ACTRN12620000414910已完成未知
Effect of electroencephalography based infraslow neurofeedback on pain and function in individuals with chronic low back pain: A pilot double-blind randomised controlled study.
Dr Divya Adhia0 个研究点目标入组 60 人开始时间: 2020年3月27日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 75 Years(—)
- 性别
- All
入选标准
- •Participants with a diagnosis of CLBP will be eligible to participate. To be included in the study, participants must meet all of the following inclusion criteria:
- •Capable of understanding and signing an informed consent form
- •Age between 18 to 75 years on the day of the consent
- •Pain in the lower back area (region between the 12th rib and the gluteal fold) that occurs every day for more than or equal to 3 months
- •A score of more than or equal to 4 on the 11-point numeric pain rating scale (NPRS, 0 is No pain to 10 is Worst pain) in the past 4 weeks
- •A disability score of more than or equal to 5 on Roland–Morris Disability Questionnaire
排除标准
- •Inflammatory arthritis
- •Undergoing any therapy from a health professional (e.g. physiotherapists or chiropractor)
- •Recent soft tissue injuries of the back in the last 3 months
- •History of surgery to the back region
- •Radicular pain and radiculopathy
- •History of neurological diseases
- •Unstable medical or psychiatric conditions
- •History of epilepsy or seizures
- •Presence of any peripheral neuropathy or vascular pathology
- •Sleep Apnoe
- •Hearing problems (hearing loss or tinnitus)
- •Alcohol or substance abuse
- •Dyslipidaemia
- •Cognitive impairments (dementia, post-traumatic stress disorders, Alzheimer’s disease): A total score of 24 or below on Mini-Mental State Examination
- •History of uncontrolled/untreated hypertension
- •Presence of any pacemaker or defibrillator
- •Presence of any electronic implants or metal implant in the body (particularly head and neck)
- •Recent or current pregnancy
- •Participants who, in the opinion of the investigators, do not understand the information and procedures of the study, or would not be compliant with them.
- •Participants with current intake of any centrally acting medications (e.g. antidepressants, anticonvulsants, neuropathic pain drugs) or intention of taking new medications in the next 3 months.
研究者
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