scholarly journals The Impact of a Social Assistance Program on the Quality of Life of Older People in Uganda

SAGE Open ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 215824402198931
Author(s):  
Ivan Byaruhanga ◽  
Jonas Debesay

This study explores the impact of social assistance on older persons’ quality of life in a Ugandan district. The purpose of the study is to establish how older persons aged above 65 years provide their livelihood in the wake of declining and waning informal family/clan/society support systems. These systems have been the source of their care for a long time. The study therefore examines how the recipients of the grant manage their everyday life amid changing norms in reciprocal care. The study is based on two focus group discussions with 13 older grant beneficiaries and four in-depth interviews with key participants affiliated with the social assistance scheme. The study’s main results include themes such as fulfilling basic needs, start-up capital and credit worthiness, supplementary income, and respite from isolation and loneliness. The study shows positive changes in the lives of older persons and a notable relative improvement in the standards of living of older persons in beneficiary districts.

Pneumologia ◽  
2019 ◽  
Vol 68 (3) ◽  
pp. 107-113
Author(s):  
Beatrice Mahler ◽  
Alina Croitoru

Abstract Tuberculosis (TB) is still a leading cause of morbidity and mortality worldwide. The impact on patient’s life is significant, leading to physical, mental and social deconditioning, not only in active TB but also in post TB sequela. Although with specific antituberculous treatment sputum negativity can be achieved, TB extrapulmonary symptoms such as cachexia, muscle weakness and depression may persist for a long time. The pulmonary rehabilitation (PR) may be a useful tool in this patient’s therapy in active and also in sequela phase. The benefits of PR are: reducing symptomatology, improving the degree of functional independence and quality of life, and increasing the ability to perform daily activities. This article discusses the components of a PR programme in active TB and TB sequela, and the results obtained by studies so far.


2017 ◽  
Vol 1 (1) ◽  
pp. 53-64 ◽  
Author(s):  
Sandra Edmonds Crewe

Background: Gentrification is impacting urban communities across the globe. Some urban communities have undergone major displacement of longtime residents thus placing older persons at particular risk of social isolation and the loss of social networks. Objective: The objective of the article is to bring attention to the impact of gentrification on communities and specifically addresses the impact on older persons, especially as it relates to displacement, social isolation, and social networks. Additionally the article aims to address implications for social work practice. Method: A review of the literature was used to gather information on this important topic. Additionally, newspaper articles were reviewed that discussed gentrification in urban neighborhoods. Content analysis was used to gather themes that would inform practice recommendations. Additionally the author used community mapping through personal observation. Findings: Gentrification is perceived as both positive and negative, depending on the stakeholder. It also has been associated with negative health effects as well as social isolation and the loss of social networks. Older persons of color are particularly at risk of displacement. Emotional and financial hardships. Conclusions: Practice implications include an examination of quality of life factors, introduction of financial counseling and advocacy for policies that respect the quality of life of older persons faced with gentrification.


2020 ◽  
Vol 19 (1) ◽  
Author(s):  
Barbara Pesut ◽  
Wendy Duggleby ◽  
Grace Warner ◽  
Paxton Bruce ◽  
Sunita Ghosh ◽  
...  

Abstract Background Volunteer navigation is an innovative way to help older persons get connected to resources in their community that they may not know about or have difficulty accessing. Nav-CARE is an intervention in which volunteers, who are trained in navigation, provide services for older persons living at home with chronic illness to improve their quality of life. The goal of this study was to evaluate the impact of Nav-CARE on volunteers, older persons, and family participating across eight Canadian sites. Methods Nav-CARE was implemented using a knowledge translation approach in eight sites using a 12- or 18-month intervention period. A mixed method evaluation was used to understand the outcomes upon older person engagement; volunteer self-efficacy; and older person, family, and volunteer quality of life and satisfaction with the intervention. Results Older persons and family were highly satisfied with the intervention, citing benefits of social connection and support, help with negotiating the social aspects of healthcare, access to cost-effective resources, and family respite. They were less satisfied with the practical help available for transportation and errands. Older persons self-reported knowledge of the services available to them and confidence in making decisions about their healthcare showed statistically significant improvements (P < .05) over 12–18 months. Volunteers reported satisfaction with their role, particularly as it related to building relationships over time, and good self-efficacy. Volunteer attrition was a result of not recruiting older persons in a timely manner. There was no statistically significant improvement in quality of life for older persons, family or volunteers from baseline to study completion. Conclusions Findings from this study support a developing body of evidence showing the contributions volunteers make to enhanced older person and family well-being in the context of chronic illness. Statistically significant improvements were documented in aspects of client engagement. However, there were no statistically significant improvements in quality of life scores even though qualitative data illustrated very specific positive outcomes of the intervention. Similar findings in other volunteer-led intervention studies raise the question of whether there is a need for targeted volunteer-sensitive outcome measures.


2019 ◽  
Vol 26 (4) ◽  
Author(s):  
N. Lightfoot ◽  
L. MacEwan ◽  
L. Tufford ◽  
D. L. Holness ◽  
C. Mayer ◽  
...  

Background In the present study, we investigated the emotional, physical, financial, occupational, practical, and quality-of-life impacts on caregivers of patients with mining-related lung cancer.Methods This concurrent, embedded, mixed-methods study used individual in-depth qualitative interviews and the 36-item Short Form Health Survey (version 2: RAND Corporation, Santa Monica, CA, U.S.A.) quality-of-life measure with 8 caregivers of patients with suspected mining-related lung cancer who had worked in Sudbury or Elliot Lake (or both), and sometimes elsewhere. Individuals who assist workers in filing compensation claims were also interviewed in Sudbury and Elliot Lake. Interviews (n = 11) were transcribed and analyzed thematically.Results Caregiver themes focused on the long time to, and the shock of, diagnosis and dealing with lung cancer; not much of a life for caregivers; strong views about potential cancer causes; concerns about financial impacts; compensation experiences and long time to compensation; and suggestions for additional support. Quality-of-life scores were below the norm for most measures. Individuals who assist workers in preparing claims were passionate about challenges in the compensation journey; the requirement for more and better family support; the need to focus on compensation compared with cost control; the need for better exposure monitoring, controls, resources, and research; and job challenges, barriers, and satisfaction.Conclusions Caregivers expressed a need for more education about the compensation process and for greater support. Worker representatives required persistence, additional workplace monitoring and controls, additional research, and a focus on compensation compared with cost control. They also emphasized the need for more family support.


2013 ◽  
Vol 25 (5) ◽  
pp. 723-736 ◽  
Author(s):  
Steve La Grow ◽  
Polly Yeung ◽  
Andy Towers ◽  
Fiona Alpass ◽  
Christine Stephens

2017 ◽  
Vol 127 (1) ◽  
pp. 24-27
Author(s):  
Monika Szkultecka-Dębek ◽  
Mariola Drozd ◽  
Marta Bem

Abstract Introduction. The term “quality of life” has been present in the literature for a long time now. It was created in the middle of the last century in Western Europe and from the societal perspective the term initially defined the level of material life, gradually being expanded to other aspects of human life, like happiness, education, broadly defined individual freedom and health. Aim. To analyze differences by gender and place of residence in perception of quality of life based on data from the assessment of thrombocytopenia impact on daily activities using TSIDAV vignette among Polish patients. Material and methods. We assessed the impact of thrombocytopenia symptoms on patients’ daily activities using TSIDAV vignette. We wanted to understand the reason for different perception of symptoms and why visible symptoms are perceived as worse by women in comparison to men. We analyzed the groups by age and place of residence. Results. Within 48 collected questionnaires, 31 were provided by women and 17 by men. As many as 29% of men declared the biggest impact on daily activities due to petechiae and easy bruising. The same symptoms were assessed as having significant impact on daily activities by 68% and 65% of women respectively. The results in relation to the two symptoms were similar in terms of impact: both men and women assessed it as high impact, however in general, a lower proportion of men identified this as an issue. As many as 53% of the pre-menopausal women declared the thrombocytopenia impact on daily activities as very high. Similar results were observed in the male group. Those before retirement age assessed disease symptoms as very high in comparison to the group of older patients. No significant differences in relation to place of residence were observed. During literature research we found that depending on patients’ gender, the perception of the impact of disease on patients quality of life may often differ. Conclusions. We found out that the perception of disease symptoms impact on quality of life is different by women and men. That may be the result of different factors such as the influence of social roles determined for each sex. At the same time, the perception of the impact of thrombocytopenia symptoms on daily activity almost does not depend on age or place of residence of neither women nor men.


Author(s):  
Cícero Allan Barbosa Soares ◽  
Ian Henrique Teles Braga ◽  
Rômulo Pereira de Almeida ◽  
Marcus Vinicius De Oliveira Brasil ◽  
Paulo Renato Alves Firmino ◽  
...  

The quality of life underlying the modern society can be attributed to several factors, among them, the technological and economic development experienced in recent years. Durable consumer goods are part of this modern society, such as automobiles. However, because most automobiles are powered by the combustion of fossil fuels, the emission of greenhouse gases is a worrisome environmental problem. The objective of this article is to analyze Gross Domestic Product (GDP) data, population and SELIC rate (SELIC stands for Special System of Settlement and Custody) in the period from 2001 to 2020 to evaluate the impact on the number of vehicles in the Cariri Metropolitan Region (RMC), using multivariate models. It was verified that the fleet of the RMC experienced an increase of 561.45% in the last 20 years. Three prediction models were tested and the conclusion was reached that for the next 20 years it is not sustainable to maintain the same growth already experienced, in a linear manner. Instead, the ideal is to adopt a model with growth forecast with a logarithmic function, i. e. with a stationary tendency in the long time. In a society where over 50% of vehicles are more than 10 years old, it is essential that public managers, the private initiative, the academic-scientific environment and society adopt sustainable practices and consider future scenarios to make decisions in order to preserve the environment and to ensure everyone's quality of life.


2019 ◽  
Vol 2 (4) ◽  
pp. 143-149
Author(s):  
C.A. Verdeja-Robles ◽  
C.E. Velazquez-De la Rosa ◽  
A. Gutiérrez-Morgas

Abstract Objective: to know the prevalence of depression in patients with moderate-severe acne vulgaris. Hypothesis: the incidence of depression increases in patients with moderate-severe acne vulgaris and will therefore decrease the quality of life. Background: acne is a very frequent dermatosis in the outpatient clinic, it is not considered a life-threatening disease. It has been associated with negative emotional status. Also, suffering from it for a long time has been associated with depression, anxiety and frustration. The complications of acne in the psychosocial aspect are related to academic or vocational performance, self-esteem and adolescents’ quality of life. Materials and Methods: the type of study was retrospective cross-sectional descriptive observational study. The sampling was carried out at the facilities of the Popular Autonomous University of the State of Puebla, taking into account any person within the institutional organisation within the range of 12-20 years of age, with a total of 50 participants. The Hamilton assessment scale of depression and the Cardiff Acne disability index were applied to all patients with dermatological diagnosis of moderate-severe vulgar acne in a period between February-October 2019. Results: a total of 50patients were analysed, of which 28 were women aged 12 to 20 years and 22 men (28 women and 13 men) and severe acne in 9 patients, all over 17 years of age and male. According to the degree of depression, 28% (n = 14) of the patients were obtained without some degree of depression; 60% (n = 30) with minor depression; 12% (n = 6) with moderate depression. Regarding the quality of life: 40% (n = 20) of the patients showed good quality of life, 46% (n = 23) regular quality of life and 14% (n = 7) showed poor quality of life. Conclusion: orderly study of the psychic impact of acne and other skin diseases on people suffering them is recent and is carried out through questionnaires that try to measure the impact the diseases have on the patients’ quality of life.


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