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Patients' perspectives on participation in clinical trials and subsequent ethical challenges in a hospital setting in Jordan

机译:患者对约旦医院环境中临床试验及随后伦理挑战的观点

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Background The number of global clinical trials is increasing. Recruitment rate in clinical trials is a challenging task that affects sample size, power of the study, and adequate representation of the targeted population. An understanding of the worries and reasons why patients may refrain from participation in trials may lead to improved enrollment rates. Objectives To assess the rate of patients who are willing to participate in clinical trials, and aspects that might have an impact on the patients' willingness to participate. Setting Government tertiary hospital in Jordan. Methods This is a cross-sectional study. Patients were interviewed by pharmacists in different clinics in a tertiary hospital and information was collected using a data collection sheet. Main outcome measure Factors that might predict the inclination of a patient to participate in clinical trials, and the rate of willingness to participation in randomized controlled trials in cancer patients compared to non-cancer patients. Results A total of 1193 participants were enrolled in the study, one hundred and thirty-five participants (11.3%) had cancer and 80% of the participants had at least one chronic medical condition. Majority of patients (n = 882, 73.9%) believed that trials were safe and 1106 (92.7%) patients thought they were important. Age, education level, income, having cancer or any chronic medical condition, and degree of control of chronic diseases were statistically significant predictors of the willingness of patients to participate in trials. Patients with cancer had a higher rate of acceptance to participation in randomized controlled trials compared to non-cancer patients, 80.0% versus 62.4%, p value < 0.001. Conclusion In general, almost two-thirds of patients were willing to participate in clinical trials, with a higher rate in cancer patients. Factors such as education level, income, and extent of control of medical conditions that might refrain patients from enrollment in trials will lower recruitment rate and must be addressed and taken into consideration before launching clinical trials.
机译:背景技术全球临床试验的数量正在增加。临床试验中的招聘率是一个具有挑战性的任务,影响研究的样本大小,研究权力,适当的目标人口的代表性。了解患者可能避免参与审判的担忧和原因可能会导致入学率提高。目的评估愿意参与临床试验的患者的速度以及可能对患者参与的愿意产生影响的方面。在约旦设防政府高等教育医院。方法这是一个横断面研究。患者在教学家在第三节医院中的不同诊所进行采访,并使用数据收集表收集信息。主要结果测量可能预测患者参与临床试验的倾向,以及与非癌症患者相比,参与癌症患者随机对照试验的意愿速度。结果共有1193名参与者参加了这项研究,一百三十五名参与者(11.3%)患有癌症,80%的参与者至少有一种慢性医疗病症。大多数患者(n = 882,73.9%)认为,试验是安全的,1106名(92.7%)患者认为它们很重要。年龄,教育水平,收入,患有癌症或任何慢性医疗状况以及慢性病的控制程度是患者参与试验的统计学意义的预测因子。与非癌症患者相比,癌症患者对随机对照试验的接受程度较高,80.0%对62.4%,P值<0.001。结论一般来说,近三分之二的患者愿意参与临床试验,癌症患者的速度较高。教育水平,收入和控制患者的教育水平,收入和程度等因素,这些因素可以避免患者入学患者的患者将降低招聘率,并且必须在发动临床试验之前进行审议并考虑。

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