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Дисертації з теми "Life Style Disorders"

Автор: Grafiati

Опубліковано: 3 червня 2025

Оновлено: 31 липня 2025

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1

Boza, Juliana Catucci. "Qualidade de vida em pacientes adultos e pediátricos com vitiligo : estudo baseado em questionários de qualidade de vida genéricos e específicos." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2016. http://hdl.handle.net/10183/143643.

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Introdução: O vitiligo é uma doença da pele frequente que afeta cerca de 1% da população em todo o mundo. Ocorre em pessoas de qualquer idade ou etnia, e mais da metade dos pacientes desenvolvem a doença antes dos 20 anos de idade. O vitiligo pode afetar negativamente a qualidade de vida (QoL) do paciente. Um questionário de qualidade de vida específico para vitiligo foi desenvolvido e validado na língua inglesa: the vitiligo-specific quality-of-life instrument (VitiQoL). Objetivo: O objetivo deste estudo é avaliar a QoL em pacientes adultos com o VitiQoL e o DLQI e pediátricos com o CDLQI em

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2

Henje, Blom Eva. "Anxiety and depression in adolescent females autonomic regulation and differentiation /." Stockholm, 2010. http://diss.kib.ki.se/2010/978-91-7409-807-5/.

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3

Cox, Molly Havnen. "The similarity of mothers' and daughters' coping style, and its relationship to disordered eating." Akron, OH : University of Akron, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=akron1194453199.

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Dissertation (Ph. D.)--University of Akron, Dept. of Counselor Education and Supervision, 2007.<br>"December, 2007." Title from electronic dissertation title page (viewed 02/27/2008) Advisor, Robert C. Schwartz; Committee members, Karyn Bobkoff Katz, Cynthia A. Reynolds, Sandra Spickard-Prettyman, Fred H. Ziegler; Department Chair, Karin B. Jordan; Dean of the College, Cynthia F. Capers; Dean of the Graduate School, George R. Newkome. Includes bibliographical references.

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4

Ngandu, Tiia. "Lifestyle-related risk factors in dementia and mild cognitive impairment : a population-based study /." Stockholm : Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, 2006. http://diss.kib.ki.se/2006/91-7140-744-8/.

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5

Holmberg, Sara. "Musculoskeletal disorders among farmers and referents, with special reference to occurrence, health care utilization and etiological factors : a population-based study /." Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4626.

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6

Sundelöf, Martin. "Aspects on prognosis of cancers of the oesophagus and gastric cardia /." Stockholm, 2006. http://diss.kib.ki.se/2006/91-7357-011-7/.

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7

Hajduk, Alexandra M. "Cognitive Status and Initiation of Lifestyle Changes Following Acute Coronary Heart Syndrome: A Dissertation." eScholarship@UMMS, 2014. https://escholarship.umassmed.edu/gsbs_diss/701.

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Background: Cognitive impairment is prevalent in survivors of acute coronary syndrome (ACS) and increases risk for poor outcomes. Lifestyle changes are recommended to patients after ACS to reduce their risk for recurrent events, but cognitively impaired patients may encounter difficulties initiating these changes. This dissertation had three aims: (1) to examine cognitive status as a predictor of lifestyle changes after ACS, (2) to examine whether caregiver support moderates the association of cognitive status and initiation of lifestyle changes, and (3) to assess the reliability of self-repor

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8

Hajduk, Alexandra M. "Cognitive Status and Initiation of Lifestyle Changes Following Acute Coronary Heart Syndrome: A Dissertation." eScholarship@UMMS, 2003. http://escholarship.umassmed.edu/gsbs_diss/701.

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Background: Cognitive impairment is prevalent in survivors of acute coronary syndrome (ACS) and increases risk for poor outcomes. Lifestyle changes are recommended to patients after ACS to reduce their risk for recurrent events, but cognitively impaired patients may encounter difficulties initiating these changes. This dissertation had three aims: (1) to examine cognitive status as a predictor of lifestyle changes after ACS, (2) to examine whether caregiver support moderates the association of cognitive status and initiation of lifestyle changes, and (3) to assess the reliability of self-repor

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9

Novak, Masuma. "Social inequity in health explanation from a life course and gender perspective /." Doctoral thesis, Umeå : Umeå university, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-31849.

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10

Carniel, Joana Desirée. "Ciclo vigília/sono e a saúde dos adolescentes." Universidade do Estado de Santa Catarina, 2014. http://tede.udesc.br/handle/handle/286.

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Made available in DSpace on 2016-12-06T17:07:01Z (GMT). No. of bitstreams: 1 Joana Carniel - Dissertacao.pdf: 1480883 bytes, checksum: 0e7aa3c6da93e8b4a83835b3d8e72d16 (MD5) Previous issue date: 2014-06-25<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>During the teenage years, there are significant alterations in the expression of the Sleep-Wake Cycle with great consequences for health. The two main objectives of this study were to validate the Pediatric Daytime Sleepiness Scale (PDSS) for the Brazilian Portuguese and analyze the associations between the matters of health

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11

Greenberg, Sarah. "Attachment Style, Perceived Life Events, and Psychological Well-Being in Adults Coping with Bipolar Disorder: A Longitudinal Study." Bowling Green State University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1402670377.

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12

Knappe, Susanne, Roselind Lieb, Katja Beesdo, et al. "The Role of Parental Psychopathology and Family Environment for Social Anxiety Disorder in the First Three Decades of Life: parental psychopathology and family environment in social anxiety disorder." Technische Universität Dresden, 2009. https://tud.qucosa.de/id/qucosa%3A27047.

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Background. To examine the role of parental psychopathology and family environment for the risk of social anxiety disorder (SAD) in offspring from childhood to early adulthood, covering an observational period of 10 years. Method. A community sample of 1,395 adolescents (aged 14 to 17 years at baseline) was prospectively followed-up over the core high risk period for SAD onset. DSM-IV offspring and parental psychopathology was assessed using the Munich-Composite International Diagnostic Interview; direct diagnostic interviews in parents were supplemented by family history reports from offspri

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13

Knappe, Susanne, Roselind Lieb, Katja Beesdo, et al. "The Role of Parental Psychopathology and Family Environment for Social Anxiety Disorder in the First Three Decades of Life." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2013. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-118265.

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Background. To examine the role of parental psychopathology and family environment for the risk of social anxiety disorder (SAD) in offspring from childhood to early adulthood, covering an observational period of 10 years. Method. A community sample of 1,395 adolescents (aged 14 to 17 years at baseline) was prospectively followed-up over the core high risk period for SAD onset. DSM-IV offspring and parental psychopathology was assessed using the Munich-Composite International Diagnostic Interview; direct diagnostic interviews in parents were supplemented by family history reports from offspri

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14

Webster, Tabitha Nicole. "Shame Not the Same for Different Styles of Blame: Shame as a Mediating Variable for Severity of Childhood Sexual Abuse and Trauma Symptoms in Three Attribution of Blame Groups." BYU ScholarsArchive, 2013. https://scholarsarchive.byu.edu/etd/4046.

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This study examined the role of internalized shame in mediating the relationship between severity of childhood sexual abuse and adult symptoms in three groups based on attribution of blame. The random community sample of 318 female survivors completed the Trauma Symptom Checklist-40 (Briere, 1996), Internalized Shame Scale (Cook, 2001), questions about frequency of abuse, duration, and specific characteristics (no physical contact to vaginal/anal intercourse with force) and the degree to which they blamed self, fate, or perpetrator. It was hypothesized that severity (measured by abuse characte

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15

Raymond, Kathryn Y. "Parents Caring for Adult Children With Serious Mental Illness: A Qualitative Descriptive Study: A Dissertation." eScholarship@UMMS, 2016. https://escholarship.umassmed.edu/gsn_diss/40.

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The purpose of this study was to examine parents’ management styles when caring for adult children with serious mental illness (SMI), as well as parents’ perspectives on what type of community-based mental health interventions would support and/or enhance overall family functioning. This qualitative descriptive study was undergirded by Knafl and Deatrick’s Family Management Style Framework. Thirty parents (N = 30) caring for adult children with SMI over age 18 were recruited as participants. Demographic data included age, gender, ethnicity, educational level, annual income, and National Allian

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16

Swanston, Heather Yvette. "Five Years After Child Sexual Abuse." University of Sydney. Paediatrics and Child Health, 2000. http://hdl.handle.net/2123/573.

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Introduction Child sexual abuse is a common problem. Psychological and behavioural problems in children and adults who have experienced child sexual abuse have been associated with the abuse. Little research has been conducted which has been long-term, prospective, involved substantiated sexual abuse, included a control group, took into account mediating factors, utilised multiple data sources, relied on standardised measures and had a high follow-up rate. Aim The aims of this study were to compare a cohort of sexually abused young people with a group of nonabused peers and to establish

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17

Swanston, Heather Yvette. "Five Years After Child Sexual Abuse." Thesis, The University of Sydney, 1999. http://hdl.handle.net/2123/573.

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Introduction Child sexual abuse is a common problem. Psychological and behavioural problems in children and adults who have experienced child sexual abuse have been associated with the abuse. Little research has been conducted which has been long-term, prospective, involved substantiated sexual abuse, included a control group, took into account mediating factors, utilised multiple data sources, relied on standardised measures and had a high follow-up rate. Aim The aims of this study were to compare a cohort of sexually abused young people with a group of nonabused peers and to establish

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18

Lin, Mei-Chen, and 林玫珍. "The influence of caring burden, health locus of control and coping style of the chronic mental disorder’s primary caregivers on their quality of life." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/31336740601540351247.

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碩士<br>中原大學<br>心理學研究所<br>101<br>Abstract The care burden of the chronic mental disorders is now passed from the medical profession unto the patient’s family as the psychiatric treatment models put emphasis on deinstitutionalization and community rehabilitation，and on that account, the family caregivers feel much more burdensome. The past researches focused more on the relationship of the caregiver’s care burden and the life quality than on the caregiver’s adaptation process. Therefore, the purpose of this study is: to understand the effect on the caregiver’s life quality by their health locus o

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