{"title":"Survey on Patient and Physician Attitudes about Parkinson Clinical Trials","authors":"","doi":"10.1016/j.nurx.2006.05.033","DOIUrl":null,"url":null,"abstract":"<div><p>In March 2005, Harris Interactive® completed a study examining physicians’ and patients’ attitudes towards Parkinson’s disease clinical trials. The study was commissioned on behalf of <em>PDtrials*</em> by the Michael J. Fox Foundation for Parkinson’s Research.</p><p>Five hundred physicians (250 primary care physicians/gerontologists and 250 neurologists) and 518 people with Parkinson’s participated in the study. Nearly 80% of patients surveyed stated that they would be somewhat, very, or extremely likely to participate in a clinical trial if one were available in their area. However, seven in ten are not at all or not very aware of clinical trials and only 11% reported that their doctor ever suggested that they participate in a trial.</p><p>The survey also found that, among physicians who treat people with Parkinson’s, 96% agree that clinical trials are necessary to find better treatments for the disease. However, the majority have discussed clinical trials with just 10% or less of their patients and never referred a patient to a clinical trial.</p><p>Only 14% of primary care physicians, 21% of neurologists, and 18% of patients surveyed indicated that they are somewhat or very satisfied with the amount of information available about clinical trials for Parkinson’s disease.</p><p>The Harris Interactive study confirms the assumption that there is a clinical trials information gap and the critical role of <em>PDtrials</em>, a national initiative dedicated to increasing education and awareness about clinical research by providing information to help people with Parkinson’s learn and make informed decisions about participating in clinical trials.</p><p>*<em>PDtrials</em> is led by the Parkinson’s Disease Foundation in collaboration with the American Parkinson Disease Association, The Michael J. Fox Foundation for Parkinson’s Research, the National Parkinson Foundation, the Parkinson’s Action Network, The Parkinson Alliance and WE MOVE. The campaign is advised by the National Institute of Neurological Disorders and Stroke (NIH), the Parkinson Study Group, the Parkinson Pipeline Project and the Parkinson’s Institute.</p></div>","PeriodicalId":87195,"journal":{"name":"NeuroRx : the journal of the American Society for Experimental NeuroTherapeutics","volume":"3 3","pages":"Page 415"},"PeriodicalIF":0.0000,"publicationDate":"2006-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.nurx.2006.05.033","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NeuroRx : the journal of the American Society for Experimental NeuroTherapeutics","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1545534306001039","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In March 2005, Harris Interactive® completed a study examining physicians’ and patients’ attitudes towards Parkinson’s disease clinical trials. The study was commissioned on behalf of PDtrials* by the Michael J. Fox Foundation for Parkinson’s Research.
Five hundred physicians (250 primary care physicians/gerontologists and 250 neurologists) and 518 people with Parkinson’s participated in the study. Nearly 80% of patients surveyed stated that they would be somewhat, very, or extremely likely to participate in a clinical trial if one were available in their area. However, seven in ten are not at all or not very aware of clinical trials and only 11% reported that their doctor ever suggested that they participate in a trial.
The survey also found that, among physicians who treat people with Parkinson’s, 96% agree that clinical trials are necessary to find better treatments for the disease. However, the majority have discussed clinical trials with just 10% or less of their patients and never referred a patient to a clinical trial.
Only 14% of primary care physicians, 21% of neurologists, and 18% of patients surveyed indicated that they are somewhat or very satisfied with the amount of information available about clinical trials for Parkinson’s disease.
The Harris Interactive study confirms the assumption that there is a clinical trials information gap and the critical role of PDtrials, a national initiative dedicated to increasing education and awareness about clinical research by providing information to help people with Parkinson’s learn and make informed decisions about participating in clinical trials.
*PDtrials is led by the Parkinson’s Disease Foundation in collaboration with the American Parkinson Disease Association, The Michael J. Fox Foundation for Parkinson’s Research, the National Parkinson Foundation, the Parkinson’s Action Network, The Parkinson Alliance and WE MOVE. The campaign is advised by the National Institute of Neurological Disorders and Stroke (NIH), the Parkinson Study Group, the Parkinson Pipeline Project and the Parkinson’s Institute.
2005年3月,Harris Interactive®完成了一项研究,调查医生和患者对帕金森病临床试验的态度。这项研究是由迈克尔·j·福克斯帕金森氏症研究基金会委托pd试验*进行的。500名医生(250名初级保健医生/老年学家和250名神经学家)和518名帕金森患者参与了这项研究。近80%接受调查的患者表示,如果他们所在地区有临床试验,他们会多少、非常或极有可能参加临床试验。然而,十分之七的人根本不知道或不太了解临床试验,只有11%的人报告说他们的医生曾建议他们参加临床试验。调查还发现,在治疗帕金森氏症患者的医生中,96%的人认为有必要进行临床试验,以找到更好的治疗方法。然而,大多数医生只与10%或更少的患者讨论过临床试验,从未将患者转介到临床试验。只有14%的初级保健医生、21%的神经科医生和18%的受访患者表示,他们对帕金森氏症临床试验的现有信息量有些满意或非常满意。哈里斯互动研究证实了临床试验信息差距和PDtrials的关键作用的假设,PDtrials是一项国家倡议,致力于通过提供信息来帮助帕金森患者学习和做出参与临床试验的明智决定,从而提高对临床研究的教育和认识。*PDtrials由帕金森病基金会牵头,与美国帕金森病协会、Michael J. Fox帕金森病研究基金会、国家帕金森基金会、帕金森病行动网络、帕金森联盟和WE MOVE合作。该运动由国家神经疾病和中风研究所(NIH)、帕金森研究小组、帕金森管道项目和帕金森研究所提供建议。