Women’s health concern in Jordan: knowledge, practice and barriers toward cervical cancer screening

IF 1.2 Q4 HEALTH POLICY & SERVICES International Journal of Human Rights in Healthcare Pub Date : 2021-12-01 DOI:10.1108/ijhrh-04-2021-0085
Roqia Maabreh, R. Y. Al-husban, H. Al-Akash, Noha Al-Shdayfat
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引用次数: 1

Abstract

Purpose Cervical cancer (CC) is one of the most important health issues faced by women worldwide. The purpose of this study is to identify Jordanian women’s knowledge, barriers and measures pertaining to risk factors and screening choices of CC (Pap smear tests). Design/methodology/approach This study applied a cross sectional design by collecting data from a convenient sample of 200 women between 20 and 70 years of age in health and public centers in Jordan. Data was then analyzed using the descriptive statistical tools of SPSS, version 21. Findings The findings revealed that 55.5% of the participants had no information about the Pap smear, and 75% did not know the risk factors. Moreover, 50% of the sample did not know where to take the test, and 50% reported a lack of encouragement from the husband to undertake the test. More than half of the participants (56.5%) expressed fear that cervical screening would be a painful examination even though they reported not having any previous experience with the test. Originality/value Based on these findings, public education about CC screening is essential, including advertising and a campaign similar to the breast cancer awareness programs in Jordan, as a way of encouraging early screening to improve the health of women.
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约旦妇女的健康问题:癌症筛查的知识、实践和障碍
目的癌症(CC)是全球妇女面临的最重要的健康问题之一。本研究的目的是确定约旦妇女在CC(巴氏涂片检查)的风险因素和筛查选择方面的知识、障碍和措施。设计/方法/方法本研究采用横断面设计,从200名20至70岁的妇女中收集数据 约旦卫生和公共中心的年龄。然后使用SPSS版本21的描述性统计工具对数据进行分析。结果显示,55.5%的参与者没有巴氏涂片的信息,75%的参与者不知道风险因素。此外,50%的样本不知道在哪里进行测试,50%的人表示丈夫没有鼓励他们进行测试。超过一半的参与者(56.5%)表示担心宫颈筛查会是一项痛苦的检查,尽管他们报告说以前没有任何检查经验。创意/价值基于这些发现,关于CC筛查的公共教育至关重要,包括广告和类似于约旦癌症乳腺癌宣传计划的活动,作为鼓励早期筛查以改善妇女健康的一种方式。
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来源期刊
CiteScore
2.90
自引率
7.10%
发文量
48
期刊介绍: nternational Journal of Human Rights in Healthcare (IJHRH) is an international, peer reviewed journal with a unique practical approach to promoting race equality, inclusion and human rights in health and social care. The journal publishes scholarly and double blind peer-reviewed papers of the highest standard, including case studies and book reviews. IJHRH aims include: -To explore what is currently known about discrimination and disadvantage with a particular focus on health and social care -Push the barriers of the human rights discourse by identifying new avenues for healthcare practice and policy internationally -Create bridges between policymakers, practitioners and researchers -Identify and understand the social determinants of health equity and practical interventions to overcome barriers at national and international levels. The journal welcomes papers which use varied approaches, including discussion of theory, comparative studies, systematic evaluation of interventions, analysis of qualitative data and study of health and social care institutions and the political process. Papers published in IJHRH: -Clearly demonstrate the implications of the research -Provide evidence-rich information -Provoke reflection and support critical analysis of both challenges and strengths -Share examples of best practice and ‘what works’, including user perspectives IJHRH is a hugely valuable source of information for researchers, academics, students, practitioners, managers, policy-makers, commissioning bodies, social workers, psychologists, nurses, voluntary sector workers, service users and carers internationally.
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