Effectiveness and Safety of Transcranial Direct Current Stimulation for Pain Changes in Patients With Central Post-Stroke Pain
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 23
- 试验地点
- 2
- 主要终点
- Change of pain score in Brief Pain Inventory(BPI)
研究概览
简要总结
The purpose of this study is to verify the effectiveness and safety of transcranial direct current stimulation in patients with central post-stroke pain.
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
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 19 Years 至 90 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adults aged 19 to 90 years old
- •Those who have been diagnosed with first-time stroke through doctors' clinical observation and brain imaging diagnosis
- •A person whose stroke lesions are cortex or subcortex
- •A person who satisfies 'Mandatory criteria'
- •Those with cognitive ability to understand and follow the researcher's instructions
- •Those who voluntarily agree to participate in this clinical trial and signed the agreement
排除标准
- •Those who have a fracture or have undergone orthopedic surgery
- •In case of accompanying serious neurological diseases
- •In case of major psychiatric diseases such as major depression disorders, schizophrenia, bipolar disorders, and dementia
- •Those with complex part pain syndrome by Budapest Criteria
- •If there is a cause of other pain in the relevant area, such as peripheral nerve damage
- •Persons included in the exclusion of transcranial direct current stimulation
- •If the researcher is judged to be judged that the participation in this study is not appropriate
结局指标
主要结局
Change of pain score in Brief Pain Inventory(BPI)
时间窗: Baseline, after 2 weeks(after the end of intervention)
Brief Pain Inventory(BPI) is used for measurement. The Brief Pain Inventory (BPI) is a tool used to assess pain severity and its impact on daily functions. The BPI typically uses an 11-point numeric rating scale (NRS) for its pain severity and pain interference items. Each item is rated from 0 to 10. Pain Severity: 0 (no pain) to 10 (pain as bad as you can imagine). Pain Interference: 0 (does not interfere) to 10 (completely interferes).
次要结局
- Change of depression score in Beck Depression Inventory-II(BDI-II)(Baseline, after 2 weeks(after the end of intervention))
- Change of quality of life score in the EuroQol Five-dimensions-Three-Level Quality of Life Instrument(EQ-5D-3L)(Baseline, after 2 weeks(after the end of intervention))
- Change of pain score in Neuropathic Pain Scale(NPS)(Baseline, after 2 weeks(after the end of intervention))
研究者
Yong-il Shin
Professor
Pusan National University Yangsan Hospital