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As social beings, we experience ourselves through interactions with others in daily routines that participate in the cultural practices and power relations of broader social structures. Social workers, and social scientists in general, however, have had difficulty conceptualizing and synthesizing this way of being in the world. This paper attempts to respond to that gap by discussing how clinical social workers can use the concept of working models as a tool for listening and understanding in psychotherapy. Utilizing a case example, the paper will discuss three working models, the enactment of power relations, cultural practices, and psychological processes, which provide an integrative framework to inform clinical work.
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This article reports data collected from a national survey of the Association for Gerontology in Higher Education’s (AGHE) member institutions conducted in 1998. The purpose was to explore current usage of distance learning in gerontological education. The findings suggest that distance learning is being implemented within various programs throughout the country with many others showing an interest. The strengths and limitations of using distance learning in gerontological education are discussed. [Article copies available for a fee from The Haworth Document Delivery Service: 1-800-342-9678. E-mail address: <getinfo@haworthpressinc.com> Website: <http://www.HaworthPress.com>]. © 2001 by The Haworth Press, Inc. All rights reserved.
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SUMMARY: Practice with working-class gay and bisexual men draws upon an ecological framework with a strengths perspective, which emphasizes the roles of culture, values, social class, social identity development, social categorization, social comparison, oppression and power, diversity, and stigma. This practice is based upon a process of developing an assessment and selecting a range of human service interventions. Ethnographic studies were conducted throughout the United States and Canada using a broad-based sample of working-class men to enhance our understanding of their needs and effective ways of helping. © 2001, Taylor & Francis Group, LLC.
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This report describes the qualitative component of a large-scale study of supported socialization. Paralleling the recent advances made through supported housing, supported employment, and supported education, this approach seeks to increase the involvement of individuals with psychiatric disabilities in naturally occurring social and recreational activities in community settings of their choice. After a review of social relationships and psychiatric disability, we describe the Partnership Project and present findings from a series of qualitative interviews conducted with a subsample of participants. We then discuss the implications of these findings for the community integration of individuals with psychiatric disabilities.
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“The Role of Readability in Today's Classrooms” emphasizes the importance of providing students with materials on the appropriate level of challenge. Major readability formulas and leveling systems that might be used to assess the difficulty level of materials are reviewed. Because formulas are restricted to objective factors and leveling systems rely too heavily on subjective judgment, this article recommends using both objective and subjective factors when estimating readability levels. This article also recommends using readability/leveling systems as a way of noting textual difficulties that might need instructional intervention.
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Women are often faced with the primary role of providing care for individuals with Alzheimer's disease (AD). This study explored women caregiver's perceptions of caregiving through the use of Cognitive Mapping (CM), a qualitative research method. Volunteers were recruited from caregiver support groups to construct maps of their experience of "caregiving for someone with AD." Maps were analyzed for commonly identified concepts and relationships. Twelve participants identified 280 concepts, 206 of which were unduplicated. Concepts were collapsed into 17 categories; the largest concepts being "friends and family," "sad," "frustration," and "time." The maps produced by the sample in this study were unique, providing evidence that the experience of AD caregiving varies significantly among caregivers. CM appears to be effective for identifying caregiver stressors and needed support services.
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Surveys estimate that 3-6% of the patients seen by physicians are gay or lesbian. There are unique health risks of gays and lesbians that are important to the clinician in determining an accurate diagnosis, providing patient education, and arriving at an appropriate treatment plan. One of the most significant medical risks of these populations includes avoidance of routine health care and dissatisfaction with healthcare. Many of these healthcare risks are not addressed because of lack of communication based on a number of common assumptions including the assumption that the patient is heterosexual. This article includes a summary of the medical literature through computerized searches to March 2002 in MEDLINE, PsychInfo, HEALTHSTAR, and bibliographies in articles on health care with gay and lesbian patients. The search strategy included health care of gays and lesbians and clinician-patient communication, partner and family issues. Secondly, it will examine common communication barriers and provide strategies for enhancing communication with patients in a gender-neutral, non-judgmental manner including suggestions for enlisting the inclusion of patients' families. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
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