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临床试验/ACTRN12620000414910
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

发起方
Dr Divya Adhia

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