goal of interventions is quality of life, The multifunctional team. The result shows that the occupational therapists experiences is that conversation and compliance form the basis of the therapeutic relationship required to support clients in their process and implement interventions based on the clients individual needs and requests. The result shows that it takes foresight and flexibility to meet the clients rapid changes. The aim with interventions is that clients shall experience quality of life till the end of life. This is for instance made with compensatory interventions, guidance, adapting activities and environment and symptomatic relief. Working in a multi-professional team is the basis for meeting the client's physical, mental, social and existential needs, where the team also stands for knowledge exchange and as an emotional support. Conclusion: The result can contribute with understanding and knowledge of the approach and working method used by the occupational therapist in palliative care to meet the client's needs and enable activity and participation towards the end of life. The study can also contribute to an understanding of the importance of teamwork in palliative care and why the occupational therapist is needed in the palliative care teams. Further research is needed on the occupational therapists unique competence and how it is acquired. Further research is needed on occupational therapy in various palliative care forms to clarify occupational therapy in palliative care and to create a common theoretical basis.

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Nilsson, Elin, und Olivia Stenmark. „Arbetsterapeutisk hemrehabilitering för personer som drabbats av stroke med fokus på klientcentrering : En litteraturöversikt“. Thesis, Luleå tekniska universitet, Institutionen för hälsa, lärande och teknik, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-86144.

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Syftet med litteraturöversikten var att beskriva kunskapsläget vad gäller arbetsterapeutiskt hemrehabilitering vid stroke med fokus på klientcentrering. Metoden som använts under litteraturöversiktens gång bygger på 10 artiklar hämtade från fyra databaser inriktade på arbetsterapi och rehabilitering; PubMed, CINAHL, AMED och PsycINFO. Författarna har granskat de valda artiklarna, identifierat likheter och skillnader i resultatet som resulterade i tre kategorier. Resultatets kategorier blev; Hemmiljöns betydelse för den klientcentrerade rehabiliteringen, klientens delaktighet under den klientcentrerade hemrehabiliteringen och det sociala nätverkets påverkan på den klientcentrerade hemrehabiliteringen. Resultatet visar på att hemmiljön vid rehabilitering efter stroke har stor betydelse för klienten och den fortsatta rehabiliteringen i hemmet. Klientens delaktighet vid rehabiliteringen är viktig för att rehabiliteringen ska bli så bra som möjligt och för att få effektiva resultat. Anhöriga och andra personer runt klienten är viktiga för rehabiliteringen efter stroke. Slutsatsen som författarna kom fram till var att det behövs rutiner för att trygga klienter vid hemrehabilitering. Utbildning och information till anhöriga måste säkerställas. Klienters känsla av delaktighet i rehabiliteringen behöver stärkas. Ytterligare forskning på hemrehabilitering och klientcentrering i samband med stroke behövs.

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Azevedo, Maria Manuela Gonçalves de. „O cuidado de si: A relação de ajuda promotora de qualidade de vida dos enfermeiros“. Master's thesis, Instituto Superior de Psicologia Aplicada, 2008. http://hdl.handle.net/10400.12/327.

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O objectivo deste estudo qualitativo foi compreender a experiência vivida dos enfermeiros no âmbito da prestação de cuidados na comunidade e identificar estratégias promotoras de saúde deste grupo profissional, e a partir delas descrever a estrutura de uma relação de ajuda na perspectiva dos enfermeiros. A amostra, intencional de voluntários, foi constituída por 7 enfermeiros, a quem, através de entrevista não estruturada, foi pedida a descrição de situações da sua prática profissional percebidas como impulsionadoras de uma relação de ajuda. Utilizando-se o método de análise fenomenológica de Giorgi (1985, 1997, 2000) salientaram-se nos resultados dois temas major: "penosidade do exercício profissional" e "significações de relação de ajuda", enquadrando-se neste último as dimensões "relação de ajuda/relação aidante dirigida aos utentes" e "relação de ajuda dirigida aos enfermeiros". Estes temas permitiram aceder a uma maior compreensão do significado de uma relação de ajuda construída no espaço do encontro enfermeiro-utente e no espaço da relação com os pares e outros profissionais, enraizando-se o significado da sua importância e utilidade na penosidade do exercício profissional dos enfermeiros, relacionada com as condições de trabalho e a organização do trabalho. A descrição estrutural de uma relação de ajuda - como estratégia promotora de saúde e qualidade de vida dos enfermeiros - parece apontar no sentido de a relação de ajuda estar intimamente ligada com a comunicação, caracterizada através da atitude de escuta activa e da possibilidade de expressão e de partilha de emoções e sentimentos no seio de um espaço privilegiado, o da equipa de pares ou da equipa multiprofissional, funcionando como grupo de suporte ou de auto-ajuda.

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Nogueira, Susana Maria Correia Coelho. „Aconselhamento psicológico como experiência de crescimento em direcção à maturidade: Uma proposta de clarificação do desafio de Carl Rogers“. Master's thesis, Instituto Superior de Psicologia Aplicada, 2006. http://hdl.handle.net/10400.12/735.

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Dissertação de Mestrado em Relação de Ajuda
Rogers é o percursor da intervenção na área do aconselhamento psicológico e define o papel do conselheiro como um facilitador do crescimento e desenvolvimento pessoal com vista à maior independência e integração dos clientes. Nesta conceptualização do aconselhamento, é o conjunto das atitudes do conselheiro que permite ao cliente uma experiência de crescimento em direcção à maturidade. É este o desafio de Carl Rogers. Os objectivos fundamentais deste trabalho são fazer uma reflexão sobre o aconselhamento psicológico, apresentando uma proposta de definição para alguns dos conceitos utilizados na prática de aconselhamento centrado na pessoa, facilitando a definição clara dos constructos teóricos subjacentes a esta actividade pouco estabelecida entre nós; e apresentar os resultados de um questionário aplicado a 80 sujeitos, 37 psicólogos e 43 com formação superior noutra área, com o objectivo de caracterizar o aconselhamento psicológico e o conselheiro e avaliar a existência de diferenças entre estes grupos. Os resultados deste questionário oferecem pistas para a definição deste campo de intervenção psicológica, não evidenciando diferenças entre os grupos.

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Lu, Ying-Yu, und 盧盈妤. „Evaluation of Quality of Care in Home Services from Client-Centered Perspective: Example of Nantou County“. Thesis, 2011. http://ndltd.ncl.edu.tw/handle/68888393937981583381.

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碩士
國立暨南國際大學
社會政策與社會工作學系
100
The aim of the study was to investigate the related factors of the quality of care in home services from client-centered perspectives, and to understand the impacts of the users, caregivers, providers, and care workforces on the quality of care in home care services. This study used quantitative method by using face-to-face surveys to collect data to understand the perceptions of the quality of care in home services from users and caregivers of nine agencies in Nantou County. A total of 302 users’ samples used home services completed questionnaires, and from the users’ samples to match that 167 care workforces samples are completed the questionnaires. The researcher also combined qualitative method by using in-depth interview, including 4 users, 4 care workforces, and 4 supervisors of those agencies. The main findings of this research are as following: 1. The quality of care in home services was affected by users, caregivers, care workforces, and agencies. From the Quality of Care Scale, the factors of the relationships between home care clients and their workers had the highest score. In the second place was the factor of the skillfulness of home care, and in the third place was the factor of the homecare in being responsive to client expectations. The result indicates the relationships between home care clients and their workers are the most important factor of quality of care in home services. 2. From the quantitative data, by the hierarchical regression analysis, the significant variables of quality of care in home services are the characteristics of users, caregivers, and agencies, including total income, previous types of jobs, users’ subjective perception of the workforces, relationship, and organization established period. These variables are significant predictive factors of quality of care in home services. In depth analysis, all of the variables accounted for 29.3% of variances. The first sub-scale had the lowest explained variances of 25.0%.The second sub-scale had the highest explained variances of 35.3%, and the third sub-scale accounted for 31.7% variances. 3. In qualitative interviews, from the client perspectives, good care relationships appear to be important determinants of Quality of Care, including communication, appropriateness, and trust. "On time" and "Do not be late" are the most important facors that users are concerned for. The skillfulness of home care is the basic equipment, because the factor shows the professional attitudes of care workforces. However, if the care relationship is positive, the techniques which are poor may be acceptable. From the perspectives of the system, whether the needs assessment actually rendered service users also affect the demands for quality of care, and to respond to the needs of the expectations of the users. Therefore, even care relationship is great, when the needs are unmet or the assessment is incorrect, negative feelings still emerged. Finally, according to the finding and conclusions, this study has suggestions for further research on practice, academic, and policy.

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Hrdá, Karolína. „Péče zaměřená na člověka v domově pro seniory“. Master's thesis, 2016. http://www.nusl.cz/ntk/nusl-350676.

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The aim of this thesis is to identify and to describe barriers to the implementation of person-centered care in specific residential care facility for the elderly. For this purpose, the author firstly conceptualizes the concept of person-centered care. Consequently, she develops the Framework for conducting research. The theoretical portion consists of five chapters. The first chapter focuses on the person- centered care concept introduction, then it describes the relationship between concepts 'individualization of care' and 'person-centered care'. In the conclusion of the first chapter, the Schema of the concept is introduced. The Schema visualizes the structure for chapters two to five. In those chapters, a description of the systems defined in the Schema is provided. Those are: Care Recipients, Direct Care Actors, and Service Providers. The end of the first part brings the topic of a suitable organizational culture. The empirical portion firstly offers the summary of the theoretical background - so follows the Framework for the consequent analysis and data interpretation - then introduces relevant aspects within researched organization, particularly within organization currently implemented a psychobiographical model of care that is the approach to person-centered care. The empirical portion...

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Dentry, Terri Louise. „Seeing more than we saw before: the lived experience of interprofessional practice“. Thesis, 2021. https://vuir.vu.edu.au/42899/.

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This research provides an in-depth exploration of the experience of practitioners and clients utilising an interprofessional practice approach within a community health care setting with clients who have complex chronic care needs. An interprofessional approach has been demonstrated to have enhanced outcomes for clients who have complex chronic conditions. However, interprofessional practice approaches are not well defined in the literature. Therefore, understanding how practitioners and clients co-design healthcare using an interprofessional practice approach requires detailed research within particular healthcare settings. A focus on the management of clients from refugee and asylum seeker background with chronic pain offered a valuable context for this study. An interpretative phenomenological analysis (IPA) was chosen to support the participants' illumination of lived experience in their interactions with each other. Interviews were conducted with nine practitioners and nine clients. To determine the data's trustworthiness, journaling, member checking, external auditing, and reflexivity were used, all of which align with the IPA approach. The analysis revealed four themes within the practitioners’ experience and three themes within the clients’ experience. The first theme to emerge from the practitioner interviews, ‘My place within the team', illuminated that the interprofessional approach was a natural extension of the values within this community health setting. A strong team focus allowed most members to feel immersed in the interprofessional team. However, some practitioners felt aggrieved by those in the team who did not become as immersed as they did in the interprofessional activities. They demarcated these practitioners as being on the team's periphery. The second theme, 'Consolidating understanding', highlighted how an interprofessional approach initially caused some anxiety due to a fear of the unknown; however, with experience confidence was gained in the teams shared roles and mutual trust developed. The third theme, 'Coping with an interprofessional approach', highlighted areas of moral discomfort in the way practitioners reflected on their experience. This discomfort included coping with difficult conversations and using resistance as a protective mechanism. The impact of moral discomfort on the practitioners was reduced by the development of trust and respect which in turn led to the practitioner’s willingness to seek each other out for input into client care with an open approach. The fourth theme, 'Finding the balance for the client's benefit', highlighted the practitioner's concerns regarding the ethical and moral considerations of an interprofessional approach in this care setting, balanced with the approach's benefits compared to usual care. Analysis of the clients’ experience of an interprofessional approach was limited due to language barriers. However, three themes were revealed: 'The person behind the pain' that included feelings of uncertainty and holistic needs to be healed, 'Opening up to others' that included learning to put trust in a team, and 'Ready to move on' that separated clients into those who were now owing their pain and those who did not move forward. This study's findings provide useful information about the practical applications of interprofessional practice in a community health care setting that is deficient in the literature. The clinical implications relate to training and processes required to ensure effective interprofessional practice in this setting. The practitioners may have benefitted from additional training, particularly experiential training in applying an nterprofessional approach in practice. Tailored training to their care setting could help overcome the initial anxiety of the unknown and help prepare them for coping with difficult discussions in areas outside their professional practice.

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Moeketsi, Ramathabathe Rossy. „Exploring the involvement of children in the decisionmaking process about their future“. Diss., 2009. http://hdl.handle.net/10500/3397.

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The researcher wanted to explore the experiences of children who removal by a social worker either to an institution or to foster homes. The researcher wanted to find out if the behaviour of absconding could be explained by using systems theory, contructivism, cybernetics and person- centered theory. The researcher hypothesized that children abscond from alternative care as a means of communicating with the social worker involved as well as any other person significant in their lives. The study wanted to explore how these children perceived their involvement in the decision making process of their removal. The researcher only interviewed children who had absconded from the alternative care placements. The study found that all the children interviewed perceived that they were not involved in any way in the process of removal. They all saw their removal as a form of punishment for something they did wrong, but they did not get an opportunity to discuss with their parents or significant others. They also perceived their absconding as an effort to rectify the situation. A lot of anger and suspicion towards social workers was encountered during the study. In terms of the theories mentioned above, these perceptions are the children’s own reality, which might differ from the realities as created or perceived by social workers. It is hypothesized that social workers who use the Child Care Act 74/83 and its regulations in the removal of children, do it to protect the children from risky situations as their job responsibility requires. This study indicates that the children did not experience removal as protection. Instead of children feeling protected in the alternative care, they felt blamed, judged and unhappy about their removal and excluded from the process. The researcher made a few suggestions that could be considered when social workers removing children to alternative care. It is recommended that social workers involve the children and their parents or significant others in the entire process of deciding the future of any children in their (parents’) care. However, if removal is deemed necessary, just telling or informing children that they will be removed for their own safety is not enough. Children might not perceive the situation as dangerous. Instead, they might see the social worker as posing a danger to them and their families and thus try to shut the social worker and what s/he says out of their minds. Findings safe ways to involve children and families in the decisions about their future may require of social workers to revive their academically acquired knowledge in this respect.
Social Work
M.A. (Social Sciences (Mental Health))

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Wittstock, Luke Jonathan. „Wrestling heart : the autoethnographic faith journey of a developing psychologist“. Diss., 2019. http://hdl.handle.net/10500/25919.

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This autoethnography tells the story of my faith journey with a special focus on my years as a Catholic seminarian and the change towards embarking on a career as a clinical psychologist. Pertinent childhood experiences are also shared to contextualise my story. The narrative, “Wrestling Heart”, is the centre and the produced data of this autoethnography. As an “evocative” narrative, it independently seeks to fulfil many of the goals of an autoethnography, such as being therapeutic for both writer and readers, and imbuing culture with critical thinking. The sharing of the narrative is augmented with a thematic analysis of it and Carl Rogers’ Person-Centred Approach is mainly used to comprehend the gleaned themes. The movement towards a comprehension of my experience is consistent with the philosophical foundation of this study: phenomenology. It is envisaged that the utility of this study lies primarily in its interrogation of the relationship between religion and mental health, its in-depth depiction of an individual grappling with their faith in relation to mental health, and the way in which the writing of this autoethnography therapeutically fostered greater congruence for me the writer, as I prepare to work as a clinical psychologist.
Psychology
M.A. (Clinical Psychology)

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Bücher zum Thema "Client-centered care"

Client-centered care for clinical medical assisting. Clifton Park, NY: Thomson Delmar Learning, 2007.

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Client-centered exercise prescription. 2. Aufl. Champaign, IL: Human Kinetics, 2006.

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Client-centered exercise prescription. Champaign, IL: Human Kinetics, 1998.

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1940-, Fearing Virginia G., und Clark Jo 1958-, Hrsg. Individuals in context: A practical guide to client-centered practice. Thorofare, NJ: SLACK, 2000.

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Adams, Neal. Treatment planning for person-centered care: The road to mental health and addiction recovery : mapping the journey for individuals, families, and providers. Amsterdam: Elsevier Academic Press, 2005.

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Polatajko, Helene J., 1949- author und Canadian Association of Occupational Therapists, Hrsg. Enabling occupation II: Advancing an occupational therapy vision for health, well-being, & justice through occupation. Ottawa, Ontario: Canadian Association of Occupational Therapists, 2013.

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Prouty, Garry. Pre-therapy: Reaching contact-impaired clients. Ross-on-Wye [UK]: PCCS Books, 2002.

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Person-centered counselling and Christian spirituality: The secular and the holy. London: Whurr Publishers, 1998.

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Bryant-Jefferies, Richard. Counselling a recovering drug user: A person-centred dialogue. Abingdon: Radcliffe Medical Press, 2003.

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Person-centred counselling for people with dementia: Making sense of self. London: Jessica Kingsley Publishers, 2009.

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Mehr Quellen

Buchteile zum Thema "Client-centered care"

Zimring, Fred M., und Nathaniel J. Raskin. „Carl Rogers and client/person-centered therapy.“ In History of psychotherapy: A century of change., 629–56. Washington: American Psychological Association, 1992. http://dx.doi.org/10.1037/10110-018.

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Silani, Giorgia, Alberto Zucconi und Claus Lamm. „Carl Rogers Meets the Neurosciences: Insights from Social Neuroscience for Client-Centered Therapy“. In Interdisciplinary Handbook of the Person-Centered Approach, 63–78. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7141-7_5.

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Roberts, Pamela. „Development of a Client-Centered Occupational Performance Measure“. In 50 Studies Every Occupational Therapist Should Know, herausgegeben von Elizabeth A. Pyatak und Elissa S. Lee, 327–32. Oxford University PressNew York, 2023. http://dx.doi.org/10.1093/med/9780197630402.003.0047.

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Abstract The Canadian Occupational Performance Measure is a standardized outcome measure that assists in structuring and focusing the occupational therapy assessment, reassessment, and intervention process. Using a semi-structured interview with patients who have a wide range of diagnoses in various practice settings, the information gathered by the Canadian Occupational Performance Measure reflects the importance of the skill or activity to the client in the areas of self-care, productivity, and leisure. The Canadian Occupational Performance Measure is designed to assist the occupational therapist in establishing occupational performance goals based on client perceptions of need and measures the change in defined problem areas.

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„Client-centered care: Integrating the perspectives of childhood sexual abuse survivors and clinicians“. In Trauma and Physical Health, 177–215. Routledge, 2008. http://dx.doi.org/10.4324/9780203885017-13.

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„3. An Empowered Substance Abuse Service Delivery Process: Expanding the Client-Centered Continuum of Care“. In Substance Abuse Intervention, Prevention, Rehabilitation, and Systems Change, 135–306. Columbia University Press, 2001. http://dx.doi.org/10.7312/free10236-005.

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Anderson, Jane. „Health Coaching“. In Integrative Nursing, 171–84. Oxford University Press, 2014. http://dx.doi.org/10.1093/med/9780199860739.003.0014.

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Health coaching, an emerging health care specialty, is a way of being-knowing-doing that facilitates lifestyle change and well-being. Coaching is client-centered and based on values of partnership, empowerment, authenticity, trust, self-reflection and openness. Using strategies that include motivational interviewing, nonviolent communication, reflective practice and appreciative inquiry, health coaches accompany clients along their health-seeking journey. Developing professional competencies, including presencing, active listening, education, self-discovery and change processes, form the basis for new credentialing/certification processes and educational programs. These competencies align with the principles of integrative nursing and nursing’s historical focus on patient-centered, relationship-based care that facilitates body-mind-spirit health and well-being.

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Biesecker, Barbara B., Kathryn F. Peters und Robert Resta. „Psychological Counseling Theories“. In Advanced Genetic Counseling, 143–70. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780190626426.003.0009.

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Due to the diversity of clients’ needs, there is no central theory of genetic counseling. Psychological counseling offers an array of theories pertinent to the goals of genetic counseling sessions. These theories offer frameworks in which strategies emerge that may be most effective in meeting client needs. Person-centered theory was introduced at the origins of genetic counseling for its contribution of the concept of nondirectiveness. Yet Carl Rogers himself obliterated this from his person-centered theory once he came to appreciate that all human interactions have directive components. Since then, this theory has remained pertinent to genetic counseling because of its high regard for clients’ personal resources and their self-actualizing potential. Cognitive-behavioral and solution-focused theories can be applied to cases where decisions are being deliberated to help clients weigh potential consequences. Strength-based counseling leaves clients empowered to effectively cope with challenging circumstances. Such theories are contrasted to practical approaches that include bereavement and crisis counseling. In the latter, the counselor attends to clients’ need for safety and care from loved ones as they absorb devastating news.

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Kattari, Shanna K., Héctor Torres, Kim Fountain und Ing Swenson. „Providing Appropriate Health-Care Services to Transgender and Gender Nonconforming Survivors of IPV“. In Transgender Intimate Partner Violence, 169–201. NYU Press, 2020. http://dx.doi.org/10.18574/nyu/9781479830428.003.0007.

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Mental and medical health-care providers often serve as first responders and longer-term therapeutic support for transgender intimate partner violence (T-IPV) survivors. Mental health-care providers in particular are positioned to offer important, client-centered assistance in dealing with the intricacies of addressing IPV, and research finds they are among the most trusted and utilized sources of help by survivors. Likewise, due in part to the emergency medical needs of survivors of physical IPV, medical health-care providers can play a vital role in recognizing IPV victimization and guiding patients toward needed resources. Drawing on both the T-IPV and broader lesbian, gay, bisexual, transgender, and queer IPV literatures, this chapter provides a template for best practices in a multisystem approach with regard to developing culturally appropriate mental and medical health-care provider training programs, screening protocols, treatment modalities, and auxiliary service referrals when working with T-IPV survivor populations.

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Jordan, Katie. „Exploring the Association Between Therapy Time and Functional Recovery Through Mobility and Self Care Clinical Outcomes“. In 50 Studies Every Occupational Therapist Should Know, herausgegeben von Elizabeth A. Pyatak und Elissa S. Lee, 333–40. Oxford University PressNew York, 2023. http://dx.doi.org/10.1093/med/9780197630402.003.0048.

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Abstract With therapy minutes generally closely aligned with regulatory and reimbursement requirements, there is little room to consider patient characteristics, time (length of stay [LOS]), and clinical judgment in determining the most cost-effective and clinically optimal plan of care. This study provides valuable insight into client-centered variables (comorbidities, functional outcomes, burden of care) that bring meaning and perspective into determining a value-based rehabilitation plan rather than one based on arbitrary required and assigned minutes. In this study, patients are assigned to one of nine recovery groups following hip fracture surgery. Recovery groups are based on therapy minutes per LOS as low, medium, or high and functional gains in self-care and mobility as measured by the Functional Independence Measure as low, medium, or high. All groups are compared on LOS, providing insight into the role of clinical decision-making and consideration of patient characteristics in determining the dose and intensity of therapy services.

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Kelly, Laura. „Person-Centered Therapy: A Client With Postpartum Depression“. In Case Study Approach to Psychotherapy for Advanced Practice Psychiatric Nurses. New York, NY: Springer Publishing Company, 2020. http://dx.doi.org/10.1891/9780826195043.0003.

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Konferenzberichte zum Thema "Client-centered care"

Martinez, Clea, Marie-Laure Espinouse und Maria Di Mascolo. „Continuity of care in home services: a client-centered heuristic for the home health care routing and scheduling problem“. In 2018 5th International Conference on Control, Decision and Information Technologies (CoDIT). IEEE, 2018. http://dx.doi.org/10.1109/codit.2018.8394968.

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Battalova, Alfiya. „Disability Epistemology: Bridging the Gap Between Clinicians' Lived Experiences of Disability and Client-Centered Care“. In 2019 AERA Annual Meeting. Washington DC: AERA, 2019. http://dx.doi.org/10.3102/1436091.

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Macharia, Paul, David Katz, George Otieno, Monisha Sharma, Beatrice Wamuti, Harrison Lagat, Sarah Masyuko et al. „Implementing open data kit integrating barcode-based client identification in HIV testing and linkage to care: A user-centered design“. In 2021 IEEE International Humanitarian Technology Conference (IHTC). IEEE, 2021. http://dx.doi.org/10.1109/ihtc53077.2021.9698914.

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M. Yemelyanov, Alexander, Rahul Sukumaran und Alina Yemelyanov. „Application of ExpressDecision2 in User-Centered and Shared-with-Expert Decisions Under Risk and Uncertainty“. In 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1001812.

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ExpressDecision2 is a general-purpose web application designed to support the individual in making difficult decisions under uncertainty, which are emotionally driven and typically solved by using rational intuition. This web app is based on the self-regulation model of the thinking process developed within the framework of the systemic-structural activity theory. This paper demonstrates the application of two customized versions of ExpressDecision2: 1. ED2StatinChoice – for making a patient-centered and shared-with-clinician decision about taking statins for cholesterol reduction to prevent a heart attack or stroke. The two primary resources regarding taking statins for cholesterol reduction are The 2018 AHA/ACC Cholesterol Guideline and Mayo Clinic Statin Choice Decision-Aid tool. These and other guidelines and decision aids, as well as information derived from a health professional, provide the patient with essential information regarding the pros and cons of using statins, while also empowering the patient to make the ultimate decision regarding whether they should take statins. Overall, such a problem is both uncertain and difficult for the patient and so requires them to establish both short- and long-term goals, as well as relevant options for selection. ED2StatinChoice is designed specifically to help the patient make the best choice in such a difficult scenario. ED2StatinChoice complements existing decision-support tools, such as the Mayo Clinic Statin Choice Decision Aid. Its method of assistance involves clarifying the goal and various choices with subsequent aggregation of all pros and cons, thus helping make a motivated decision regarding which statin therapy is most preferable. 2. ED2InsuranceChoice – for making a client-centered and potentially shared-with-agent decision about buying an insurance policy in order to reduce financial uncertainty and make accidental loss more manageable. People buy health, car, life, home and other types of insurance to protect themselves from financial loss in the event of illness, car damage, house fire and other accidents, respectively. For example, they make decisions when choosing from among liability, comprehensive and collision insurance types. This decision-making process is guided by tangible statistical factors regarding people’s risks of accidental losses and by non-tangible factors, such as “peace of mind” due to being protected against financial loss in the event of an accident. It is important to note that peace of mind is an essential and decisive factor when selecting an insurance policy. It reflects subjective justification of rate adequacy for the premium: the premium should be reasonable and coverage must be sufficient. Unfortunately, such non-tangible factors as peace of mind from being protected against financial loss in an accident, as well as anxiety from losing money while paying an insurance premium for coverage that doesn’t get used unless you have an accident are not sufficiently reflected in existing models of insurance choice.

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Berichte der Organisationen zum Thema "Client-centered care"

Ndhlovu, Lewis. Quality of care and utilisation of MCH and FP services at Kenyan health facilities. Population Council, 1999. http://dx.doi.org/10.31899/rh1999.1017.

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Quality of services is playing an increasingly important role in many family planning (FP) programs. In 1995, a national Situation Analysis Study of 254 health facilities was conducted in Kenya to assess the status and quality of FP services in the country. An in-depth survey of a subsample of 28 health facilities was conducted the following year. From these facilities, 1,834 women were interviewed about their experiences with services at facilities when they sought antenatal, child health, and FP services. The goal of the survey was to examine the links between quality of care in FP services and contraceptive behavior. A key focus was directed at information and counseling as elements of service quality. Further, the subject of quality was explored in the context of how women switched facilities for the same and different services of antenatal care, child health, and FP. As noted in this report, this study highlights the gap that exists in the provision of quality reproductive health services. Despite the call for client-centered services, there is evidence that a wide gap still remains in providing relevant information to clients.

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A client-centered approach to reproductive health: A trainer's manual. Population Council, 2005. http://dx.doi.org/10.31899/rh16.1015.

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This training manual grew out of a project to improve the quality of care rendered by public-sector providers of reproductive health services. Implemented by the Population Council in collaboration with the Ministries of Population, Welfare, and Health, in Pakistan, the project extended beyond improving the quality of care provided by family planning workers and incorporated health workers who provided maternal and child health services. The success of all efforts made by the service delivery system in attracting and keeping clients depends upon the content and quality of interaction when the client comes in contact with the provider—whether the client is visiting a clinic or being visited by a community-based worker at home. To offer good quality of care, the provider should treat the client with dignity and respect, assess her reproductive health needs by asking questions rather than making assumptions based on her profile, and help her negotiate a solution appropriate to her circumstances. This training manual is oriented toward improving providers’ interpersonal skills. Emphasis is placed on the client and helping her meet her own needs rather than on meeting artificial goals or targets.

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Philippines and Senegal: Services improve quality of care but fail to increase FP continuation. Population Council, 2002. http://dx.doi.org/10.31899/rh2002.1016.

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In 1999, Frontiers in Reproductive Health collaborated on studies on the impact of interventions to improve quality of care in the Philippines and Senegal. The two interventions were part of a multicountry Population Council study (also undertaken in Pakistan and Zambia) to test whether improving quality affects women’s contraceptive continuation. The Philippines study focused on training in family planning (FP), supportive supervision, and refresher courses to improve client-provider interaction. The Senegal study compared the impact of improved quality of care at five newly established “reference centers” with five clinics that served as controls. Data were gathered through analyses of quality of care at all 10 sites in 1997, when the reference centers had begun implementation, and in 1998, 16 months later. As detailed in this brief, the introduction of client-centered service delivery with a focus on the client-provider interaction resulted in better quality of care at sites in the Philippines and Senegal. However, improving quality of care alone was not found to be sufficient to significantly increase the length of time women continued to use contraception.

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