To Join Or Not To Join? A Case Of Sickle Cell Clubs, Stigma And Discrimination In Secondary Schools In Butambala District, Uganda

IF 1.7 Q2 PEDIATRICS
Sharifu K Tusuubira, Tracy Naggawa, Victoria Nakamoga
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引用次数: 3

Abstract

Background People living with sickle cell face a lot of stigma and discrimination in Uganda. This stigma is as a result of the lack of the general conceptualization of this condition. For students, the stigma is often due to their differences like jaundice, delayed sexual maturation, and physical growth. This makes individuals with SCD targets for teasing and bullying. This study assessed the knowledge and perception among secondary school students in a rural district of Butambala at nine selected schools. The study also evaluated the use of sickle cell clubs as a tool for behavior change towards the associated stigma and discrimination. Methods A school-based cross-sectional study design was used to assess knowledge and perception towards sickle cell disease in secondary schools in Butambala district using self-administered questionnaires prior to and after set up of the sickle cell clubs. Results Out of the 375 student participants (59.5% female, 40.5% male) the majority (87.5%) were below 18 years; 68% of the respondents did not know that sickle cell is a genetic condition; 87.5% of the respondents highlighted that it is important for people with SCD to attend school; 54.4% of the respondents reported that people with SCD should not be given equal rights, while 56.0% of the respondents noted that people with SCD should not socialize. Conclusion It is evident the there is a big gap in sickle cell awareness among secondary school students coupled with a high level of stigma and discrimination. Sickle cell clubs have a positive effect towards behavior change while providing SCD knowledge and information.
加入还是不加入?乌干达布坦巴拉地区中学镰状细胞俱乐部、耻辱和歧视案例
在乌干达,镰状细胞病患者面临着许多耻辱和歧视。这种耻辱是由于缺乏对这种情况的一般概念化。对于学生来说,这种耻辱通常是由于他们的差异,如黄疸、性成熟延迟和身体发育。这使得患有SCD的人成为戏弄和欺凌的目标。本研究评估了布坦巴拉农村地区九所选定学校中学生的知识和认知。该研究还评估了镰状细胞俱乐部作为改变相关污名和歧视行为的工具的使用情况。方法采用以学校为基础的横断面研究设计,采用镰状细胞俱乐部成立前后自填问卷的方式,对Butambala地区中学镰状细胞病的知识和认知进行评估。结果在375名学生参与者中(女性59.5%,男性40.5%),大多数(87.5%)年龄在18岁以下;68%的受访者不知道镰状细胞是一种遗传性疾病;87.5%的受访者强调学童上学是重要的;54.4%的受访者认为SCD患者不应该被赋予平等的权利,56.0%的受访者认为SCD患者不应该社交。结论中学生对镰状细胞病的认知存在较大差距,对镰状细胞病的污名化和歧视程度较高。镰状细胞俱乐部在提供SCD知识和信息的同时,对行为改变有积极的影响。
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来源期刊
自引率
0.00%
发文量
13
审稿时长
16 weeks
期刊介绍: Adolescent Health, Medicine and Therapeutics is an international, peer reviewed, open access journal focusing on health, pathology, and treatment issues specific to the adolescent age group, including health issues affecting young people with cancer. Original research, reports, editorials, reviews, commentaries and adolescent-focused clinical trial design are welcomed. All aspects of health maintenance, preventative measures, disease treatment interventions, studies investigating the poor outcomes for some treatments in this group of patients, and the challenges when transitioning from adolescent to adult care are addressed within the journal. Practitioners from all disciplines are invited to submit their work as well as health care researchers and patient support groups. Areas covered include: Physical and mental development in the adolescent period, Behavioral issues, Pathologies and treatment interventions specific to this age group, Prevalence and incidence studies, Diet and nutrition, Specific drug handling, efficacy, and safety issues, Drug development programs, Outcome studies, patient satisfaction, compliance, and adherence, Patient and health education programs and studies.
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