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Thesis (M.A. (Clinical Psychology)) --University of Limpopo, 2008 / The aim of this study was to investigate the psychological difficulties encountered and ways of coping by HIV/AIDS orphans in Limpopo Province. The sample was comprised of 70 children whose parent(s) died of HIV/AIDS related diseases between the ages 05 and 18 years. The data were collected through the use of face to face interview and questionnaires. The study results show that as a results of trauma resulting from taking care and witnessing ill parent(s) die, HIV/AIDS orphans suffer from sadness, helplessness, anger, guilty, aggression and frustration that often lead to withdrawal and subsequent depression, In quantitative study Beck Depression Inventory was also used to determine the levels of depression (mild, moderate, and/or severe levels) and it was discovered that HIV/AIDS orphans experience moderate to severe depression. The study further looked on whether demographic factors including (age, gender, religion, home language, number of siblings, and level of education) have an impact on the experience of depression. Qualitative study findings also discovered that HIV/AIDS orphans do not experience the relationship with their caregivers as being supportive. Furthermore, mixing with non-orphaned peers was reported to be a mission and emotionally distressing. Qualitative study also discovered that HIV/AIDS orphans lack many adults whom they can trust and who they could be able to express their feelings, as result they try to find their own ways of coping with their circumstances. However, quantitative study also looked at three ways of coping (cognitive, behavioural and avoidance ways of coping) that could be used by HIV/AIDS orphans. This was achieved through the use of ways of coping scales. The findings of this study discovered that HIV/IADS orphans use cognitive and avoidance ways of coping more than behavioural ways of coping. Furthermore, the study looked at whether there is a relationship between ways of coping and biographic factors (age, gender, religion, home language, number of siblings, and level of education). It was discovered that HIV/AIDS orphans are psychologically distressed and need to be transferred for psychological therapy after the loss of their parents.

It is of crucial importance to identify and disseminate effective treatments for paediatric obsessive-compulsive disorder (OCD). OCD is time-consuming and distressing, and can substantially disable functioning at school, at home, and with peers (Piacentini, 2003). Children who do not receive treatment are at risk of psychological difficulties in adulthood, including continued OCD, clinical anxiety and depression, personality disorders, and social maladjustment (Wewetzer et al., 2001). Two-thirds of adult cases of OCD develop in childhood, and adults with OCD have lower employment, poorer academic achievement, and lower marital rates compared to non-OCD adults (Hollander et al., 1996; Koran, 2000; Lensi et al., 1996; Steketee, 1993). The distressing nature of OCD in childhood, accompanying psychosocial impairment and risk of future psychopathology, underscore the need to identify effective treatments. The primary aim of this thesis was to expand knowledge of evidence-based treatments for paediatric OCD. A mixed-methodology approach was employed to examine key issues in this area. The first study used meta-analytic methodology to determine the evidence supporting available treatments for paediatric OCD. An extensive literature search revealed over 100 published reports of treatments, encompassing a broad array of theoretical approaches and treatment strategies. Examples of treatments used for paediatric OCD included psychodynamic therapy, pharmacotherapy, cognitive-behavioural therapy (CBT), hypnosis, family therapy, immunotherapy, and homeopathy. / Study 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.

Les difficultés psychologiques sont parfois difficiles à évaluer au cours d'une consultation médicale par un non professionnel (psychologue, psychiatre). Ceci est d'autant plus vrai dans le cas particulier des jeunes enfants lors d'interventions humanitaires, ce qui conduit souvent à une réponse insuffisante aux besoins de soins psychiques. Le manque d'outils validés de manière transculturelle qui répondent aux exigences d'intervention, rapide et simple pour identifier les besoins combinés à un manque de professionnels impliquent des difficultés voire l'impossibilité de mettre en place les prises charges adéquates. Dans ce travail, nous avons réalisé la validation transculturelle d'un outil de dépistage des difficultés psychologiques en contexte humanitaire destiné aux enfants âgés de 3 à 6 ans, le PSYCa 3-6 (Psychological Screening tool for Young Children aged 3 to 6). Cet outil a été initialement créé et développé en 1999 lors d'une intervention humanitaire, son contenu a été affiné et modifié au fur et à mesure de son utilisation. La validation principale a eu lieu au Niger, et deux validations complémentaires ont été mises en place en Colombie et au Kenya. Au total, 888 enfants âgés de 3 à 6 ans ont été inclus entre Octobre 2009 et Février 2012. Une recherche qualitative a été mise en place en amont de la validation pour collecter des informations concernant la perception des difficultés psychologiques localement au Niger. La recherche quantitative s'est intéressée aux qualités psychométriques et cliniques de l'outil. Les trois versions haoussa, espagnole et swahili ont montré des qualités psychométriques et cliniques adéquates incluant une bonne validité concurrente, les scores obtenus à l'outil étant corrélés au gold standard. La recherche qualitative a permis d'affiner et de renforcer les résultats. A notre connaissance, il s'agit de la première validation d'un outil de dépistage pour des enfants d'âge préscolaire incluant un volet transculturel pour usage dans des contextes humanitaires variés. De tels outils validés pour des contextes différents sont indispensables pour promouvoir l'accès aux soins psychiques pour les enfants, souvent non prioritaires dans ces interventions. / Psychological difficulties are sometimes difficult to assess during a medical consultation by a non-specialist (psychologist, psychiatrist). This is especially the case when it comes to young children, in humanitarian intervention contexts, entailing an insufficient answer to the needs of mental health care. The lack of cross culturally validated tools that meet the requirement of such intervention, fast and simple to identify the needs combined with a lack of professional involve difficulties even impossibility of implementing appropriate care. In this study, we implemented a cross cultural validation of a screening tool for psychological difficulties in humanitarian context for children aged 3 to 6 years old, the PSYCa 3-6 (Psychological Screening tool for Young Children aged 3 to 6 years old). This tool was originally created and developed during a humanitarian intervention; its content has been refined and modified along its use. The main validation took place in Niger, and two additional validations have been implemented in Colombia and Kenya. In total, 888 children aged 3 to 6 years were recruited between October 2009 and February 2012. Qualitative research has been also implemented to collect information regarding the local perception of psychological difficulties, prior to the validation. Quantitative research has focused on the psychometric and clinical properties of the tool. The three versions, Hausa, Spanish and Swahili showed adequate psychometric and clinical qualities including a good concurrent validity, scores being correlated with the gold standard. Qualitative research was used to refine and to strengthen the results. To our knowledge, this is the first validation of a screening tool for preschool children including a cross cultural component for use in several humanitarian contexts. Such tools, cross culturally validated in several contexts, are a key component to promote access to mental health care for children, often not on the list of priorities during the interventions.

The aim of this work is to describe hagiotherapy as a suitable psychoterapic method for work with psychological difficulties of workers in helping professions. The first chapter is dedicated to the hagiotherapy description, its development, selected philosophical solutions, its procedure and targeted groups in which the hagiotherapy is applied. The second chapter is dedicated to psychical difficulties of workers in helping professions and is focused on the following phenomena: helper syndrome, power in helping professions, burnout syndrome. The third chapter reveals the authorś assumptions, the reasons why she considers the hagiotherapy a suitable supporting means for workers in helping professions. In the fourth chapter an illustrative investigation is presented which is supposed to answer the question: What impact did the hagiotherapy have in the life of worker in helping professions? This question was answered by the participants of the illustrative investigation, who are workers in helping professions and completed hagiotherapy trainings. For the analysis of their answers in the illustrative investigation the elements of grounded theory were used.