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A Pilot Investigational Study: Treatment of Anxiety With Non-Needle Electro-Acupuncture

This study has been completed.

Sponsored by: Logan College of Chiropractic
Information provided by: Logan College of Chiropractic
ClinicalTrials.gov Identifier: NCT00335946
  Purpose

The purpose of this study is to determine the effects of non-needle electro-acupuncture on mild to moderate anxiety. The hypothesis is that this style of treatment will reduce state anxiety and not trait anxiety as measured by the Spielberger STAI test.


Condition Intervention Phase
Anxiety, Mild to Moderate
Device: HANS non-needle acupuncture
Procedure: Stimulation of two acupuncture points bi-lateral
Phase I

MedlinePlus related topics:   Acupuncture    Anxiety   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study

Further study details as provided by Logan College of Chiropractic:

Primary Outcome Measures:
  • Spielberger STAI test

Estimated Enrollment:   40
Study Start Date:   June 2006
Study Completion Date:   December 2006

Detailed Description:

Persistent and unrelenting stress is defined as anxiety. Anxiety disorders are among the most common mental disorders in society. The NIH estimates that nearly 200 million Americans suffer from anxiety. Anxiety disorders are associated with a lower quality of life, functional impairment and disability, and are also associated with co-morbid physical illness.

Acupuncture, one form of complementary and alternative medicine, has been used to treat anxiety. Non-needle acupuncture is one of the safest methods, with none to rare side effects. This method has been studied in China (Han 1986) and America (Ulett 1998) Pre-intervention testing, then three treatments within one week, will be followed by post intervention testing.

  Eligibility
Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria: Normally healthy persons with mild to moderate anxiety -

Exclusion Criteria: Severe anxiety, depression, pregnancy, and previous experience with HANS non-needle electro-acupuncture treatment

-

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00335946

Locations
United States, Missouri
Logan College of Chirpractic    
      Chesterfield, Missouri, United States, 63017

Sponsors and Collaborators
Logan College of Chiropractic

Investigators
Principal Investigator:     David V. Beavers, DC     Logan College of Chiropractic    
  More Information


Publications:

Study ID Numbers:   RD0602060019
First Received:   June 8, 2006
Last Updated:   July 31, 2007
ClinicalTrials.gov Identifier:   NCT00335946
Health Authority:   United States: Institutional Review Board

ClinicalTrials.gov processed this record on October 14, 2008




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