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Academic literature on the topic 'Mentally ill Victoria Interviews'

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Published: 10 December 2022
Last updated: 29 January 2023

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Journal articles on the topic "Mentally ill Victoria Interviews"

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Perera, Carlyle, and Beth Wilson. "The treatment and care of mentally ill offenders in Victoria, Australia." Psychiatry, Psychology and Law 3, no. 1 (April 1996): 47–61. http://dx.doi.org/10.1080/13218719609524874.

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Ali, Shagufta Hamid, Altaf Ghanni Bhatti, and Abid Ghafoor Chaudhry. "Cultural Perception Regarding Mental Illness: A Case Study of Domestic Carers in Jalalpur Pirwala, District Multan." Global Social Sciences Review VI, no. III (September 29, 2021): 159–67. http://dx.doi.org/10.31703/gssr.2021(vi-iii).17.

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Culture guides the individuals to live their lives according to the beliefs set by the people of that culture. In order to know about the cause of any illness, the combination of knowledge and culture is considered to be a powerful tool. The study aimed to see the cultural perceptions about mental illness in Jalalpur Pirwala. This study focused on the carers of mentally ill persons by observing their perceptions regarding the mentally ill person of their families. The subject of the research was 18-60 years old mentally ill persons. Data collection methods included observation, unstructured interviews with practitioners (spiritual healers/bhoopa), and in-depth interviews were conducted with caretakers of mentally ill persons, selected through snowball sampling. Findings showed that cultural beliefs regarding mental illness are related to supernatural or divine phenomena in which causes of mental illness are Allah’s will or punishment, witching, black magic, evil eye, curse or women’s fault.
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Castle, David J. "Letter from Australia: mental healthcare in Victoria." Advances in Psychiatric Treatment 17, no. 1 (January 2011): 2–4. http://dx.doi.org/10.1192/apt.bp.110.008375.

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SummaryMental health services in the state of Victoria, Australia, have undergone enormous change over the past 15 years, with the closure of all stand-alone psychiatric hospitals and a shift of resources and services into the community. Although successful overall, various areas cause concern, including pressure on acute beds, a paucity of alternative residential options, and suboptimal integration of government and non-government agencies concerned with the care of people with mental illnesses. Certain groups, notably those with complex symptom sets such as substance use and mental illness, intellectual disability and forensic problems, remain poorly catered for by the system. Finally, community stigma and lack of work inclusion for mentally ill individuals are ongoing challenges.
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Becker, T., S. Kilian, R. Kilian, C. Lahmeyer, and S. Krumm. "Family Needs, Children and Parenthood in People with Mental Illness." European Psychiatry 24, S1 (January 2009): 1. http://dx.doi.org/10.1016/s0924-9338(09)70281-0.

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Objective:Given that parental mental diseases affect the whole family system, a family centered support and help system seems appropriate for families with a mentally ill mother/father. However, the majority of mental health services do not integrate interventions for the family system into psychiatric treatment programs.Aims:To introduce a counselling and support service for families with a mentally ill parent (FIPS) that has been established at a psychiatric hospital serving a large catchments area. Preliminary results of a qualitative study that focused on the clients’ family background as well as on their reasons for utilising the service and service satisfaction will be presented.Methods:Factors that impact the family system are considered and brought to a concept for counselling and support service for families with a mentally ill parent. Problem-focused interviews with 14 clients (mentally ill parents and relatives) of the counselling service for families were subjected to content analysis.Results:Most clients came to the counselling centre because of worries that the parent's mental illness might negatively affect children's well-being. Mentally ill mothers described their daily lives as utterly burdensome and also reported strong feelings of guilt towards their children. The concept of FIPS includes psychoeducation, social therapy, case management and family therapy. Clients assessed the counselling service as helpful and reported some significant changes.
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Redubla, RPm, Cristina Marie, and Ginbert Permejo Cuaton. "A PHENOMENOLOGICAL STUDY ON THE EXPERIENCES OF CARERS OF THE MENTALLY ILL ON A MENTAL HEALTH FACILITY IN THE PHILIPPINES." International Journal of Research -GRANTHAALAYAH 7, no. 3 (March 31, 2019): 38–47. http://dx.doi.org/10.29121/granthaalayah.v7.i3.2019.941.

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In the Philippines, mental illness remains a stigmatized, under-researched topic. Few studies on mental health are available, and at present, there is scant literature concerning the experiences of people living with and giving care to mentally ill peoples. This qualitative study aims to help families, mental health professionals, and the general community, gain an understanding of the experiences of caregivers and the challenges they face in sustaining their roles. Phenomenological method was employed for this research to explore the experiences of caregivers of the mentally ill patients in a Mental Health Facility in Leyte, Philippines. The primary data were collected through in-depth interviews with carers/caregivers/relatives of five (5) mentally ill persons. Library and internet desk research in its related literature were also employed. General findings of the study showed that caring for a mentally ill is burdensome. Data analysis revealed four superordinate themes under the experiences of caregivers, these consists of 1) caregiving difficulties, 2) various emotional reactions, 3) attitude towards the situation, and 4) positive caregiving experiences. Several support programs and services such as provision of mental health education and counseling regarding facts about the illness, its treatment and management, and leniency on watcher requirements during hospital admission are recommended to facilitate better caregiving experience of carers of the mentally ill.
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Dam, Kristianna, and Elisabeth OC Hall. "Childhood experiences pursue adulthood for better and worse: a qualitative study of adults' experiences after growing up with a severely mentally ill parent in a small-scale society." Journal of Research in Nursing 25, no. 6-7 (September 2020): 579–91. http://dx.doi.org/10.1177/1744987120942272.

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Background Growing up with a severely mentally ill parent can impact on subsequent adult life, and it can be extra challenging in a society with a small population, known as a small-scale society. Life in a small-scale society is characterised by multiple close relationships, lack of anonymity and a conservative attitude towards normal behaviour. Aims To look at the impact of growing up with a mentally ill parent on adult life in a small-scale society. Methods Data from semistructured interviews with 11 adult children of severely mentally ill parents were reanalysed and subjected to secondary analysis. Results The additional analysis resulted in four central themes: ‘becoming open and courageous’, ‘seeking and giving help’, ‘feeling uncertain and different’ and ‘being resilient and sensitive’. These were conflated into an overarching theme: ‘childhood experiences track into adulthood for better and worse’. The themes elucidate a diverse big picture and encompass positive and challenging features of adult life in a small-scale society. Conclusions The study ends with recommendations for the early establishment of collaboration and family-focused interventions with mentally ill parents and their children.
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Balajadia, Kathleen Jose G., Christine C. Carlos, Dawnald Russel L. De la Cruz, and Angel Grace F. Bingcang. "Nursing Students’ Stigma on Mental Hospital Exposure: A Phenomenological Study." Abstract Proceedings International Scholars Conference 6, no. 1 (October 29, 2018): 115. http://dx.doi.org/10.35974/isc.v6i1.1421.

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Exposure to mentally ill clients is challenging because of the fear attached to it. Oftentimes, the mentally ill are viewed as dangerous, unpredictable, and bizarre, which brings fear to other individuals, including health professionals. Professional care providers suffer from common fears and apprehension upon contact with the patient. Professional stigma, which refers to the nursing students’ fears towards exposure to mentally ill patients, was explored in this study. The study utilized a phenomenological research design. Semi-structured interviews were conducted among ten nursing students from a university in Cavite and triangulation of the data using interviews with clinical instructors and blockmates was employed. Thematic analysis was done using Colaizzi’s approach. Findings showed that mental illness was considered as a poor coping mechanism that results in mental dysfunction, disturbance of a normal pattern of thinking, and a point of struggle to adjust to the society for acceptance. Themes that emerged regarding fear before mental health exposure were fear of physical harm or violence, transference, and inadequacy in delivery of care. However, after exposure, the fears were observed to be minimal. Based on the findings of the study, it was recommended that schools of nursing which expose their students in the psychiatric ward must include briefing and debriefing of students. Clinical instructors should orient nursing students prior to exposure to the mental ward to desensitize them. In addition, emphasis on the importance of increasing awareness on how stigma affects society and the mentally ill must be given importance in order to provide efficient nursing care.
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Sibiya, Maureen Nokuthula, Vasanthrie Naidoo, and Avela Mjajubana. "Experiences of Family Members of Persons With Mental Illness: A Qualitative Inquiry." Global Journal of Health Science 11, no. 9 (July 10, 2019): 78. http://dx.doi.org/10.5539/gjhs.v11n9p78.

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The shortage of skilled and experienced health workers, lack of facilities, limited psychiatric care and inaccessible mental health care services in the uMsunduzi Municipality in Northern KwaZulu-Natal are causes of concern. With limited access to health services and resources, family members have no choice, but to take care of mentally ill relatives. These underlying problems have warranted the need to explore the experiences of family members living with mentally ill relatives. A qualitative, exploratory, descriptive design was used to collect data by in-depth one-on-one interviews and findings were analyzed using Tesch’s method of data analysis. This study showed that the uMsunduzi Municipality needed assistance with resources to support family members living with their mentally ill relatives and family members’ lack of knowledge and experience emerged as a major factor that influenced the care, treatment and rehabilitation of their mentally ill relatives. Compounded by inadequate mental health facilities and infrastructure as well as  the implications of the non-implementation of the acts, policies, processes and procedures in the uMsunduzi Municipality; this study recommends the need to enhance community education of all health professionals, providing relevant training in mental illness management. A shared decision-making process is vital, so that a collaborative partnership between family members and health professionals across KZN is established. This will in turn enhance the lived experiences of family members and mentally ill patients.
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Chorna, V. V., V. M. Makhniuk, S. S. Khliestova, and N. I. Gumeniuk. "Assessment of the quality of medical services to relatives of the mentally ill who are in inpatient treatment." Biomedical and Biosocial Anthropology, no. 38 (September 30, 2020): 5–11. http://dx.doi.org/10.31393/bba38-2020-01.

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The mental state of the mentally ill is one of the most important factors in the treatment of the patient by a medical professional. But aggression, high-pitched communication, indifference of a doctor or health care worker can negatively affect the outcome of treatment and recovery of a patient with mental and behavioral disorders. The problem of modern medical deontology in Ukraine is the stigmatization of health workers to patients with mental disorders, which lead to self-stigmatization of both patients and their families. The purpose of the study is to enable the relatives of mentally ill people undergoing long-term inpatient treatment, to determine the quality of medical services in a psychoneurological hospital, to identify ethical and deontological shortcomings in the doctor’s relationship with relatives of mentally ill person, to determine the level of self-stigmatization in relatives of the patient by medical staff. The analysis of domestic and foreign scientific sources, bibliosemantic, analytical and statistical research methods were used in the work. A questionnaire was conducted (using a specially designed questionnaire) with elements of interviews of 92 respondents (relatives of mentally ill patients who were treated at a psychoneurological hospital in Vinnytsia). The results were processed using the licensed standardized package "Statistica 6.1". The need to comply with state building codes for health care facilities in accordance with European requirements has been proven. This will eliminate the feeling of hopelessness during hospitalization in public psychoneurological hospitals, which are a great trauma for relatives of patients. It has been shown that in order to prevent stigmatization of relatives of patients in psychoneurological hospitals, it is necessary to conduct trainings and interviews after training, which will determine the degree of stigmatization and subsequent preventive measures. It is shown that for relatives of mentally ill on the basis of psychoneurological hospitals it is necessary to equip rooms for psychodiagnostics and further psychocorrection. Development of affordable correctional programs for relatives of patients will reduce maladaptation and improve life satisfaction.
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Elmquist, L., M. Henriksen, and J. Nordgaard. "Why do mentally ill, homeless people use substances?" European Psychiatry 64, S1 (April 2021): S235. http://dx.doi.org/10.1192/j.eurpsy.2021.628.

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IntroductionIn the Danish social welfare system, few people are homeless solely for economic reasons. In fact, 38% of homeless people suffer from both substance use and a psychiatric disorder, making diagnostic assessment and treatment difficult. This patient group, with dual diagnoses, often fail to receive effective treatment, and the consequences are far reaching and detrimental. A more comprehensive grasp of the history and patterns of substance use in these patients may contribute to improve their treatment.ObjectivesTo identify the role and patterns of substance use in mentally ill, homeless people.Methods50 homeless, mentally ill patients are examined in comprehensive interviews, exploring the relationship between substance use, homelessness, and suffering from a mental disorder. The data are analyzed quantitatively as well as qualitatively using thematic analysis.ResultsPreliminary results indicate that substance use in mentally ill homeless patients is a complex phenomenon. On the one hand, substance use seems to contribute to keep the patient homeless and makes it difficult for the patient to get the necessary psychiatric help. On the other hand, substance use also appear to play an important part in coping with life on the streets by offering some kind of social contact and some relief from a desperate situation.ConclusionsIt seems that the triad of substance use, mental illness, and homelessness somehow reinforce each other and simultaneously locks the situation. New approaches for disentangling this locked situation and avoiding this ‘Bermuda triangle’ is needed.
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Dissertations / Theses on the topic "Mentally ill Victoria Interviews"

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Portillo, Carmen Julieta 1955. "RESOURCES AND OBSTACLES TO MENTAL HEALTH SERVICE UTILIZATION: INTERVIEWS WITH CHRONICALLY MENTALLY ILL MEXICAN AMERICAN CLIENTS AND SIGNIFICANT FAMILY MEMBERS." Thesis, The University of Arizona, 1986. http://hdl.handle.net/10150/291716.

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The intent of this study was to examine the perceived resources and obstacles which were related to the utilization of mental health services by chronically mentally ill Mexican American clients. Specifically, the study identified resources and obstacles encountered by six chronically mentally ill clients and six family members as they accessed various mental health services. The study was conducted in the fall of 1985 from clients currently receiving services from La Frontera Center, Inc., Tucson, Arizona. Data were interpreted through content analysis to conceptualize and categorize client and family member responses. Chronically mentally ill clients relied heavily on individuals such as friends, therapist and priest as resources for mental health service support. In contrast, family members focused primarily on institutions for resource support. Financial resources, institutional policies, denial, and the lack of personal direction were listed as obstacles to seeking mental health services by clients and family members. Study results suggested that the perceptions of traditional and nontraditional obstacles and resources by Mexican American clients and family members continue to strongly influence utilization of mental health services In particular, the issue of "stigma" and the personal qualities and abilities of the therapist emerged as significant descriptors in client and family member self statements.
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Brooks, Margaret J. P. "Beyond the divide: women's experiences in rural Victorian psychiatric rehabilitation services." Thesis, 2003. https://vuir.vu.edu.au/18145/.

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The objective of this study was to give voice to women experiencing psychiatric rehabilitation services in rural Victoria. A critical analysis of the literature revealed a landscape of marginalisation and alienation for women experiencing a mental illness in a rural area. This study used a phenomenological method to explore the meanings of women's experiences. The understanding of meaning was developed through a dual perspective with women experiencing rural psychiatric rehabilitation and workers who delivered these services. The research centred on the voices of the women but encouraged a personal and collective reflective approach with workers. As the researcher I also took a reflexive approach which highlighted the methodology as an evolving and ongoing process and demonstrated the integral nature of the researcher in the research process. A chapter on locating the researcher was included as part this reflective process. The analysis of the collective stories produced a rich diversity of material was drawn together thematically to include: • Reflections of struggle; • Long way from anywhere: • The rural dimension; • Construction of a caring relationship, and, • Interlinking care. Through this thesis I argue that women are marginalised and alienated by social cultural conditions of their lives which impacts on their mental illness and rural experiences. However, women are not a homogenous group and a diversity of experiences exists which demonstrates women's active capacity to mediate their environment. As active participants in their psychiatric rehabilitation care the women were able to shift their identity from one of powerlessness and lack of control towards regaining control and managing their illness and environment. The thesis is a story of transformation as the women progressively moved forward in their journey.
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Books on the topic "Mentally ill Victoria Interviews"

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Integrity, Victoria Office of Police. Policing people who appear to be mentally ill. [Melbourne, VIC]: Victorian Government Printer, 2012.

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Coleborne, Catharine. Reading 'madness': Gender and difference in the colonial asylum in Victoria, Australia, 1848-1880s. Perth, W. A: Network Books, 2007.

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Shavelson, Lonny. I'm not crazy, I just lost my glasses. Berkeley, CA: De Novo Press, 1986.

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H, Gudjonsson Gisli, and Great Britain. Royal Commission on Criminal Justice., eds. Persons at risk during interviews in police custody: The identification of vulnerabilities. London: HMSO, 1993.

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Feng zi de shi jie. Xianggang: Liang guang wen hua you xian gong si, 2010.

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Board, Victoria Mental Health Review. Decisions of the Mental Health Review Board, Victoria, 1987-1991. Melbourne: Mental Health Review Board, 1992.

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Law Reform Commission of Victoria. The concept of mental illness in the Mental Health Act 1986. Melbourne: The Commission, 1990.

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Tian cai zai zuo, feng zi zai you. Wuhan: Wuhan da xue chu ban she, 2010.

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Moser, Tilmann. Dabei war ich doch sein liebstes Kind: Eine Psychotherapie mit der Tochter eines SS-Mannes. München: Kösel, 1997.

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Garza, Cristina Rivera. La Castañeda: Narrativas dolientes desde el Manicomio General, México, 1910-1930. México, D.F: Tusquets, 2010.

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Book chapters on the topic "Mentally ill Victoria Interviews"

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Droegemueller, Bastian, Corinna Mielke, Reinhold Haux, and Alexander Diehl. "Acceptance Study on the Usage of Health-Enabling Technologies in Therapy and Diagnostics for People with Mental Disorders." In Studies in Health Technology and Informatics. IOS Press, 2020. http://dx.doi.org/10.3233/shti200694.

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Mental disorders are widespread among the world’s population and place a high burden on both the people affected and the economy. In this area of health care and prevention major deficits can be found. Health-enabling technologies are being developed in order to provide support in the therapy and diagnostics of mental disorders. However, it is not clear whether patients are open to these technologies and what they expect from a suitable usage. The main goal of this study is to find out what opinions, hopes and fears mentally ill persons have towards a supporting treatment with health-enabling technologies. Personal interviews were conducted with psychiatric patients for that purpose. The evaluation of the interview data revealed a predominantly positive mindset of the participants. In addition to the general question according to the acceptance, requirements and expectations for the use of health-enabling technologies were acquired. In this context the concern of an invasion of privacy was exposed as a major barrier.
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Söderström, Kerstin. "Bekymring for det ufødte liv og omsorgsovertakelse ved fødsel: Posisjoner, verdikonflikter og spenninger i tverrfaglig arbeid." In Verdier i barnevern, 131–51. Cappelen Damm Akademisk/NOASP, 2020. http://dx.doi.org/10.23865/noasp.103.ch7.

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Separating a mother and newborn at the maternity ward is a challenging, potentially traumatic, and value-laden intervention. Cross-disciplinary collaboration in this tense and intense situation ideally assists child protection services in reaching well-founded decisions. However, differing opinions, professional stances and values can jeopardize the decisional process and threaten the quality of care and rights of the client(s). The main aim is to describe and analyse cross-disciplinary teamwork during pregnancy and the process towards a child protection decision. Participant observation and interviews provided data and descriptions of the case study, analysed according to positioning theory. The results show how two main storylines, a medical-therapeutic and a child protection storyline, each with a set of professional positions, create friction and tension in cross-disciplinary collaboration. The case describes the initial tensions, how they were overcome, and how they finally resulted in a planned removal at birth. This gave the mentally ill mother-to-be the opportunity to participate and prepare for the separation. The study demonstrates how a supervised, structured and reflective collaborative process enabled the participants to deal with conflicts and uncertainties stemming from positions and the dynamics of positioning. Further research and practical experiences, e.g. through simulation training, are needed to inform safe and caring removal practices and validate the usefulness of positioning theory to illuminate interprofessional conflict.
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