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Completed

NCT Number: NCT03728751

Optimal Time for In-situ Dry Needling to Affect the Autonomic Nervous System

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

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Integrated Therapy Practice PC

Hobart, Indiana, 46342, United States

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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

Treatment and study plan

dry needling

Procedure

Paravertebral dry needling C7-T4. Total of 8 needles.

Primary outcomes

  1. Pupil diameter

    Time frame: 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.

Sponsors and collaborators

Lead sponsor

Florida Gulf Coast University

Other

Registry information

Official study title

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

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Nov 2, 2018
Registry last updated
Nov 2, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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