NCT06442527撤回不适用
Using Virtual Reality Before Transcranial Magnetic Stimulation for the Treatment of OCD
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 入组人数
- 5
- 试验地点
- 2
- 主要终点
- Tolerability of VR treatment by qualitative assessment
研究概览
简要总结
This study will focus on the use of Virtual Reality (VR) technology in patients receiving treatment using Transcranial Magnetic Stimulation (TMS) for Obsessive-Compulsive Disorder (OCD)
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Participants must be at least 18 years old
- •Patients must have been clinically evaluated by a Yale Interventional Psychiatry Service physician who has deemed them appropriate to receive TMS for the treatment of OCD
- •Ability and willingness, in the investigator's judgement, to comply with the study procedure and study requirements.
排除标准
- •Hearing or visual impairment to the degree that would interfere with ability to see or hear VR content.
- •Difficulty in understanding spoken or written English
- •Pregnancy
- •History of seizure disorder
- •Unable to provide informed consent
- •Dementia or other cognitive disorder or intellectual disability that would impair the subject's ability to understand the study procedure (per investigator judgment)
- •Any implanted medical device, risk of interference with which by the VR device in the investigator's judgment can put patient at additional undue risk.
- •Any other medical or psychiatric comorbidity that the investigator judges would put the participant at additional undue risk due to study participation or would impair subject's ability to participate in the study.
- •Was previously enrolled/randomized into the study
研究组 & 干预措施
Treatment Group
Experimental
This single arm will include all participants of the study, who will all receive the intervention
干预措施: Virtual Reality (Device)
结局指标
主要结局
Tolerability of VR treatment by qualitative assessment
时间窗: Within 1 hour after each treatment session
Tolerability will be assessed by open-ended interview of the patient about their experience and any difficulty tolerating VR
次要结局
未报告次要终点
研究者
研究点 (2)
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