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Sensor Measurement of Acupuncture Needle Manipulation - Article


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Acupuncture


Clinical Trial: Sensor Measurement of Acupuncture Needle Manipulation

This study is currently recruiting patients.

Sponsored by: National Center for Complementary and Alternative Medicine (NCCAM)
Information provided by: National Center for Complementary and Alternative Medicine (NCCAM)

Purpose

The purpose of this study is to develop and test a sensor system capable of measuring acupuncture needle manipulation and torque in a clinical setting.

Study hypothesis: Torque will be greater on the side of the back with musculoskeletal pain compared with the side without pain.

Condition Treatment or Intervention Phase
Back Pain
 Procedure: Acupuncture
Phase I

MedlinePlus related topics:  Back Pain

Study Type: Interventional
Study Design: Educational/Counseling/Training, Non-Randomized, Open Label, Uncontrolled, Parallel Assignment, Safety Study

Official Title: Acupuncture Needling Torque Sensor

Further Study Details: 
Primary Outcomes: Feasibility of use of needle torque sensor in clinical practice, education, and research
Expected Total Enrollment:  30

Study start: September 2004;  Expected completion: March 2005
Last follow-up: December 2004;  Data entry closure: March 2005

Acupuncture is an ancient Chinese practice that involves the use of specialized needles to stimulate parts of the body. The number of Americans who use acupuncture services continues to grow each year. Two elements required to deliver high-quality acupuncture treatment are identification of the appropriate acupuncture points and proper manipulation of the acupuncture needle. Despite a growing awareness of the importance of proper needle techniques, no tool capable of objectively measuring needle manipulation in a clinical setting has ever been developed. Such a tool would have applications in acupuncture research, teaching, and clinical practice. This study will develop and test a simple hand-held sensor capable of making such objective needle torque measurements.

There are two parts to this study. In Part 1, researchers will develop the hand-held sensor (called the AcuSensor) that will be mounted to the handle of an acupuncture needle and will measure torque during manual needle manipulation.

In Part 2, the sensor will be tested for accuracy and reliability in three different groups. Group 1 will consist of patients with unilateral musculoskeletal back pain. Group 1 participants will undergo one session of acupuncture treatment while torque measurement and needle manipulation techniques are examined. In Group 2, practitioners and students at two leading acupuncture schools will use the AcuSensor during their teaching clinics. Teachers and students will complete a questionnaire to evaluate the sensor's usefulness. Experienced acupuncturists comprise Group 3; they will receive AcuSensor training and evaluate the performance of the AcuSensor in clinical practice. Information about the range and variability of torque measurements produced by different practitioners and techniques will be obtained from use of the sensor. Group 3 acupuncturists will also guess needle torque before and after training with the sensor turned off in order to determine the way AcuSensor training affects acupuncturists' sensory perception of needle grasp.

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria for Group 1 Participants:


Location and Contact Information

Debbie J. Stevens-Tuttle, BA      802-656-6894    debbie.stevens-tuttle@uvm.edu

Vermont
      University of Vermont State and Agricultural College, Burlington,  Vermont,  05405,  United States; Recruiting
Helene M. Langevin, MD  802-656-1004    helene.langevin@uvm.edu 
Debbie J. Stevens-Tuttle, BA  802-656-6894    debbie.stevens-tuttle@uvm.edu 
Helene M. Langevin, MD,  Principal Investigator

Study chairs or principal investigators

Helene M. Langevin, MD,  Principal Investigator,  University of Vermont   

More Information

Study ID Numbers:  AT001121-01A1
Record last reviewed:  February 2005
Last Updated:  February 11, 2005
Record first received:  February 11, 2005
ClinicalTrials.gov Identifier:  NCT00103675
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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September 5, 2008



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