A Pilot Study to Evaluate the Safety and Efficacy of the Karuna Virtual Reality Program for the Treatment of Chronic Low Back Pain
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 2
- 主要终点
- Physical Functioning measured by PROMIS 6 (Patient Reported Outcome Measurement Information System)
研究概览
简要总结
Chronic low back pain is highly prevalent in US adults and is a major cause of missed work days and disability. While several treatment options exist, chronic opioids are commonly used for these conditions even though there are limited data supporting efficacy, and clear evidence of harm associated with chronic opioid administration.
Virtual reality has been proposed as a treatment option that may lead to decreased pain and improved physical functioning, while avoiding the harms associated with medication management. This study is intended to obtain preliminary safety and efficacy data to guide the design of a larger clinical trial.
详细描述
This is a pilot study to evaluate the safety and efficacy of the Kauruna Virtual Reality program for the treatment of chronic low back pain. This study is intended to document the safety and efficacy of the use of virtual reality for the treatment of chronic low back pain. The primary outcome measure will be physical functioning as measured by the PROMIS 6. Secondary outcome measures include patient-reported pain intensity, adverse side effects, disability as measured by the Oswestry Low back disability questionnaire, and mental functioning as assessed using the PHQ-9 and GAD-7. Finally, impact on opioid use in patients on chronic opioids will be assessed by documentation of daily opioid dose in oral morphine equivalents.
Forty adult patients with chronic low back pain who are receiving care through the Penn Pain Medicine Center are eligible to participate in the study. The study will consist of a screening visit, followed by randomization into 1 of 2 study groups. Both study groups will participate in two 20-minute virtual reality sessions a week for 8 weeks. Study group 1 will participate in 20 minutes of mindfulness mediation. Study Group 2 will undergo initial sessions focused on graded motor imagery, followed by sessions focused on graded exposure. Patient-reported outcomes data will be obtained at baseline, then weekly during the 8-week study period, then 4 weeks following completion of the study sessions.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Participant)
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
- •Age over 18
- •Able to speak and read English
- •A history of chronic low back pain for at least 6 months
- •No changes to medications within 30 days of randomization
- •Able to provide outcomes data through the electronic patient-reported outcome data collection system
排除标准
- •Age less than 18 years.
- •Pregnant women
- •Cognitive impairment that limits ability to participate in the study, including the provision of outcome data through the electronic patient-reported outcome data collection system.
- •Unable to stand for at least 15 minutes
- •Employees or students of the University of Pennsylvania
结局指标
主要结局
Physical Functioning measured by PROMIS 6 (Patient Reported Outcome Measurement Information System)
时间窗: 12 weeks
Physical functioning reported on a scale 1 (unable to do) to 5 (without any difficulty)
次要结局
- Mental Functioning measured by GAD-7 (Generalized Anxiety Disorder)(12 weeks)
- Disability measured by the Oswestry Low Back Disability Questionnaire(12 weeks)
- Patient-Reported Pain Intensity(12 weeks)
- Mental Functioning measured by PHQ-9 (Patient Health Questionnaire)(12 weeks)
- Adverse Events(12 weeks)
研究者
Michael Ashburn, MD, MPH
Director of Pain Medicine and Palliative Care
University of Pennsylvania