交互式CBT治疗头痛和放松训练(iCHART):交互式语音应答技术对退伍军人创伤后头痛认知行为治疗的单臂试验研究方案

Q3 Medicine
Amy S Grinberg, Olivia Datre, Daniel G. Rogers, S. W. Clark, S. Takagishi, J. Ney, E. Seng, B. Fenton, J. Sico
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引用次数: 0

摘要

创伤后头痛(PTH)是一种持续性且高度致残的疾病。头痛的认知行为疗法(CBT-HA)降低了头痛的频率和严重程度,提高了人们的生活质量,但它没有得到充分利用,许多人无法获得。利用技术为头痛提供循证心理治疗可能会解决治疗参与的障碍。这项单臂、单点试点试验旨在测试通过交互式语音响应技术(IVR)进行的五次CBT-HA干预的可行性、可接受性、临床信号和成本。参与者将包括35名PTH退伍军人,他们在弗吉尼亚州康涅狄格州医疗保健系统内接受护理。参与者将在基线磨合期内完成一次入学面试和一份9项、30天的电子头痛日记。治疗结束后,参与者将立即再次进行同样的日记。基线评估期结束后,符合条件的参与者将通过IVR接受为期10周的CBT-HA,包括对患者报告的结果进行自动每日评估,并从研究治疗师处检索每两周一次的定制反馈。此外,参与者将访问电子患者工作簿,研究治疗师将通过安全的提供者仪表板可视化患者报告的数据。参与者将在基线、治疗后立即完成(第10周)和治疗后1个月完成(第14周)时完成经验证和可靠的评估措施。主要临床信号结果是自报告头痛天数的变化,从治疗前的30天基线磨合期(第−4至0周)到治疗后的30天(第10-14周)。配对样本t检验将探索基线结果的变化。所有成本分析都将是探索性的,并将使用微观成本计算技术。临床试验.gov:NCT05093556。注册日期:2021年10月26日。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interactive CBT for headache and relaxation training (iCHART): Study protocol of a single-arm trial of interactive voice response technology delivery of cognitive-behavioral therapy for Veterans with post-traumatic headache
Post-traumatic headache (PTH) is persistent and highly disabling. Cognitive-behavioral therapy for headache (CBT-HA) reduces headache frequency and severity and improves people’s quality of life, yet it is underutilized and inaccessible to many. Leveraging technology to deliver evidence-based psychological treatments for headache may address barriers to treatment engagement. This single-arm, single-site pilot trial aims to test the feasibility, acceptability, clinical signal, and cost of a five-session CBT-HA intervention delivered via interactive voice response technology (IVR). Participants will include 35 Veterans with PTH receiving care within VA Connecticut Healthcare System. Participants will complete an intake interview and a 9-item, 30-day electronic headache diary during a baseline run-in period. The same diary will be done again by participants immediately after treatment completion. Following the baseline assessment period, eligible participants will receive CBT-HA via IVR for 10 weeks, including an automated daily assessment of patient-reported outcomes and retrieval of biweekly tailored feedback from a study therapist. In addition, participants will access an electronic patient workbook, and study therapists will visualize patient-reported data through a secure provider dashboard. Participants will complete validated and reliable assessment measures at baseline, immediately post-treatment completion (week 10), and 1-month post-treatment completion (week 14). The primary clinical signal outcome is the change in self-reported headache days from the 30-day baseline run-in period before treatment (weeks −4 to 0) to the 30-day post-treatment completion (weeks 10–14). Paired-samples t-tests will explore changes in outcomes from baseline. All cost analyses will be exploratory and will use micro-costing techniques. Clinical Trials.gov: NCT05093556. Registered October 26, 2021.
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来源期刊
Cephalalgia Reports
Cephalalgia Reports Medicine-Neurology (clinical)
CiteScore
2.50
自引率
0.00%
发文量
17
审稿时长
9 weeks
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