INTRODUCTION: The rate of smoking is significantly higher among people living with HIV (PLWH) in comparison to the general population (CDC, 2017b; Humfleet et al., 2009). Tobacco use among PLWH heightens the risk for HIV-related symptoms and is a pertinent public health issue. Smokers living with HIV are also more likely to develop non-AIDS-related illness in comparison to non-smokers living with HIV. Smoking cessation interventions are desperately needed to cater towards PLWH. This warrants the need for patient-provider interactions in healthcare facilities regarding smoking cessation. AIM: To document rates of smoking and visitations to healthcare facilities among persons living with and without HIV in higher vs. lower-risk areas and to examine associations among healthcare visitations, stressors, and smoking in these sub-samples (i.e., PLWH in higher-risk areas, PLWH in lower-risk areas, people without HIV in higher-risk areas, people without HIV in lower-risk areas). METHODS: Secondary analyses were conducted using data from a network-based, HIV endemic study that was conducted in Metro Atlanta (Rothenberg, Dai, Adams & Heath, 2017). The study included 927 participants from 10 Atlanta zip codes (5 lower-risk and 5 higher-risk based on reported HIV cases). Participants provided information on their smoking status and healthcare visitations, as well as whether they had experienced several stressors (e.g., violence, homelessness, being threatened with a weapon, lack of transportation). Descriptive analyses and frequency distributions were conducted and presented on key variables. Logistic regression analyses were conducted to examine associations between key variables and smoking. RESULTS: Overall, the rate of smoking was quite high in this study. Seventy-four percent of the sample smoked, which is almost five times the smoking rate among the general adult U.S. population (CDC, 2016a). The smoking rate was strikingly high among PLWH in the higher-risk areas (95%). In unadjusted analyses, participants who were older, male, homeless, and do not drive their own car were more likely to smoke. In the adjusted analyses age, gender, and lack of transportation remained significant predictors of smoking. Visitations to healthcare facilities were not significantly associated with smoking or other variables in this study. DISCUSSION: Smoking appears quite common among PLWH, especially those living in higher-risk areas. This study provided important information on the extent to which persons living with and without HIV in higher and lower-risk areas of Atlanta are receiving healthcare services, as well as how demographic factors and stress relate to smoking in these sub-samples. Future research is needed to develop and disseminate effective smoking cessation programs among smokers living with HIV.

Abstract Throughout history, many diseases have carried considerable stigma, including leprosy tuberculosis, cancer, mental illness and many STDs. Now HIV/AIDS is the topmost in the list of diseases that leads to devastating patient stigmatization. Despite international efforts to tackle HIV/AIDS, stigma and discrimination remain among the most poorly understood aspects of the epidemic. In the face of numerous intervention strategies, HIV/AIDS continues to spread and to pose a threat to the socio-economic transformation of South Africa. The broad objective of this study was to investigate how the stigmatisation of HIV-Positive women is made manifest and look at how successful the National Association of people living with HIV/AIDS (NAPWA) in South Africa has been in achieving their objectives and goals of changing the perceptions people have about HIV/AIDS and creating awareness about the debilitating effect stigmatisation has in the society, especially when it viciously targets HIV-positive women. A case study approach was used to examine the experiences of HIV/AIDS infected/affected women and NAPWA administrators. Methods used in the collection of data were self-administered questionnaires, participant observation and archival evidence in the form of documents. Through these methods, the study investigated ways in which the stigmatisation of HIV-positive women was made manifest, the role of NAPWA in fighting HIV/AIDS stigmatisation, how successful NAPWA has been in the fight against the stigmatisation of people infected and affected by HIV/AIDS in South Africa, challenges faced by NAPWA in the fight against HIV stigmatisation and discrimination, weaknesses of NAPWA and what impact all these have in the spread of HIV/AIDS. The research results show that HIV-positive women suffer stigmatisation and that; organisations of people living with HIV/AIDS (e.g. NAPWA-SA) play a major role in eradicating the stigma attached to HIV/AIDS. It also suggests that APWAs in effect help to reduce the spread of the disease and prolong the life span of those infected by it. All this not withstanding, the study also discovered that APWAs like NAPWA-SA need the support of government and stakeholders in South Africa to fully implement their strategies and programmes geared towards reducing stigma and the spread of HIV/AIDS.

Thesis (MPH)--University of Limpopo, 2011. / Background: Support groups are an informal resource that attempts to provide healing components to a variety of problems and challenges. An informal support outside of family, friends, or professionals often provides greater understanding, more similarity (from individuals experiencing similar life events), an opportunity for empathy and altruism, and a sense of identity for participants. Learning new ways to handle challenges, cope with changes, and maintain new behaviors are all important aspects of the support group experience. Purpose: The aim of the study was to determine what HIV positive people perceive as barriers to participate in HIV support groups. Methods: This was a quantitative study design using structured questionnaires on 248 participants who gave written consents to participate in the study. Results: Majority were female 63% participants, single (52.63%), unemployed (60%), between ages 31-40 and 52.02% attained secondary education. Participants who were currently on HIV treatment (prophylaxis and ARV) has attended HIV support groups before while participants who were not on any treatment have never attended HIV support groups. Participants who never attended HIV support group also never attended other support groups. The main reasons that participants gave for not attending in HIV support groups was that they are concerned about their privacy and HIV status being known by others. Barriers preventing attendance of HIV support group were support groups are hard to find, work schedules and lack of transport money.

No abstract available. / Dissertation (LLM)--University of Pretoria, 2013. / gm2014 / Centre for Human Rights / unrestricted

The lifetime prevalence of clinical depression in patients living with human immunodeficiency virus/acquired immune deficiency syndrome (HIV/AIDS) is approximately 22% compared to 3% to 10% in the primary care population. The nursing practice problem at the project site concerned nurses' lack of knowledge and understanding of procedures to help ensure that all patients living with HIV/AIDS were properly screened for depression and referred for further evaluation and treatment. The purpose of this project was to implement a staff education module to address the use of the PHQ-9 screening tool to identify depression in people diagnosed with HIV/AIDS. The theoretical framework for this educational module was the theory of planned behavior. The practice-focused question explored the extent to which the implementation of an evidence-based practice education model in a primary care clinic treating patients living with HIV/AIDs would increase staff knowledge on the use of the PHQ-9 tool to screen for depression. A staff education project incorporating a pretest and posttest design was conducted to determine whether a significant change existed in the test scores of the participants between the pretest and the posttest. After completion, the posttest measures showed an improvement of 35%. The implications of this project for social change might include improvement in the knowledge, attitudes, and practices of the nurses in the treatment of depression in adults living with HIV/AIDS.

Thesis (M.A. (Clinical psychology) --University of Limpopo, 2009. / The study aimed at assessing and understanding the unmet needs and well-being among people living with HIV/AIDS. People living with HIVAIDS experience many challenges. Challenges may be characterized by medical, social and psychological challenges. Method: A cross sectional design was used. A total of (N = 200) young and adult age ranged from 20-71 years ( = 43.70, SD = 12.420) women (62%) and 75 men (37, 5%) living with HIV/AIDS who attend HIV/AIDS clinic/unit in Polokwane/Mankweng hospital complex was selected with purposive sample. Results: Four hypotheses were tested with one-way ANOVA. The findings indicated that social support (p < .001) and age (p < .04) plays a significant role in the psychological well-being of people living with HIV/AIDS. Medical challenges and gender revealed no significant results. Conclusion: It is concluded that PLWHA attend some form of support groups which will aid in alleviating the psychological distress associated with HIV/AIDS.

No description available.

High levels of HIV stigma are reported for people living with HIV or AIDS (PLHA) and PLHA have to cope with this. These experiences may differ in a rural and urban setting. Obtaining a true reflection of the level of HIV stigma experienced by PLHA in a rural and urban setting and their level of coping self-efficacy, while dealing with this stigma, will be helpful in planning future intervention strategies. The study aims to compare qualitative expressed experiences with quantitative measures of levels of HIV stigma and coping self-efficacy of PLHA in a rural and urban setting. Secondly the aim is to establish the relationship between the levels of HIV stigma experiences of PLHA and coping self-efficacy of PLHA. The study took place in the North West Province, in both a rural (n=12) and urban (n=11) setting. Participants were selected by means of purposive sampling. A convergent parallel design was used within a mixed method approach. In-depth interviews provided qualitative data. Quantitative data came from two scales, the HIV and AIDS stigma scale-PLWA (HASI-P) (Holzemer et al., 2007a) and the Coping self-efficacy scale (CSE) (Chesney, Neilands, Chambers, Taylor, & Folkman, 2006). The study revealed that HIV stigma does exist, and is experienced by PLHA in the North West province in both a rural and an urban setting with no significant difference. Qualitative data confirmed the results of the HIV stigma measure, and also provided a rich understanding of the differences in contexts between the two settings. Additional types of stigma found to those included in the HASI-P point to shifts in the way people and communities experience HIV stigma. Results of the CSE scale showed that PLHA from both rural and urban settings employed the three types of coping self-efficacy as described by Chesney et al. (2006), with no significant difference between the two groups. Statistical correlations within the HASI-P revealed correlations between certain types of stigma experienced, indicating that HIV stigma is not experienced in a single dimension but can extend to more than one area of the lives of PLHA. Correlations within the CSE scale illustrate that ways PLHA cope may be related to each other Recommendations focus on further research options, policy development and implementation in practice. The goals of the research were reached in that it was confirmed that HIV stigma and coping self-efficacy of PLHA in rural and urban settings, using qualitative and quantitative methods, does exist. The relationship between HIV stigma and coping self-efficacy of PLHA was established through the correlation of scales and through the evidence found during in-depth interviews; that HIV stigma exists and that PLHA develop coping self-efficacy to deal with it. / Thesis (MA (Research Psychology))--North-West University, Potchefstroom Campus, 2013

High levels of HIV stigma are reported for people living with HIV or AIDS (PLHA) and PLHA have to cope with this. These experiences may differ in a rural and urban setting. Obtaining a true reflection of the level of HIV stigma experienced by PLHA in a rural and urban setting and their level of coping self-efficacy, while dealing with this stigma, will be helpful in planning future intervention strategies. The study aims to compare qualitative expressed experiences with quantitative measures of levels of HIV stigma and coping self-efficacy of PLHA in a rural and urban setting. Secondly the aim is to establish the relationship between the levels of HIV stigma experiences of PLHA and coping self-efficacy of PLHA. The study took place in the North West Province, in both a rural (n=12) and urban (n=11) setting. Participants were selected by means of purposive sampling. A convergent parallel design was used within a mixed method approach. In-depth interviews provided qualitative data. Quantitative data came from two scales, the HIV and AIDS stigma scale-PLWA (HASI-P) (Holzemer et al., 2007a) and the Coping self-efficacy scale (CSE) (Chesney, Neilands, Chambers, Taylor, & Folkman, 2006). The study revealed that HIV stigma does exist, and is experienced by PLHA in the North West province in both a rural and an urban setting with no significant difference. Qualitative data confirmed the results of the HIV stigma measure, and also provided a rich understanding of the differences in contexts between the two settings. Additional types of stigma found to those included in the HASI-P point to shifts in the way people and communities experience HIV stigma. Results of the CSE scale showed that PLHA from both rural and urban settings employed the three types of coping self-efficacy as described by Chesney et al. (2006), with no significant difference between the two groups. Statistical correlations within the HASI-P revealed correlations between certain types of stigma experienced, indicating that HIV stigma is not experienced in a single dimension but can extend to more than one area of the lives of PLHA. Correlations within the CSE scale illustrate that ways PLHA cope may be related to each other Recommendations focus on further research options, policy development and implementation in practice. The goals of the research were reached in that it was confirmed that HIV stigma and coping self-efficacy of PLHA in rural and urban settings, using qualitative and quantitative methods, does exist. The relationship between HIV stigma and coping self-efficacy of PLHA was established through the correlation of scales and through the evidence found during in-depth interviews; that HIV stigma exists and that PLHA develop coping self-efficacy to deal with it. / Thesis (MA (Research Psychology))--North-West University, Potchefstroom Campus, 2013

Magister Artium (Child and Family Studies) - MA(CFS) / HIV patients face an array of social and psychological problems, such as depression, which can affect their quality of life. Moreover, HIV infection is also linked to psychological distress such as anxiety. In addition, avoidant emotion-focused strategies such as acceptance, wishful thinking and self-blame are associated with higher levels of psychological distress in persons with HIV. Current health services in the city of Cairo, Egypt, are not adapted to provide advice and psychological support to people living with HIV to aid in the development of problem-solving skills to cope with the stress of living with HIV. The purpose of this study was to examine the relationship between quality of life, psychological distress and the coping strategies of persons living with HIV/AIDS in Cairo, Egypt. A quantitative methodology with a cross-sectional correlational design was adopted in this study. Data collection entailed questionnaires that consisted of four sections: Demographics, Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q), Depression, Anxiety, Stress Scales (DASS) and the Cope Inventory. The sample consisted of 202 HIV/AIDS participants who access the National AIDS Program (NAP). The data were analysed using the Statistical Program for Social Science V23 (SPSS). The results are provided using descriptive and inferential statistics. The findings of the study show that in terms of the prevalence of psychological distress, the moderate scales were stress and depression, while the severe scale was anxiety. The most prevalent of coping styles was emotion-focused coping, specifically in terms of acceptance and religion. In terms of the prevalence of quality of life, the highest scores were for family and social relationships, while the lowest scores were for sexual drive and leisure time activities. The findings also show that psychological distress and certain coping styles such as substance use negatively predicted quality of life of patients with HIV/AIDS. Positive predictors included coping styles such as venting, positive reframing, humour, acceptance and religion.