Dissertations / Theses on the topic 'Obsessive-Compulsive Disorders (OCD)'
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Duba, Sauerheber Jill, and James Robert Bitter. "Anxiety and Obsessive Compulsive Disorders." Digital Commons @ East Tennessee State University, 2014. https://dc.etsu.edu/etsu-works/5222.
Full textWatkins, Laura H. A. "Cognitive dysfunction in Huntington's disease and related disorders." Thesis, University of Cambridge, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.313852.
Full textHalldorsson, Brynjar. ""Please help me" : excessive reassurance seeking as an interpersonal process in obsessive compulsive disorder and health anxiety." Thesis, University of Bath, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.646143.
Full textLipton, M. "Phenomenology of intrusive imagery in obsessive compulsive disorder (OCD)." Thesis, University College London (University of London), 2008. http://discovery.ucl.ac.uk/1444223/.
Full textLi, Yiu-bun, and 李耀斌. "Comorbid obsessive-compulsive symptoms (OCSs) and obsessive-compulsive disorder (OCD) in patients with schizophrenia treated with clozapine or haloperidol." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/200383.
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Master of Psychological Medicine
Domènech, Salgado Laura 1989. "A Comprehensive multiomics approach towards understanding obsessive-compulsive disorder." Doctoral thesis, Universitat Pompeu Fabra, 2018. http://hdl.handle.net/10803/665800.
Full textFins a dia d’avui, s’ha avançat molt poc a l’hora d’elucidar les causes genètiques del trastorn obsessiu compulsiu (TOC). En aquest projecte hem realitzat estudis d’associació de variants rares (RVAS) i anàlisis de transcriptòmica i metagenòmica per centrar-nos en àrees relativament poc explorades del TOC. Hem identificat i replicat un enriquiment de variants rares a TMEM63A, un gen que codifica un canal catiònic permeable per calci, a través d’anàlisis de seqüenciació de l’exoma complet, RVAS i reseqüenciació dirigida. A més, hem observat una sobrerepresentació de gens enriquits en variants rares en casos de TOC relacionats amb la senyalització de calci. Els estudis de transcriptòmica han identificat una expressió diferencial de gens involucrats en el desenvolupament i la funció neuronal en els pacients de TOC. La integració dels resultats dels nostres estudis de RVAS i transcriptòmica també revelen un possible paper de les semaforines i del guiatge axonal al TOC. Finalment, els estudis de metagenòmica han confirmat el increment prèviament reportat de la família bacterial Rikenellaceae en el microbioma intestinal i han mostrat una relació significativa més alta d’Actinobacteris/Fusobacteris en el microbioma de l’orofaringe dels pacients de TOC. Els nostres resultats fomenten activament la recerca en aquestes àrees.
Bonadio, Christopher N. "Evolutionary Origins of Obsessive-Compulsive Disorder and Depression." Kent State University / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=kent1216030443.
Full textBailey, Fiona Jane, and mikewood@deakin edu au. "The origins of inflated responsibility in obsessive compulsive disorder." Deakin University. School of Psychology, 2002. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20050902.121410.
Full textBoutros, Jean-Charles. "La philosophie vive plutôt que la philosophie à vif : Socrate aux périls de Marsyas : recherches sur les modes d'influence chez Platon, précédées d'une étude générale sur la magie et la pensée magique." Thesis, Paris 1, 2013. http://www.theses.fr/2013PA010717/document.
Full textTo explain the modes of influence operating in Plato’s Dialogues, we study how Socrates and others use their magic as several interlocutors have called Socrates a sorcerer. A framework is given to our research with a preliminary general study about magic covering anthropology, rituals – pathological (obsessive-compulsive disorders) or cultural – and magical thought. In Plato’s works, the way people think is influenced by many factors often unknowingly: personality, habits, society, ethics, ignorance, etc. Since it had been analyzed by Gorgias, speech experts, such as orators or sophists, have been using oratorical magic in their performances. And then the ambiguity of Socrates’ magic blatantly appears whereas he claims to refute falsehood and eliminate illusions. Different types of possession occur in Phaedrus, some uncontrolled, other controlled, entailing an initiation. Socrates carries out his magic in several striking cases of bewitchment and he also uses incantations in particular to sooth the fear of death. In the political field, the lawgiver finds an interest in using incantations for more effectiveness in his task since they can shape the forms of behaviors, create strong bond between citizens and contribute to social control. A law about crimes of magic is also designed
Souza, Fernanda Pasquoto de. "Tradução, adaptação e validação das escalas Obsessive-Compulsive Inventory - OCI e do Obsessive-Compulsive Inventory-Revised - OCI-R." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2008. http://hdl.handle.net/10183/13422.
Full textThe aim of the present project was to translate and adapt the scales Obsessive- Compulsive Inventory (OCI) and Obsessive-Compulsive Inventory-Revised (OCI-R) to Brazilian Portuguese and to evaluate the psychometric properties of the OCI-R, which measures the severity of the obsessive-compulsive symptoms. The project was developed in two stages: (1) the translation, transcultural adaptation and back-translation of the scales and (2) the study of reliability and validity of the questionnaire OCI-R in a clinical population and in a non-clinical sample (controls). The advantages of those scales, compared to the existent ones, are: (a) they are selfreported and (b) they produce scores for specific categories of obsessive-compulsive symptoms. In the first stage, the OCI and OCI-R, developed by the Center for the Treatment and Study of Anxiety, University of Pennsylvania, EUA were translated and adapted to the Brazilian Portuguese language. The scales were initially translated into Brazilian Portuguese by two bilingual psychiatrists and then independently back-translated by other two bilingual psychiatrists. The scales were then applied to 15 Obsessive Compulsive Disorder (OCD) patients, deliberately chosen from different educational levels, to make language adjustments. The author accepted the final version of the OCI and OCI-R scales after their back translation. Scales showed to be easy to understand and fill in by individuals and may be used with OCD patients of different socioeconomic levels. The OCI e OCI-R scales, in their version adapted to Brazilian Portuguese, can help health professionals in screening potential OCD patients assess the severity of obsessive-compulsive symptoms and the reduction of them through different treatments. The translation and the adaptation will be reported in the paper nº. 1. The second stage of the project evaluated the psychometric properties of the Brazilian version of the OCI-R in a clinical and in a non- clinical (controls) samples. The reliability and validity of the Brazilian Portuguese version of the Obsessive–Compulsive Inventory – Revised (OCI-R) were examined in a clinical sample of 64 patients with Obsessive- Compulsive Disorder (OCD), 33 patients with Social Phobia and 33 patients with Panic Disorder plus a non-clinical sample of 130 employees of a general hospital. Results indicate that the OCI-R is a valid measure for identifying and assessing the severity of the six symptom subtypes of OCD. In each sample the overall and subscale scores demonstrated moderate to good internal consistency and good convergent and divergent validity. Furthermore, in patients with OCD, the inventory showed sensitivity to Cognitive-Behavioral Group Therapy (CBGT). Our findings indicate that the Brazilian Portuguese version of the OCI-R retains the psychometric properties of its original version. These results were also compared with the results of validation of the Spanish and German OCI-R versions. That phase will be reported in the paper nº. 2. The OCI-R Brazilian Portuguese version can help health professionals and patients to screen potential people with OCD. More than this, its use can identify clinical or sub clinical OCD patients. As it is a self-report scale, it facilitates the early awareness of the disease, which is relevant because patients may take several years to seek treatment for OCD. Moreover, the use of this instrument can help to develop educational programs which could ameliorate prevention, as well as focus efforts in intervention actions.
Kelly, Jeremy MacLaren. "Exploring Retrospective Biases In Obsessive Compulsive Disorder: An Experience-Sampling Study." OpenSIUC, 2017. https://opensiuc.lib.siu.edu/theses/2212.
Full textFruehauf, Lindsay Morgan. "Cognitive Control and Context Maintenance in Individuals with Obsessive-Compulsive Disorder (OCD)." BYU ScholarsArchive, 2019. https://scholarsarchive.byu.edu/etd/8476.
Full textNavarro, Trujillo Rodrigo. "Association of inflammation markers in young adult patients with Obsessive-compulsive disorder." Thesis, Uppsala universitet, Institutionen för medicinsk biokemi och mikrobiologi, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-355094.
Full textWatson, Hunna J. "Clinical and research developments in the treatment of paediatric obsessive-compulsive disorder." Curtin University of Technology, School of Psychology, Division of Health Sciences, 2007. http://espace.library.curtin.edu.au:80/R/?func=dbin-jump-full&object_id=115091.
Full textStudy 1 comprised the first known meta-analysis of randomised, controlled treatment trials (RCTs) for paediatric OCD. Included studies were limited to RCTs as they are the most scientifically valid means for determining treatment efficacy and provide a more accurate estimate of treatment effect by removing error variance associated with confounding variables. The literature search identified 13 RCTs containing 10 pharmacotherapy to control comparisons (N = 1016) and 5 CBT to control comparisons (N = 161). Random effects modelling yielded statistically significant pooled effect size (ES) estimates for pharmacotherapy (ES = 0.48, 95% CI = 0.36 to 0.61, p < .00001) and CBT (ES = 1.45, 95% CI = 0.68 to 2.22, p =.002). The results support the efficacy of CBT and pharmacotherapy, and confirm these approaches as the only two evidence-based treatments for paediatric OCD. Implications and suggestions for future research are discussed. The effectiveness of CBT provided impetus to further examine this treatment. Group CBT is an understudied treatment modality among children with OCD. It was hypothesised that group CBT would possess efficacy because of the effectiveness of individual CBT for children with OCD, the demonstrated effectiveness of group CBT among adults with OCD, the practical and therapeutic advantages afforded by a group treatment approach, and the embeddedness of the approach in robust psychological theory. The aim of the second study was to evaluate the efficacy of group CBT. The study comprised the largest known conducted randomised, placebo-controlled trial of group CBT for paediatric OCD.
Twenty-two children and adolescents with a primary diagnosis of OCD were randomly assigned to a 12-week program of group CBT or a credible psychological placebo. Children were assessed at baseline, end of treatment, and at 1 month follow-up. Outcome measures included the Children’s Yale-Brown Obsessive-Compulsive Scale, global measures of OCD severity, Children’s Depression Inventory, and parent- and child-rated measures of psychosocial functioning. An intention-to-treat analysis revealed that children in the group CBT condition had statistically significantly lower levels of symptomatology at posttreatment and follow-up compared to children in the placebo condition. Analysis of clinical significance showed that 91% of children that received CBT were ‘recovered’ or ‘improved’ at follow-up, whereas 73% of children in the placebo condition were ‘unchanged’. Effect size analysis using Cohen’s d derived an effect of 1.14 and 1.20 at posttreatment and follow-up, respectively. These effects are comparable to results from studies of individual CBT. This study supported group CBT as an effective treatment modality for paediatric OCD and demonstrated that the effect extends beyond placebo and nonspecific treatment factors. In addition to treatment efficacy, the inherent worth of a treatment lies in its adoption by the relevant clinical population. Children with OCD are known to be secretive and embarrassed about symptoms, and there is often a long delay between onset of symptoms and treatment-seeking (Simonds & Elliot, 2001). An important observation during the course of conducting the RCT was that a high rate (39%) of eligible families declined participation.
This led to the question, "What barriers prevent participation in group CBT for paediatric OCD?" Qualitative methodology was employed to address this research question. Eligible families that had declined participation in the RCT were contacted and invited to participate in semi-structured interviews that explored reasons for non-participation and positive and negative perceptions of group CBT. The average time between non-participation and interview was 1.33 years (SD = 3 months). Data were collected from nine families and thematic analysis methodology was utilised to identify emergent themes. Failure to participate was predicted by practical and attitudinal barriers. Practical barriers included a lack of time, distance, severity of OCD symptoms, financial, and child physical health. Attitudinal barriers included child embarrassment about OCD symptoms, child belief that therapy would be ineffective, fear of the social aspect of the group, lack of previous success with psychology, lack of trust in strangers, parental concern about the structure of the group, denial of a problem, and ‘not being ready for it’. Attitudinal barriers more frequently predicted treatment non-participation. Positive and negative perceptions of this treatment modality were informative. Parents showed no differences in preference for individual or group CBT. An important finding was that 56% of the children had not received treatment since parental expression of interest in the group CBT program. Application of the findings to methods that promote service utilisation is discussed.
Boulougouris, Vasileios. "Neuroanatomical & neurochemical modulation of cognitive flexibility : implications for obsessive-compulsive disorder (OCD)." Thesis, University of Cambridge, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611496.
Full textHemmings, S. M. J. "Investigating the molecular aetiology of Obsessive-compulsive disorder (OCD) and clinically-defined subsets of OCD." Thesis, Stellenbosch : Stellenbosch University, 2006. http://hdl.handle.net/10019.1/1256.
Full textENGLISH ABSTRACT: Obsessive-compulsive disorder (OCD), a debilitating psychiatric disorder, affects 2-3% of the general population, and represents a global health problem. Evidence from family studies suggests that genetic factors play a role in mediating disease development. However, the pattern of inheritance is not consistent with monogenic disorders, but is “genetically complex”. Case-control association analysis, which facilitates dissection of the genetic aetiology of complex disorders, has yielded many inconsistent results in OCD studies, making identification of predisposing alleles difficult. These discrepant findings can largely be attributed to inappropriate statistical methodology and the lack of OCD phenotypic resolution. Although classified as a single clinical entity according to structured algorithms, OCD probably represents a final common outcome of multiple underlying aetiologies. Thus, numerous clinical subtypes of the disorder have been proposed; these “intermediate” phenotypes may be more closely related to a particular genetic substrate than the higher order construct of OCD. Furthermore, although genes encoding serotonergic (5-HT) and dopaminergic components are most commonly investigated, it is likely that the behavioural manifestations of OCD are mediated by a broader network of interconnected neurotransmitter and signalling pathways. Consequently, the aim of the present study was two-fold: to address the factors that may have confounded previous genetic case-control association studies and to investigate the genetic aetiology of OCD phenotypes while accounting for these factors. Case and control individuals were drawn from the reportedly genetically homogeneous Afrikaner population. However, as no empirical evidence existed to support the absence of genetic substructure, which would confound genetic association studies, a Bayesian modelbased clustering algorithm (Structure), that groups individuals on the basis of observed genotype data, was employed to assess population stratification in both case and control Afrikaner subjects. OCD patients were clinically stratified by gender, symptom severity, age at onset, the presence of selected co-morbid disorders and the presence of selected symptom dimensions, to facilitate the identification of susceptibility genes more closely related with these subtypes. Candidate genes included those coding for components of the 5-HT (5-HT receptors 1Dβ, 2A, 2C and 6), dopaminergic (dopamine receptors 1, 2, 3 and 4, dopamine transporter and catechol-O-methyltransferase [COMT]), glutamatergic (glutamate receptor subunit 2B [GRIN2B]) and neurodevelopmental pathways (brain-derived neurotrophic factor [BDNF] and homeobox 8 [HoxB8]), as well as previously uninvestigated genes (angiotensinconverting enzyme I, inositol-trisphosphate, phospholipase-C-gamma 1 and estrogen receptor alpha). The relationship between variants in these genes and OCD (or OCD subtypes) was investigated in a single locus and a haplotype context, while meta-analyses using published population-based case-control association data were also conducted. Significant associations noted between distinct COMT variants and OCD implicated COMT in the development of a genetically discrete, gender-dependant, early-onset, tic-related phenotype in males. Furthermore, investigations of variations in BDNF and GRIN2B point towards a genetically distinct, neurodevelopmental subtype of the disorder, mediated, in males at least, primarily by dysfunctions in BDNF. The striking gender dimorphism noted in these associations indicates the possibility of an epigenetic hormonal influence. Moreover, the significant association of polymorphisms within GRIN2B, in both a single locus and haplotype context, suggests the involvement of this gene in mediating a phenotypic subtype characterised by an early-onset, more severe form of the disorder. The present investigation forms part of ongoing research to elucidate genetic components involved in the aetiopathology of OCD and OCD-related subtypes. Such studies may pave the way towards more efficacious pharmacotherapeutic strategies, which will ease the suffering of individuals who are afflicted with this incapacitating condition.
AFRIKAANSE OPSOMMING: Obsessiewe-kompulsiewe steuring (OKS) is 'n aftakelende psigiatriese siektetoestand wat 2- 3% van die algemene bevolking affekteer en 'n globale gesondheidsprobleem verteenwoordig. Familiestudies dui daarop dat genetiese faktore 'n rol in die ontwikkeling van hierdie siekte speel. Die patroon van oorerwing is egter nie verenigbaar met dié van monogeniese siektes nie, maar is geneties "kompleks". Geval-kontrole assosiasie-ontleding, wat die disseksie van die genetiese etiologie van komplekse siektes fasiliteer, het teenstrydige resultate in OKS gelewer en dit bemoeilik die identifikasie van predisponerende allele. Die teenstrydige bevindings kan grootliks aan ontoepaslike statistiese metodiek en die gebrek aan fenotipiese differensiasie in OKS toegeskryf word. Alhoewel dit volgens gestruktureer algoritmes as 'n enkele kliniese entiteit geklassifiseer word, verteenwoordig OKS waarskynlik die eindresultaat van veelvoudige onderliggende oorsake. Baie kliniese subtipes van die toestand is al voorgestel en dié "intermediêre' fenotipes mag nader verwant aan 'n spesifieke genetiese substraat as die hoër orde konsep van OKS wees. Verder, alhoewel die gene wat die serotonergiese (5-HT) en dopaminergiese komponente kodeer meestalondersoek word, is dit waarskynlik dat die gedragsmanifestasies van OKS deur 'n breër netwerk van intergekonnekteerde neuro-oordragstof- en seinoordragpaaie meegebring word Gevolglik was die doel van die huidige studie tweevoudig: om faktore wat vorige genetiese geval-kontrole assossiasie-studies verwar het aan te spreek en om die genetiese etiologie van OKS-fenotipes te ondersoek met in ag neming van hierdie faktore. Geval- en kontrole-individue is gekies uit die Afrikaner-bevolking wat as geneties homogeen beskryf kan word. Daar was geen empiriese bewyse vir die afwesigheid van 'n genetiese substruktuur (wat genetiese assossiasie-studies sou verwar),nie. Daarom is 'n Bayesiese model-gebaseerde groeperings-algoritme (Structure), wat individue op grond van waargenome genotipiese data groepeer, gebruik om die populasie-stratifikasie is beide gevalen kontrole- Afrikaner-individue te bepaal. OKS-pasiënte is klinies gestratifiseer volgens geslag, ernstigheid van simptome, ouderdom by aanvang van simptome, die teenwoordigheid van geselekteerde komorbiede siektetoestande en die teenwoordigheid van geselekteerde simptoomdimensies of -groepe, om die identifikasie van moontlike vatbaarheidsgene wat nader verwant is aan die verskillende subtipes te fasiliteer/vergemaklik. Kandidaatgene het ingesluit: dié wat kodeer vir komponente van die 5-HT-(5-HT reseptore IDB, 2A, 2C and 6), dopaminergiese (dopamienreseptore 1, 2, 3 and 4, dopamien-transporter and katesjol-O-metieltransferase [COMTJ), glutamatergiese (glutamaat-reseptor subeenheid 2B [GRIN2B]) and neuro-ontwikkelingspaaie (brein-gederiveerde neurotrofiese faktor [BDNF] en homeobox 8 [HoxB8]), sowel as die gene wat nie voorheen ondersoek is nie (angiotensien-omsettingsensiem I, inositol-trisfosfaat, fosfolipase-C-gamma 1 en estrogeen-reseptor alpha). Die verhouding tussen variante in hierdie gene en OKS (of OKS-subtipes) is ondersoek in 'n enkel-lokus en haplotipe konteks, en meta-analises, wat gepubliseerde bevolkings-gebaseerde geval-kontrole ontledingsdata gebruik het, is ook gedoen. Beduidende assosiasies gevind tussen spesifieke COMT-variante en OKS in mans, het daarop gedui dat COMT in die ontwikkeling van geneties-diskrete, vroeë-aanvang, senutrekking ("tics") -verwante fenotipe in mans betrokke is. Verder het ondersoeke van variasies in BDNF en GRIN2B daarop gedui dat 'n geneties-afsonderlike, neuro-ontwikkelings-subtipe van.OKS wat, ten minste in mans, primêr deur wanfunksie van BDNF meegebring word. Die opvallende geslags verskil wat in hierdie assosiasies gesien word, dui op die moontlikheid van 'n epigenetiese hormonale invloed. Bowendien, die beduidende assosiasie van polimorfismes in GRIN2B in beide die enkel-lokus en haplotipe konteks, dui op die betrokkenheid van hierdie geen in die meebring van 'n fenotipiese subtipe wat deur 'n vroeë aanvang, en meer ernstige vorm van die siekte gekenmerk word. Die huidige ondersoek vorm deel van voortgesette navorsmg om die genetiese komponente wat betrokke is by die etiopatologie van OKS en OKS-subtipes, bloot te lê. Sodanige studies kan die weg baan na meer doeltreffende farmakoterapeutiese strategieë wat die lyding van indi vidue wat deur hierdie aftakelende toestand geraak word, kan verlig.
Ozomaro, Uzoezi. "The Genetic and Functional Analysis of the Obsessive-Compulsive Disorder Spectrum." Scholarly Repository, 2011. http://scholarlyrepository.miami.edu/oa_dissertations/602.
Full textKeyes, Carly Victoria. "How young people make sense of developing and getting help for obsessive compulsive disorder." Thesis, University of Hertfordshire, 2016. http://hdl.handle.net/2299/17190.
Full textMayerovitch, Jamie Isaac. "Treatment seeking for obsessive-compulsive disorder : role of ocd symptons and comorbid psychiatric diagnoses." Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=30702.
Full textMayerovitch, Jamie Isaac. "Treatment seeking for obsessive-compulsive disorder, role of OCD symptoms and comorbid psychiatric diagnoses." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape4/PQDD_0034/MQ64406.pdf.
Full textMavrothalassitis, Mariaan Janet. "Trauma and the pathogenesis of OCD : a literature review." Thesis, Stellenbosch : Stellenbosch University, 2001. http://hdl.handle.net/10019.1/52593.
Full textENGLISH ABSTRACT: Post-traumatic stress disorder (PTSD) is the most recognised mental disorder stemming from severe psychological trauma. One of the differential diagnoses of post-traumatic stress disorder, amongst others, is obsessive-compulsive disorder (OGD). These two disorders overlap at some point in terms of symptomatology. More specifically, both are characterized by recurrent intrusive thoughts. It has been hypothesized that trauma may also be a significant source of OGD development. OGD and PTSD are disorders that present in adulthood, as well as in childhood and adolescence. It is shown that PTSD and OGD can present comorbidly in adulthood and it is theorized that it may also be the case in childhood and adolescence. Evidence of OGD developing in the context of trauma and theories of how this might have happened are presented. It is shown how complicated it is to distinguish between OGD developing in the wake of trauma and PTSD and the importance of such a distinction.
AFRIKAANSE OPSOMMING: Post-traumatiese Stresversteurig (PTSD) is een van die mees erkende sielkundigeversteurings wat ontwikkel na die blootstelling aan sielkundige trauma. Obsessiewe-kompulsieweversteuring (OGD) is, onder andere, een van die differensiële diagnoses van PTSD. Die twee versteurings oorvleuel ten opsigte van simptomalogie. Meer spesifiek word beide gekenmerk deur herhalende indringende gedagtes. Daar word tans gehipotiseer dat trauma nie net 'n rol in die ontwikkeling van PTSD speel nie maar ook 'n oorsaaklike rol het in die ontwikkeling van OGD. OGD en PTSD is versteurings wat kan voorkom tydens volwassenheid, asook tydens die kinderjare en adolessensie. Daar word bewys gedoen van PTSD en OGD wat saam voorkom gedurende volwassenheid en daar word geteoretiseer dat dit ook die geval mag wees tydens die kinderjare en adolessensie. Bewys word gelewer van OGD wat ontwikkel na blootstelling aan trauma en teorië ten opsigte van die ontwikkeling word aangebied. Die onderskeid tussen OGD wat na trauma blootstelling ontwikkel en PTSD is ingewikkeld, dog is die onderskeid baie belangrik in vele opsigte.
Chrisman, Alyssa. "“And We Weren’t Alone”: Portrayals of Obsessive-Compulsive Disorder in Young Adult Literature." The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1491942992382162.
Full textFarrell, Lara J., and n/a. "Obsessive-Compulsive Disorder Across the Developmental Trajectory: Clinical Correlates and Cognitive Processing of Threat." Griffith University. School of Applied Psychology, 2004. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20040513.132648.
Full textBudajeva, Snezjana. "OCD as behavioral addiction and the reward process : A systematic review." Thesis, Högskolan i Skövde, Institutionen för biovetenskap, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-20174.
Full textLyon, Alexandra Haley. "Predictors of Dropout in Clients Treated for Obsessive Compulsive Disorder with Exposure and Response Prevention." Xavier University Psychology / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=xavier1586197796058032.
Full textJackson, Stacey Anne Winifred. "Modelling the neuropsychopharmacology of obsessive-compulsive disorder in the common marmoset (Callithrix jacchus)." Thesis, University of Cambridge, 2019. https://www.repository.cam.ac.uk/handle/1810/288835.
Full textEdwards, Ethan Jack. "Personality Factors, Obsessive-Compulsive Behavior, and Sexual Fantasy as Predictors of Paraphilic Disorder Intensity." TopSCHOLAR®, 2017. https://digitalcommons.wku.edu/theses/2039.
Full textWiddifield, Colin. "Post-Secondary Students with Obsessive-compulsive Disorder: An Interpretative Phenomenological Approach Linking Persistence and Quality of Life Insights." Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/33350.
Full textKinnear, C. J. (Craig John). "Molecular genetic strategies to identify Obsessive-compulsive disorder (OCD) and schizophrenia candidate genes in a South African sub-population group." Thesis, Stellenbosch : Stellenbosch University, 2007. http://hdl.handle.net/10019.1/21666.
Full textENGLISH ABSTRACT: Obsessive-compulsive disorder is a severe, debilitating psychiatric disorder for which the underlying molecular aetiology still remains unclear. Evidence from family studies have suggested that OCD may be caused by a complex interplay of environmental and genetic factors. In order to identify the genetic factors that mediate OCD susceptibility, several genetic association studies have been undertaken, which have yielded inconsistent findings. Moreover, the majority of these studies have focused on a small number of candidate genes that encode components of the serotonin and dopamine neurotransmitter pathways. However, based on the complexity of clinical manifestations observed in OCD, it is likely that its pathogenesis is mediated by a broader complex of interrelated neurotransmitter systems and signal transduction pathways; consequently there is a need to identify and assess novel candidate genes. One method of identifying such novel OCD candidate genes is by utilising knowledge of diseases with phenomenological overlap with OCD, which lend themselves to better genetic dissection through linkage analysis and animal studies. Genetic loci for such disorders, identified though linkage analysis, could potentially harbour novel OCD candidate genes, while genes implicated through animal models may lead to the identification of additional susceptibility genes through delineation of pathways by, for instance, interactome analysis. One such disorder is schizophrenia, which manifests overlap in both symptoms and brain circuits with OCD. In schizophrenia, in addition to several case-control association studies having been performed, linkage data, studies of chromosomal aberrations and animal models have led to the identification of many chromosomal regions that may contain genes involved in its aetiology and thus may also contain OCD candidate genes. In the present investigation, this approach was employed using previously reported schizophrenia susceptibility loci to identify novel OCD candidate genes. All genes residing in each of these loci were catalogued and individually analysed using a battery of bioinformatic techniques in order to assess their potential candidature for OCD susceptibility. These analyses yielded 13 credible OCD candidate genes.Additional candidates were sought using information regarding a well-defined schizophrenia animal model, the heterozygous reeler mouse, that exhibits neurodevelopmental, neuroanatomical and behavioural abnormalities, similar to those displayed by patients with schizophrenia. The phenotype of these mice is caused by a mutation in Reln, which encodes reelin, a large extracellular matrix protein that plays a pivotal role in the ordered migration of neurons during the development of laminar brain structures. The fact that both reelin protein and mRNA levels have been shown to be reduced in post-mortem brain sections of schizophrenic patients, coupled with the observed behaviour and neurochemical similarities between the heterozygous reeler mouse and schizophrenic patients suggests that reelin may be involved in the pathogenesis of schizophrenia and hence also OCD. Furthermore, genes encoding proteins that interact with reelin may thus also be considered plausible candidate genes for both schizophrenia and OCD. For this reason, novel reelin-interacting proteins were sought using the N-terminal reeler-domain of reelin, a domain only found in proteins involved in neuronal migration, as “bait” in a yeast twohybrid screen of a foetal brain cDNA library. Putative reelin ligands were subsequently reevaluated using co-immunopreciptitation and mammalian two-hybrid analysis to corroborate the yeast two-hybrid findings. Results of these analyses showed that WDR47, a WD40-repeat domain protein, interacts with reelin via its reeler-domain; therefore, the gene encoding this ligand protein, as well as RELN itself, was also considered a credible OCD candidate gene. Each of the candidate genes identified using the afore-mentioned strategies were assessed for their potential role in the aetiology of OCD by case-control association studies of a cohort of Afrikaner OCD patients and control individuals. Statistically significant associations were detected for two genes, DLX6 and SYN3, with the disorder. These associations are exciting as they may point to novel mechanisms involved in OCD development. The identification of WDR47 as a novel reelin-interacting protein has significant implications for our understanding of reelin-dependant signalling. Using this protein as the starting point, further novel components of the reelin signalling pathway may be unravelled, an investigation which may lead to the identification of novel roles for reelin in neurodevelopment. Such novel components may, of course, also be considered OCD and schizophrenia candidate genes, which may, in turn, augment the existing knowledge of the pathophysiologies of OCD, schizophrenia and other neurodevelopmental disorders. Taken together, the current study yielded exciting results that warrants follow-up investigation in future. The identification of DLX6 and SYN3 as novel OCD susceptibility genes as well as the identification of WDR47 as a reelin-interacting protein may provide investigators with alternative avenues of research into potential pathological mechanisms involved both in OCD and schizophrenia, which may ultimately lead to alternative pharmacotherapy.
AFRIKAANSE OPSOMMING: Obsessiewe kompulsiewe steuring (OKS) is `n ernstige, verswakkende psigiatriese steuring waarvan die onderliggende molekulêre etiologie steeds onbekend is. Bewyse verkry vanuit familiestudies het voorgestel dat OKS moontlik veroorsaak word deur `n komplekse interaksie van omgewings en genetiese faktore. Om die genetiese faktore te identifiseer wat OKS vatbaarheid veroorsaak, is `n hele aantal genetiese assosiasie studies onderneem, wat teenstrydige resultate gelewer het. Wat meer is, die grootste hoeveelheid van hierdie studies het gefokus op `n klein aantal kandidaatgene wat vir komponente van die serotonien en dopamine neurotransmittor weë enkodeer. Dit is egter, gebaseer op die kompleksiteit van die kliniese manifestasies wat waargeneem word in OKS, heel moontlik dat die patogenisiteit van die siekte bemiddel word deur `n breër kompleks van interverwante neurotransmittor sisteme en seintransduksie weë. Daar is dus `n behoefte na die identifikasie en ondersoek van nuwe kandidaatgene. Een metode om sulke nuwe OKS kandidaatgene te identifiseer, is deur die gebruik van bestaande kennis oor siektes wat fenomenologiese ooreenkomste het met OKS, siektes wat makliker geneties ontleed kan word deur koppelingsanalises en dierestudies. Genetiese lokusse vir sulke versteurings, geïdentifiseer deur koppelingsanalises, het die potensiaal om nuwe OKS kandidaatgene in te sluit, terwyl gene wat geïmpliseer word deur dierestudies mag lei tot die identifisering van bykomende vatbaarheidsgene deur die ondersoek van weë deur, byvoorbeeld, interaktoom analises. `n Voorbeeld van so `n versteuring is skisofrenie, wat in manifestasie oorvleuel in beide simptome en breinstroombane met OKS. In skisofrenie het, addisioneel tot verskeie geval-kontrole assosiasiestudies wat gedoen is, koppelingsdata, studies van chromosomale afwykings en dierestudies gelei tot die identifikasie van verskeie chromosomale gebiede wat gene mag bevat wat betrokke kan wees in die etiologie van die siekte, en dus ook OKS kandidaatgene mag bevat. In die huidige ondersoek is hierdie benadering gevolg en is gebruik gemaak van voorheen gerapporteerde skisofrenie vatbaarheidslokusse om nuwe OKS kandidaatgene te identifiseer. Alle gene wat in hierdie lokusse voorkom is gekatalogiseer en individueel geanaliseer deur gebruik te maak van `n battery van bioinformatika tegnieke om hul potensiaal as kandidate vir OKS vatbaarheid te bepaal. Hierdie analise het 13 geloofwaardige OKS kandidate opgelewer. Addisionele kandidate is gesoek deur inligting van `n goed gedefinieerde skisofrenie dieremodel te gebruik, naamlik die heterosigotiese “reeler” muismodel, wat neuro-ontwikkelings-, neuroanatomiese- en gedragsabnormaliteite vertoon, soortgelyk aan dié wat voorkom by pasiënte met skisofrenie. Die feit dat daar aangetoon is dat beide reelin protein en bRNS vlakke verlaag is in post-mortem brein seksies van skisofrenie pasiënte, gekoppel aan die gedrags- en neurochemiese ooreenkomste wat gesien word tussen heterosigotiese “reeler” muise en skisofrenie pasiënte, stel voor dat reelin betrokke is by die patogenese van skisofrenie en dus ook OKS. Vir hierdie rede is nuwe proteïene gesoek wat `n interaksie met reelin toon, deur gebruik te maak van die N-terminale reeler-domein van reelin, `n domein wat slegs gevind word in proteïene wat betrokke is by neuronale migrasie, as “aas” in `n gis-twee-hibried sifting van `n fetale brein cDNS biblioteek. Vermeende reelin ligande is vervolgens herevalueer deur gebruik te maak van koimmunopresipitasie en soogdier twee-hibried analises om die gis-twee-hibried bevindings te bevestig. Resultate van hierdie analises het getoon dat daar interaksie is tussen WDR47, `n WD40-herhalingsdomein protein, met reelin via sy reeler-domein. Die geen wat hierdie ligand protein enkodeer, sowel as RELN self, is dus beskou as ‘n geloofwaardige OKS kandidaatgeen. Elkeen van die kandidaatgene wat geïdentifiseer is deur gebruik te maak van bogenoemde strategieë is ondersoek vir `n potensiële rol in die etiologie van OKS deur gebruik te maak van geval-kontrole assosiasie studies met `n groep Afrikaner OKVS pasiënte en kontrole individue. Statisties-betekenisvolle assosiasies met die versteuring is vasgestel vir twee gene, DLX6 en SYN3. Hierdie assosiasies is opwindend aangesien hul nuwe meganismes betrokke by OKS ontwikkeling mag aantoon. Die identifikasie van WDR47 as ‘n nuwe protein wat interaksie met reelin vertoon, het betekenisvolle implikasies vir die verstaan van reelin-afhanklike seining. Deur hierdie proteïn as die beginpunt te gebruik kan vêrdere nuwe komponente van die reelin seinweg ontdek word, `n ondersoek wat mag lei tot die identifisering van nuwe funksies vir reelin in neuro-ontwikkeling. Sulke nuwe komponente mag, natuurlik, ook in aanmerking kom as OKS en skisofrenie kandidaatgene, wat op sy beurt weer die bestaande kennis van die patofisiologie van OKS, skisofrenie en ander neuro-ontwikkelings versteurings mag verbreed. In samevatting, hierdie studie het opwindende resultate gelewer wat opvolgondersoeke in die toekoms regverdig. Die identifikasie van DLX6 en Syn3 as nuwe OKS vatbaarheidsgene, sowel as die identifisering van WDR47 as ‘n protein wat interaksie vertoon met reelin, mag aan navorsers alternatiewe navorsingsweë voorsien om die moontlike patologiese meganismes wat betrokke is by beide OKS en skisofrenie te ondersoek, wat uiteindelik mag lei tot alternatiewe farmakoterapie.
Beijar, Odh Maria. "När hälsa blir ohälsa : En studie om Ortorexia Nervosa och två sorters självkänsla." Thesis, Mälardalens högskola, Akademin för hälsa, vård och välfärd, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-18774.
Full textMcLean, Lisa Mae. "Local visual processing in high obsesssive compulsive disorder (OCD) scorers : [a thesis submitted to the Victoria University of Wellington in fulfilment of the requirements for the degree of Master of Arts in Psychology] /." ResearchArchive@Victoria e-Thesis, 2009. http://hdl.handle.net/10063/1023.
Full textvon, Strunck Hilmar. "Exploration of the Relationship between OCD and Parenting Style Subtypes." ScholarWorks, 2016. https://scholarworks.waldenu.edu/dissertations/2017.
Full textSimmonds, Sarah. "Obsessive compulsive disorder in children and young people : experiences of children with OCD and the involvement of families in treatment." Thesis, University of Warwick, 2009. http://wrap.warwick.ac.uk/3260/.
Full textShafran, Rosamund Lucy. "An investigation into the cognitive-behavioural model of obsessive-compulsive disorder (O.C.D.) : can this be reconciled with a neurological deficit model?" Thesis, King's College London (University of London), 1995. https://kclpure.kcl.ac.uk/portal/en/theses/an-investigation-into-the-cognitivebehavioural-model-of-obsessivecompulsive-disorder-ocd--can-this-be-reconciled-with-a-neurological-deficit-model(825d532c-226d-486e-ba58-c8f7c114f0f6).html.
Full textKartberg, Emma. "OCD and Empathy Games : Using empathy games to inform the public about ODC." Thesis, Högskolan i Skövde, Institutionen för informationsteknologi, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-17846.
Full textFox, Elena M. "Mental Illness Identity: A Look at the Self, Self-Concept, and Stigma Resistance Among Those Suffering from Obsessive Compulsive Disorder." Kent State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=kent1550592968807663.
Full textKolta, Marian. "An exploratory investigation of key clinical and neuropsychological characteristics in children and adolescents with Attention Deficit Hyperactivity Disorder (ADHD) and/or Obsessive Compulsive Disorder (OCD)." Swinburne Research Bank, 2009. http://hdl.handle.net/1959.3/66848.
Full textSubmitted in fulfillment of the requirements for the degree of Doctor of Philosophy, Faculty of Life and Social Sciences, Swinburne University of Technology - 2009. Typescript. Includes bibliographical references (p. 264-308)
Fryklund, Julia. "Tvingande tankar i skolbänken : En kvalitativ studie om hur tvångssyndrom påverkar skolgången." Thesis, Umeå universitet, Institutionen för socialt arbete, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-129432.
Full textKnopp, Jasmin. "Individual differences in response to brief psychological interventions : using a mixed methods design to identify the role of user characteristics in the treatment of Obsessive-Compulsive Disorder (OCD)." Thesis, University of Manchester, 2017. https://www.research.manchester.ac.uk/portal/en/theses/individual-differences-in-response-to-brief-psychological-interventions-using-a-mixed-methods-design-to-identify-the-role-of-user-characteristics-in-the-treatment-of-obsessivecompulsive-disorder-ocd(8e5409f1-0c2f-434e-9ba6-a0c402afbc7d).html.
Full textJohansson, Jessica, and Tony Jonsson. "Faktorer som möjliggör och hindrar aktivitetsutförande hos personer med tvångssyndrom : En litteraturstudie baserad på bloggar och självbiografi." Thesis, Luleå tekniska universitet, Hälsa och rehabilitering, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-63704.
Full textSpragg, Melanie. ""Life just kind of sparkles" : clients' experiences of being in a Cognitive Behavioural Group and its impact on reducing shame in Obsessive Compulsive Disorder (OCD)." Thesis, University of East London, 2013. http://roar.uel.ac.uk/3085/.
Full textBlanco, Hinojo Laura 1981. "Functional connectivity anomalies in the neural networks mediating motivated behavior : assessong obsessive-compulsive disorder , chronic cannabis use, Prader-Willi syndrome and Down syndrome." Doctoral thesis, Universitat Pompeu Fabra, 2015. http://hdl.handle.net/10803/328419.
Full textEls trastorns compulsius, impulsius, i addictius, mostren trets comuns associats a una disfunció en la regulació de la conducta motivada. El conjunt de xarxes neuronals que connecten àrees corticals, principalment frontals, amb els ganglis basals, té un paper rellevant a la conducta motivada. Hem utilitzat mesures de RM per avaluar l’estat funcional dels circuits corticals-ganglis basals, així com la seva interacció amb altres xarxes cerebrals, en quatre trastorns que d’una manera característica presenten alteracions de la conducta motivada. Les mostres d’estudi van incloure un grup de 74 pacients amb trastorn obsessiu-compulsiu, 28 consumidors crònics de cànnabis, 24 persones amb síndrome de Prader-Willi i 20 persones amb síndrome de Down. A més, vam utilitzar RM estructural per caracteritzar les correlacions volumètriques de substància grisa dins d’aquests mateixos circuits en subjectes sans. Els resultats mostren alteracions comunes i diferents entre els grups d’estudi, associades a la gravetat dels seus símptomes més característics. En el context específic de la fisiologia frontal-ganglis basals, les troballes poden proporcionar nous coneixements sobre la naturalesa del comportament obsessiu compulsiu, els límits amb la impulsivitat i el paper de les motivacions bàsiques no satisfetes en la gènesi de les obsessions.
Eldnes, Hilde Finstad. "Betydningen av terapeutens rolle i arbeidet med mennesker som lider av OCD : En kvalitativ studie av terapeutiske faktorer og framgangsmåter." Thesis, Karlstads universitet, Fakulteten för humaniora och samhällsvetenskap (from 2013), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-37081.
Full textPinsker, Cristina M. "The FFOCI, and Other Measures and Models of OCPD." UKnowledge, 2014. http://uknowledge.uky.edu/psychology_etds/38.
Full textLucey, James Vincent. "Regional cerebral blood flow (rCBF) assessed as uptake of '9'9'mTc-HMPAO in the basal ganglia and other brain regions in obsessive-compulsive disorder (OCD) on single photon tomography (SPET)." Thesis, Imperial College London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.392900.
Full textSilva, Elisabeth Meyer da. "Efeitos da entrevista motivacional e do mapeamento cognitivo associados à TCCG no tratamento de pacientes com transtorno obsessivo-compulsivo." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2009. http://hdl.handle.net/10183/25116.
Full textINTRODUCTION According to the Diagnostic and Statistical Manual of Mental Disorders (DSMIV; American Psychiatric Association, 2002), Obsessive-compulsive disorder (OCD) is characterized by recurrent obsessions and/or compulsions that significantly interfere with daily functioning. Although group cognitive behavioral therapy (GCBT) has been effective for OCD patients (Cordioli et al., 2003; Braga et al., 2005; Sousa et al., 2006), almost onethird (30%) of patients did not benefit from this treatment. Motivational Interviewing (MI) and Thought Mapping (TM) have been used to enhance treatment outcome. AIMS The main goal of the present study was to examine the effects of adding individual sessions of MI and TM to 12 weeks of CBGT on the treatment outcome of OCD patients when compared to the CBGT alone. METHODS Ninety-three adult outpatients, with OCD diagnosis according to the DSM-IV participated in a 14-week randomized clinical trial: 48 patients were allocated to two individual sessions of MI+TM in addition to 12-week CBGT; 45 underwent two individual information sessions followed by CBGT. For the outcomes evaluation, the Yale-Brown Obsessive Compulsive Scale (YBOCS) was used as the primary efficacy measure. As secondary efficacy measures, the Clinical Global Impressions Scale (CGI), the Beck Depression Inventory (BDI) and the proportion of responders (defined as improved [reduction 35% on the Y-BOCS] or non-improved [reduction 35% on the Y-BOCS]) and the percentage of patients in partial remission (Y-BOCS 35% but with the total score >8 and CGI 2) and full remission (Y-BOCS 8 and CGI < 2) were used. RESULTS When the two groups were compared, both presented a reduction of OCD symptoms. However, symptom reduction and remission were significantly higher in the MI+TM CBGT group. In addition, positive outcomes were maintained at the 3-month follow-up with additional symptom reduction. CONCLUSION This study is the first randomized clinical trial which adds individual sessions of MI+TM to CBGT to improve the outcome of group treatment for OCD. Despite some limitations, our results suggest that adding MI+TM to CBGT can enhance the CBGT effectiveness in reducing OCD symptoms. Future studies should investigate the effect of the MI and the TM alone as an augmentation strategy for OCD treatment.
Robinson, Kelsey M. "Is the Fixation on “Healthy” Unhealthy? A Study on Orthorexia Nervosa." Kent State University Honors College / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ksuhonors1315880914.
Full textBation, Rémy. "Stimulation électrique par courant continu (tDCS) dans les Troubles Obsessionnels et Compulsifs résistants : effets cliniques et électrophysiologiques." Thesis, Lyon, 2018. http://www.theses.fr/2018LYSE1344/document.
Full textObsessive-compulsive disorder (OCD) is a severe mental illness. OCD symptoms are often resistant to available treatments. Neurobiological models of OCD are based on an imbalance between the direct (excitatory) and indirect (inhibitory) pathway within this cortico-striato-thalamo-cortical loops, which causes hyperactivation in the orbito-frontal cortex, the cingular anterior cortex, the putamen. More recently, the role of cerebellum in the OCD physiopathology has been brought to light by studies showing structural and functional abnormalities. We proposed to use tDCS as a therapeutic tool for resistant OCD by targeting the hyperactive left orbito-frontal cortex with cathodal tDCS (assumed to decrease cortical excitability) coupled with anodal cerebellar tDCS. In a first study, we studied the feasibility of this treatment protocol in an open-trial. This study found a significant reduction in symptoms in a population with a high level of resistance. In a second study, we evaluated the effect of this treatment in a randomized-controlled trial. This study did not confirm the effectiveness of this intervention. We have assessed motor cortex cortical excitability parameters by transcranial magnetic stimulation. We thus demonstrated that the tDCS caused a significant increase of inhibition processes (Short Interval Cortical Inhibition: SICI) and a nonsignificant decrease in the facilitation processes (Intra Cortical Facilitation (ICF)). In addition, clinical improvement assessed by Clinical Global Impression at the end of the follow-up period (3 months) was positively correlated with SICI at baseline.tDCS with the cathode placed over the left OFC combined with the anode placed over the right cerebellum decreased hyper-excitability in the motor cortex but was not significantly effective in SSRI- resistant OCD patients. These works were discussed in light of the available literature to create future prospect in the field of tDCS treatment for OCD resistant patients
Adut, Sarah Lily. "Looking Outside of Self and Experience: Effects of Cognitive Distancing on Intrusive Thought Responses." Miami University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=miami1578603833148252.
Full textWolmarans, Petrus De Wet. "Stereotypical behaviour in the deer mouse (Peromyscus Maniculatus bairdii) : a pharmacological investigation of the frontal–cortico–striatal serotonergic system / Wolmarans D." Thesis, North-West University, 2011. http://hdl.handle.net/10394/7585.
Full textThesis (M.Sc. (Pharmacology))--North-West University, Potchefstroom Campus, 2012.