Moore Heidi K, Wohlreich Madelaine M, Wilson Michael G, Mundt James C, Fava Maurizio, Mallinckrodt Craig H, Greist John H
Healthcare Technology Systems, Inc., Madison, Wisconsin, USA.
Psychiatry (Edgmont). 2007 Mar;4(3):30-8.
Most clinical trials measure patient responses weekly, requiring patients to accurately recall and report their symptoms from the previous six days. More frequent assessments would be less susceptible to recall errors and recency effects as weekly assessments, but increased office visits burden clinicians and patients and can lead to higher attrition or non compliance. Interactive voice response (IVR) technology permits data collection at greater frequencies with minimal reporting burdens. An ancillary study within a randomized clinical trial evaluated the use of IVR to gather measures of patients' ratings of emotional and painful symptoms of depression on a daily basis. Unmedicated patients randomized to a starting dose of duloxetine of 30 mg QD (n=67) or 60 mg QD (n=70) called an IVR system daily to complete Verbal Numeric Scales for pain and Patient Global Impression of Improvement for both physical and emotional changes. Patients' compliance with daily IVR assessments was examined, and the IVR data obtained showed that patients started at 60 mg reported less pain and greater physical and emotional improvements than patients started at 30 mg. Dose related differences were evident as early as one day after the start treatment. This study provides new data about the usefulness of daily IVR assessments in clinical research and supports other studies regarding early symptom improvement with duloxetine.
大多数临床试验每周测量患者的反应,这就要求患者准确回忆并报告前六天的症状。与每周评估相比,更频繁的评估不易受到回忆误差和近因效应的影响,但增加门诊就诊次数会给临床医生和患者带来负担,并可能导致更高的失访率或不依从性。交互式语音应答(IVR)技术允许以更高的频率收集数据,同时报告负担最小。一项随机临床试验中的辅助研究评估了使用IVR每天收集患者对抑郁症情绪和疼痛症状评分的情况。随机接受度洛西汀起始剂量为每日30毫克(n = 67)或每日60毫克(n = 70)的未用药患者每天拨打IVR系统,以完成疼痛的言语数字量表以及身体和情绪变化的患者总体改善印象。检查了患者对每日IVR评估的依从性,获得的IVR数据显示,起始剂量为60毫克的患者比起始剂量为30毫克的患者报告的疼痛更少,身体和情绪改善更大。剂量相关差异在开始治疗后一天就很明显。这项研究提供了关于每日IVR评估在临床研究中的有用性的新数据,并支持了其他关于度洛西汀早期症状改善的研究。