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临床试验/NCT03747640
NCT03747640已完成不适用

Self Transcranial Direct Current Stimulation and Mindfulness-based Meditation for Pain in Older Adults With Knee Osteoarthritis (Self tDCS and Meditation for Knee Pain)

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年11月28日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Change in Clinical Pain as Assessed by a Numeric Rating Scale for Pain (NRS)

研究概览

简要总结

The purpose of this study is to determine the feasibility and preliminary efficacy of a two-week self tDCS and mindfulness-based meditation for pain in older adults with knee osteoarthritis (OA).

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • self-reported unilateral or bilateral knee OA pain, according to American College of Rheumatology criteria. According to American College of Rheumatology criteria, participants should meet at least 3 of 6 criteria, including age > 50 years, stiffness < 30 minutes, crepitus, bony tenderness, bony enlargement, and no palpable warmth.
  • have had knee OA pain in the past 3 months with an average of at least 30 on a 100 Numeric Rating Scale (NRS) for pain
  • can speak and read English
  • have a device with internet access that can be used for secure video conferencing for real-time remote supervision
  • have no plan to change medication regimens for pain throughout the trial
  • are able to travel to the coordinating center
  • are willing and able to provide written informed consent prior to enrollment

排除标准

  • Participants will be excluded if they have concurrent medical conditions that hinder the completion of the protocol, including any of the following
  • history of brain surgery, brain tumor, seizure, stroke, or intracranial metal implantation
  • serious medical illness, such as uncontrolled hypertension (i.e., systolic blood pressure/ diastolic blood pressure ≥ 150/95 mm Hg), heart failure, or history of acute myocardial infarction
  • alcohol/substance abuse
  • cognitive impairment
  • pregnancy or lactation
  • hospitalization within the preceding year for psychiatric illness

结局指标

主要结局

Change in Clinical Pain as Assessed by a Numeric Rating Scale for Pain (NRS)

时间窗: baseline, 2 weeks

The NRS assess average pain over the past 24 hours from 0 (no pain) to 100 (most intense pain imaginable).

次要结局

  • Psychosocial Symptoms as Assessed by PROMIS Sleep Disturbance-short Form(2 weeks)
  • Psychosocial Symptoms as Assessed by PROMIS Depression-short Form(2 weeks)
  • Psychosocial Symptoms as Assessed by the Pain Catastrophizing Scale (PCS)(2 weeks)
  • Number of Participants Who Were Assessed by Functional Near-infrared Spectroscopy (fNIRS)(baseline)
  • Change in Clinical Pain as Assessed by the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)(baseline, 2 weeks)
  • Psychosocial Symptoms as Assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety-short Form(baseline)
  • Psychosocial Symptoms as Assessed by the PROMIS Anxiety-short Form(2 weeks)
  • Number of Participants Who Were Assessed by Functional Near-infrared Spectroscopy(2 weeks)
  • Change in Experimental Pain Sensitivity as Assessed by Pressure Pain Threshold, Medial Knee(baseline, 2 weeks)
  • Change in Experimental Pain Sensitivity as Assessed by Pressure Pain Threshold, Lateral Knee(baseline, 2 weeks)
  • Psychosocial Symptoms as Assessed by the Freiburg Mindfulness Inventory (FMI)(2 weeks)
  • Change in Experimental Pain Sensitivity as Assessed by Conditioned Pain Modulation(baseline, 2 weeks)
  • Change in Experimental Pain Sensitivity as Assessed by Cold Pain Intensity(baseline, 2 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hyochol Ahn

Associate Professor & Theodore J. and Mary E. Trumble Professor

The University of Texas Health Science Center, Houston

研究点 (2)

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