Rahman Mahbubur, Morita Satoshi, Fukui Tsuguya, Sakamoto Junichi
Clinical Practice Evaluation and Research Center, St. Luke's Life Science Institute, Tokyo 104-8560, Japan.
J Epidemiol. 2005 Mar;15(2):38-40. doi: 10.2188/jea.15.38.
Physicians' perception and attitudes towards a research topic and trial management could influence their participation in a randomized controlled trial. The objectives of this study were to determine the reasons for physicians' participation in and attitudes towards the Candesartan Antihypertensive Survival Evaluation in Japan (CASE-J) trial.
CASE-J's main objective is to compare the effectiveness of an angiotensin II receptor antagonist (candesartan cilexetil) with that of a calcium channel blocker (amlodipine besilate) in terms of the incidence of cardiovascular events among high-risk hypertensive patients. We conducted a questionnaire survey among the physicians (n = 512) participating in that trial to determine the reasons behind their participation and to elicit their reactions to the trial management.
Eighty-eight percent of the 512 participating physicians responded to our survey. The main reasons for participation were clear objectives of the trial (85.1%), a simple protocol (61.1%), interest in finding out the inhibiting effects of the drugs on cardiac events (80.2%), and a well-organized support system (59.8%). As for negative factors, case registration and follow-up were considered cumbersome by 28.6% and 10.8%, respectively while 44.2% stated that support by the clinical research coordinators provided by the trial management authority was necessary for case screening, recruitment process, patient registration, and follow-up. Multivariate logistic regression analysis showed that participants who did not use a computer very regularly (odds ratio = 1.9, 95% confidence interval = 1.1-3.6) were more likely to consider the case registration and follow-up procedures as a cumbersome.
The information generated by this study could be useful in designing future randomized controlled trials in Japan and abroad.
医生对研究主题和试验管理的认知与态度可能会影响他们参与随机对照试验。本研究的目的是确定医生参与日本坎地沙坦抗高血压生存评估试验(CASE-J)的原因及态度。
CASE-J的主要目标是比较血管紧张素II受体拮抗剂(坎地沙坦酯)与钙通道阻滞剂(苯磺酸氨氯地平)在高危高血压患者心血管事件发生率方面的有效性。我们对参与该试验的医生(n = 512)进行了问卷调查,以确定他们参与的原因,并了解他们对试验管理的反应。
512名参与医生中有88%回应了我们的调查。参与的主要原因是试验目标明确(85.1%)、方案简单(61.1%)、对了解药物对心脏事件的抑制作用感兴趣(80.2%)以及支持系统组织完善(59.8%)。至于负面因素,分别有28.6%和10.8%的医生认为病例登记和随访繁琐,而44.2%的医生表示试验管理机构提供的临床研究协调员的支持对于病例筛选、招募过程、患者登记和随访是必要的。多因素逻辑回归分析显示,不经常使用计算机的参与者(比值比 = 1.9,95%置信区间 = 1.1 - 3.6)更有可能认为病例登记和随访程序繁琐。
本研究所得信息可能有助于在日本国内外设计未来的随机对照试验。