Optimizing Accelerated TMS for Chronic Pain With Thompson Sampling
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Change in pain intensity
研究概览
简要总结
The purpose of this study is to evaluate the safety and efficacy of accelerated intermittent theta burst stimulation (aiTBS) targeting personalized nodes within the somato-cognitive action network (SCAN) and action motor network (AMN) for the treatment of chronic pain. The study will employ Thompson Sampling, a Bayesian reinforcement learning algorithm, to optimize stimulation site selection based on individual response patterns. This approach has the potential to revolutionize pain management by improving treatment accessibility through shortened timelines, addressing individual variations in pain networks through precision targeting, and potentially achieving more robust pain relief through accelerated neuroplasticity.
The specific aims of the study are:
- To establish the relationship between SCAN and AMN connectivity and cognitive- affective pain symptoms.
- To evaluate the efficacy of Thompson Sampling-optimized aiTBS across SCAN and AMN on affective and sensorimotor pain dimensions.
- To identify fMRI connectivity biomarkers predictive of treatment response and remission.
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
- •Ages 18 years or older
- •Ability to provide written informed consent
- •Ability to read and to communicate verbally and in writing in English
- •Chronic pain persisting for at least 12 months
- •Pain refractory to oral pain medication (defined as failing at least two different medication classes)
- •Average pain intensity of ≥5 on the Numerical Rating Scale (NRS) over the past two weeks
- •Stable pain medication regimen for at least 4 weeks prior to enrollment
- •Willing and able to attend all study visits and comply with study procedures
排除标准
- •Current substance use disorder (except for nicotine or cannabis) as determined by DSM-5 criteria
- •Active suicidal ideation with intent or plan as determined by the Columbia-Suicide Severity Rating Scale (C-SSRS)
- •Lifetime history of bipolar disorder, schizophrenia, or other psychotic disorder as determined by medical history
- •Self-reported unstable medical conditions that would pose increased risks for TMS or MRI
- •Pregnancy (as determined by urine pregnancy test) or planned pregnancy during the study period
- •Contraindications to TMS, including:
- •History of seizure or epilepsy
- •Metallic implants in the head (excluding dental fillings)
- •Cardiac pacemaker or other implanted medical devices
- •History of significant head trauma
- •History of intracranial surgery
- •Medication that significantly lowers seizure threshold that cannot be safely held
- •Contraindications to MRI, including:
- •Claustrophobia
- •Metallic implants or devices
- •Inability to lie flat for the duration of the scan
- •Current use of high-dose opioids (>90 morphine milligram equivalents daily)
- •Participation in another clinical trial of an investigational medication or device within 30 days prior to enrollment
- •Any condition that, in the investigator's opinion, would make it unsafe or difficult for the participant to complete the study
研究组 & 干预措施
Study group
Individuals with chronic pain
干预措施: MagVenture X100 Pro transcranial magnetic stimulation system (Device)
结局指标
主要结局
Change in pain intensity
时间窗: 3 months
measured by the Numerical Rating Scale (NRS) from baseline to after completion of the trial (approximately 3 months). For the NRS, the scores range from 0 to 10, where 0 indicates no pain (better outcome) and 10 is the worst pain that the participant can imagine (worse outcome)
次要结局
- Change in sleep quality score(Week 21)
- Change in pain intensity(Week 27)
- Change in sleep time(Week 21)
- Adherence to the protocol and the tolerability of the study visits/procedures(Week 27)
- Pain Catastrophizing Scale Score(Week 21)
- PROMIS Emotional Distress Score(Week 21)
- Pain vigilance and awareness questionnaire (PVAQ)(Week 21)
- Pain interference score on the Brief Pain Inventory (BPI)(Week 21)
- Connectivity between SCAN and AMN connectivity on fMRI(Day 0)
- Changes in SCAN and AMN connectivity on fMRI(Week 21)
- Pain Catastrophizing Scale Score(Day 0)
- Pain Catastrophizing Scale Score(Week 15)
- PROMIS Emotional Distress Score(Day 0)
- PROMIS Emotional Distress Score(Week 15)
- Pain vigilance and awareness questionnaire (PVAQ)(Day 0)
- Pain vigilance and awareness questionnaire (PVAQ)(Week 15)
- Pain interference score on the Brief Pain Inventory (BPI)(Day 0)
- Pain interference score on the Brief Pain Inventory (BPI)(Week 15)