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临床试验/NCT03728751
NCT03728751已完成不适用

Optimal Time for In-situ Dry Needling to Affect the Autonomic Nervous System: A Pilot Study

Florida Gulf Coast University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2018年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
Pupil diameter

研究概览

简要总结

Assessing for optimal time dry needles need to remain inside the body to have positive effect on the nervous system

详细描述

The purpose of this study is to determine what most optimal dry needling duration effect on the autonomic nervous system.

Design: The researchers will conduct a pilot study to assess the effect of dry needling on the autonomic nervous system

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18-65 years old
  • No pain at all anywhere in the body at the time of testing.
  • No caffeine containing products 3 hours before measurement and no use of over the counter Non-Steroidal Anti-Inflammatory Drug (NSAID) before the testing.

排除标准

  • Red flags identified during the subjects intake. If needling is contraindicated the subjects will be removed from the study and if necessary will be referred to an appropriate health care provider.
  • Use of blood thinners
  • History of surgery and or injury within the past six weeks
  • Evidence of central nervous system involvement, to include hyperreflexia, sensory disturbances in the hand, intrinsic muscle wasting of the hands, unsteadiness during walking, nystagmus, loss of visual acuity, impaired sensation of the face, altered taste, the presence of pathological reflexes (i.e. positive Hoffman's and/or Babinski reflexes), etc.
  • Prior surgery to the neck or thoracic spine
  • Chiropractic, Physical Therapy, Dry needling or Acupuncture treatment for their neck pain in the last 3-months
  • Inability to follow directions and keep the eye open during the measurement phase of this study

研究组 & 干预措施

study group

Experimental

Study group receiving dry needling and pupil diameter will be studied up to 23 minutes after needle placement.

干预措施: Dry needling (Procedure)

结局指标

主要结局

Pupil diameter

时间窗: 1.) 1 minute measure will be taken after accommodation of 2 minutes to the dark environment, 2.) needle placement and an immediate 1 minute second measure, 3.) every 2 minutes a measure of 1 minute to 8 post needle measures (24 minutes) total

Change in pupil diameter measured with automated pupillometry device from Micromedical.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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