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Autor/inHall, Sarah A.
TitelThe Social Inclusion of Young Adults with Intellectual Disabilities: A Phenomenology of Their Experiences
Quelle(2010), (133 Seiten)
PDF als Volltext Verfügbarkeit 
Ph.D. Dissertation, The University of Nebraska - Lincoln
Spracheenglisch
Dokumenttypgedruckt; online; Monographie
ISBN978-1-1096-8662-3
SchlagwörterHochschulschrift; Dissertation; Research Design; Qualitative Research; Mental Retardation; Quality of Life; Social Integration; Inclusion; Young Adults; Phenomenology; Bias; Interpersonal Relationship; Interviews; Volunteers; Work Environment; Leisure Time; Social Life; Self Determination; Housing; Transportation; Income; Financial Support; Family Relationship
AbstractSocial inclusion enhances the quality of life of young adults with intellectual disabilities (ID). Young adults with ID continue to face prejudice and discrimination that limit their social inclusion. They experience limited social inclusion because there are not enough appropriate activities available and they have limited opportunities to develop friendships. The social inclusion that people with disabilities experience within their local community varies greatly. There is a deficiency in the literature concerning the social inclusion of young adults with ID. Previous considerations of disability have focused primarily on physical access and reflect the local contexts in which the participants live. There is a need to understand the social inclusion of young adults with ID and to advocate for change. The purpose of the present study was to describe the social inclusion of young adults with intellectual disabilities and to identify contexts that limit or enhance their social inclusion. Social inclusion was defined as being involved in activities, developing and maintaining relationships, and having a sense of belonging. Participants included fourteen adults from 22 to 35 years of age with a mild or moderate intellectual disability who were able to verbally communicate their thoughts and experiences. I used the phenomenological qualitative research design to explore the lived experiences of social inclusion for young adults with ID. I collected data through semi-structured interviews. During the interviews, I asked the participants open-ended questions about their experiences of social inclusion and the context of their experiences. The length of each interview session and number of sessions were flexible to accommodate the needs of the participants. The findings consisted of themes that described their experiences of social inclusion and the contexts of their experiences. Their social inclusion consisted of involvement in work, volunteer, social, recreational, and leisure activities; reciprocal relationships; and the sense of belonging derived from accepting environments and self-determination. Their social inclusion was influenced by the contexts of their experiences including living accommodations, transportation options, personal abilities and skills, financial resources, assistance from family members, and assistance from service providers. [The dissertation citations contained here are published with the permission of ProQuest LLC. Further reproduction is prohibited without permission. Copies of dissertations may be obtained by Telephone (800) 1-800-521-0600. Web page: http://www.proquest.com/en-US/products/dissertations/individuals.shtml.] (As Provided).
AnmerkungenProQuest LLC. 789 East Eisenhower Parkway, P.O. Box 1346, Ann Arbor, MI 48106. Tel: 800-521-0600; Web site: http://www.proquest.com/en-US/products/dissertations/individuals.shtml
Erfasst vonERIC (Education Resources Information Center), Washington, DC
Update2017/4/10
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