King Amanda L, Acquaye Alvina A, Mendoza Tito, Reyes Jennifer, Stockdill Macy, Gilbert Mark R, Armstrong Terri S, Vera Elizabeth
National Cancer Institute, National Institutes of Health.
Res Sq. 2023 Feb 16:rs.3.rs-2521990. doi: 10.21203/rs.3.rs-2521990/v1.
Primary brain tumor (PBT) patients experience higher levels of distress and anxiety than other solid tumor patients, particularly at the time of clinical evaluation when uncertainty about disease status is high ("scanxiety"). There is promising evidence supporting use of virtual reality (VR) to target psychological symptoms in other solid tumor patients, though PBT patients have not been studied extensively in this context. The primary aim of this phase 2 clinical trial is to establish the feasibility of a remote VR-based relaxation intervention for a PBT population, with secondary aims designed to determine preliminary efficacy of improving distress and anxiety symptoms. PBT patients (N=120) with upcoming MRI scans and clinical appointments who meet eligibility will be recruited to participate in a single arm trial conducted remotely through the NIH. Following completion of baseline assessments, participants will complete a 5-minute VR intervention via telehealth using a head-mounted immersive device while under supervision of the research team. Following the intervention, over the course of 1 month patients can use VR at their discretion with follow-up assessments done immediately post-VR intervention, as well as 1 week and 4 weeks later. Additionally, a qualitative phone interview will be conducted to assess patient satisfaction with the intervention. Use of immersive VR is an innovative interventional approach to target distress and scanxiety symptoms in PBT patients who are at high risk for experiencing these symptoms leading into their clinical appointments. Findings from this study may inform design of a future multicenter randomized VR trial for PBT patients and may aid in development of similar interventions for other oncology populations. clinicaltrials.gov (NCT04301089), registered 9 March 2020.
原发性脑肿瘤(PBT)患者比其他实体瘤患者经历更高水平的痛苦和焦虑,尤其是在临床评估时,此时疾病状态的不确定性很高(“扫描焦虑”)。有证据支持使用虚拟现实(VR)来针对其他实体瘤患者的心理症状,尽管在这种情况下对PBT患者的研究并不广泛。这项2期临床试验的主要目的是确定基于远程VR的放松干预对PBT人群的可行性,次要目的是确定改善痛苦和焦虑症状的初步疗效。符合条件的即将进行MRI扫描和临床预约的PBT患者(N = 120)将被招募参加通过美国国立卫生研究院远程进行的单臂试验。在完成基线评估后,参与者将在研究团队的监督下,通过远程医疗使用头戴式沉浸式设备完成5分钟的VR干预。干预后,在1个月的时间里,患者可以自行使用VR,并在VR干预后立即、1周和4周后进行随访评估。此外,还将进行定性电话访谈,以评估患者对干预的满意度。使用沉浸式VR是一种创新的干预方法,可针对在临床预约前有高风险出现这些症状的PBT患者的痛苦和扫描焦虑症状。这项研究的结果可能为未来针对PBT患者的多中心随机VR试验的设计提供信息,并可能有助于为其他肿瘤人群开发类似的干预措施。clinicaltrials.gov(NCT04301089),于2020年3月9日注册。