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<p>The purpose of this study is to explore intersectionality of Religion/Spirituality and immigration in the experience of Romanian evangelicals in Canada from a Critical Realist perspective. In the first two chapters I provide background information outlining the interconnection between spirituality/religion, social work and immigration and examine the existing body of knowledge of present literature on ways of utilizing relevant concepts, methods, emerging themes and I address some of the implications and critiques pertaining to the literature perused. In the following two chapters I present the theoretical framework of Critical Realism, the methodological approach utilized -Interpretative Phenomenological Analysis, and the dual gathering methods employed, semi-structured interviews and poetic inquiry. In the main part of the theses I review the findings and discuss them from a theoretical and practical perspective, concluding with a number of recommendations and observations which, if implemented, would in my opinion effect a more spiritually sensitive practice in working with specific ethno-religious groups.</p> / Master of Social Work (MSW)

From being a fictional element in sci-fi, voice control has become a reality, with inventions such as Apple's Siri, and interactive voice response (IVR) when calling your doctor's office. The combination of radio’s strength as a hands-free medium, public radio’s mission to reach across all platforms and the rise of voice makes up a relevant intersection; voice controlled public radio in Sweden. This thesis has aimed to investigate how radio listeners wish to interact using voice control to listen to on-demand radio content. Additionally, what does public radio need to consider when implementing the UX for voice control? A questionnaire, Google Analytics-data from Sveriges Radio’s mobile app and website, and an interview with National Public Radio were used to determine four initial functions voice controlled on-demand. The functions were turned into four scenarios, used as the basis for a workshop and brainstorming session. Three of these scenarios were then selected to be the foundation for a Wizard of Oz-prototype, which six users evaluated. The results indicate that to create a viable voice user interface (VUI) for radio, there needs to be a profile for the user to create a personalized experience, with filtered searches created by user behaviour and preference settings. The VUI also needs to allow synonyms for program names, as well as keyword tag material for clustering similar material and to enable personalized user searches. This keyword-system can further be utilized to give user recommendations based on behaviour and preferences. A companion application with a graphical user interface (GUI) can be used for such functionality as settings, help, queuing and creating playlists. Finally, the system needs to ensure that the users are taken care of and guided. A radio host can be used as a basis for the system's persona, to create a consistent and familiar interface. Aspects to examine in the future are more extensive user testing for the VUI design, filter bubbles, ensuring that the user data is not misused or leaked, dimensions of the system's persona, the future of radio and the progress of IPAs.

Yes / In this article we address how relatives of people with frontal-variant frontotemporal dementia (fvFTD) experience the illness and how it impacts their lives. We interviewed 6 participants and carried out interpretative phenomenological analysis. We report on 11 themes that reflect distinctive challenges. Five themes relate to witnessing bizarre and strange changes: changed appetites and drives, loss of planning ability, loss of inhibition leading to social embarrassment, risky behavior, and communication problems. Four relate to managing these changes and two to the impact on the person and his or her relationships. Relatives must live with unusual changes in the person with fvFTD and the stigma this carries in social settings. They learn to act assertively for their relatives and put effort into promoting quality of life, using strategies adapted for fvFTD. Relatives grieve the loss of the person with fvFTD and their mutual relationship, but nonetheless find sources of solace and hope.

人體乃傳播最原初的源頭，人們會依據當代社會的主流身體規範規訓自己的身體，傳遞背後所代表的價值，也依此形塑自我認同。當前社會認定標準女體的要件中，我們往往都忽略了「沒有體毛」也是一項相當重要的條件。對女人來說，體毛的去留具有相當的政治性，並佔據做女人（being woman）過程的重要戰略位置。本研究探討女性在規訓身體時，其如何理解社會規範，並聚焦女性雷射除毛的動機、目的及經驗，又她們賦予它什麼意義。另外，也探詢女性身份認同與理解策略之間的關係。 / Human body is the most primal mean of communication, people discipline their body according to body norms of modern society. Body is used to be a message carrier, we change our appearances to express the valufe that we believe and shape our identification also. While we are familiar with the traits that constitute the "ideal female body" as defined by modern society, we often overlook the fact that "absence of body hair" is also an important trait as such. The women's decision of whether to keep or remove body hair has always had political implications. It is of strategic importance in the process of "being female". This thesis focus on motive、 intention and experience of laser hair removal of Taiwan’s working girls. Explore how does the subject make sense about the norm of hair removal and the relationship between feminine identification and strategy of comprehension.

Aim: According to the existing evidence-base, the experience of the death of a therapy client (from a cause other than suicide) for Clinical Psychologists is substantially under researched. Moreover, previous studies into the experience of patient or client death for healthcare professionals indicate this may be an important focus for research. The present study aimed to explore the often unheard, lived experiences of client death for Clinical Psychologists at the beginning of their career. It was hoped that these research findings may assist training courses, clinical supervisors and other Psychologists of all grades to make sense of this experience in greater depth. Method: A qualitative approach was adopted for this study. Semi-structured interviews were conducted with nine female junior Clinical Psychologists (Trainee, Newly Qualified) who had experienced the death of a client. The accounts were analysed using IPA, which attempts to illuminate the lived experience of a phenomenon for small samples of individuals. Results: The analytic procedure highlighted three main themes as emerging from participants’ accounts in the context of their client’s death: Connected and affected: Being unprepared for initial reactions to the client's death; "we do it so why can't you?" facing institutional denial and avoidance; "It's not something I've forgotten about", The lasting impact of client death: Learning reluctant lessons and experiencing continuing bonds. Implications: This study highlights the importance of recognising the impact of client death on Clinical Psychologists in particular, and healthcare professionals in general. Client death, by all causes, appears much overlooked within the current research base, which may have led to a self-perpetuating cycle of hidden and unspoken stories. The findings indicate death needs to be on the research and teaching agenda within the institution of Clinical Psychology. As a result we may be able to begin to break the current cycle of silence which has served to potentially disservice us as professionals, our teams and most importantly our clients.

Perfectionism can be constructed as a trans diagnostic concept that co exists and probably contributes to the onset development and maintenance of a number of Axis 1 disorders. There is also a significant relationship between perfectionism and low self- esteem. There is considerable theoretical debate in the literature concerning whether perfectionism is uni or multi-dimensional with most therapies being based upon uni dimensional conceptualisations and thus overlooking interpersonal factors. This is also reflected in the relative absence of qualitative studies that explore perfectionism from a lived experience perspective. Aims: This study aims to explore the experiences of perfectionism and low self-esteem in different life domains. It also aims to evaluate the client’s experiences and efficacy of a proposed treatment protocol that targets perfectionism from a multidimensional perspective. Method: The study is divided into three phases. A Multiple baseline design is used to evaluate the treatment protocol including cognitive and behavioural interventions, compassionate mind training and assertiveness training to target perfectionism and low self-esteem. Two clinical groups experiencing Axis 1 disorders and high perfectionism are divided amongst the different phases of this study, 13 and 8 participants respectively. Mixed methods are administered to analyse the data with greater emphasis on the qualitative ones. Measures administered include the Beck Depression & Anxiety Inventories; the Rosenberg Self Esteem Scale; the Dysfunctional Attitudes Scale; the Multidimensional Perfectionism Scale by Frost and the Perfectionistic Self Presentation Scale. 8 semi-structured interviews are analysed utilising Interpretative Phenomenological Approach (IPA). Results: from the analysis of data it is evident that perfectionism is a multidimensional construct with strong interpersonal features that affect several different life domains. The proposed treatment protocol appears significantly effective in reducing perfectionism and Axis 1 disorder symptomatology. Additionally, there is a significant increase in self- esteem. Interventions that appear most helpful are behavioural experiments, assertiveness training, compassionate mind training, continuum and positive logging.

Mémoire numérisé par la Direction des bibliothèques de l'Université de Montréal.

<p>Syftet med studien var att med kvalitativ metod försöka förstå hur individer medAspergers syndrom förhåller sig till sin diagnos och sin funktionsnedsättning i sinblogg. I en ambition att nå ett inifrånperspektiv kom bloggtexter att analyserasenligt en tolkande fenomenologisk ansats (IPA). Stor vikt har lagts vid att förhållasig till etiska riktlinjer för Internetforskning och att behålla bloggskribenternaskonfidentialitet. Det senare medförde till exempel att citat från bloggtexterna inteförekommer i arbetet. I bloggtexterna har dels tre mer genomgående temanutkristalliserats. Dessa är diagnosen Aspergers syndrom, kompenserandet förfunktionsnedsättningen och bloggandet i sig. Dels har tre mer komplexa ochövergripande teman identifierats som dessutom kan utgöra tre olika blickar tillvilka bloggskribenterna förhåller sig. Samhällets blick ger individen möjlighet attkomma ut som Asperger, kollektivets blick ger individen möjlighet att reclaimaAspergern och individens blick hanterar individens konst att vara normal.</p>

Syftet med studien var att med kvalitativ metod försöka förstå hur individer medAspergers syndrom förhåller sig till sin diagnos och sin funktionsnedsättning i sinblogg. I en ambition att nå ett inifrånperspektiv kom bloggtexter att analyserasenligt en tolkande fenomenologisk ansats (IPA). Stor vikt har lagts vid att förhållasig till etiska riktlinjer för Internetforskning och att behålla bloggskribenternaskonfidentialitet. Det senare medförde till exempel att citat från bloggtexterna inteförekommer i arbetet. I bloggtexterna har dels tre mer genomgående temanutkristalliserats. Dessa är diagnosen Aspergers syndrom, kompenserandet förfunktionsnedsättningen och bloggandet i sig. Dels har tre mer komplexa ochövergripande teman identifierats som dessutom kan utgöra tre olika blickar tillvilka bloggskribenterna förhåller sig. Samhällets blick ger individen möjlighet attkomma ut som Asperger, kollektivets blick ger individen möjlighet att reclaimaAspergern och individens blick hanterar individens konst att vara normal.