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Instrument Applied and Manual Manipulation Induced EMG Response in Asymptomatic Subjects

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2007 by Logan College of Chiropractic.
Recruitment status was:  Recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00378963
First Posted: September 21, 2006
Last Update Posted: August 1, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Logan College of Chiropractic
  Purpose
The purpose of this study is to determine the affects of instrumental and manual manipulation on the EMG response of asymptomatic subjects.

Condition Intervention
EMG Response Device: ProAdjuster

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)

Further study details as provided by Logan College of Chiropractic:

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   20 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

Asymptomatic subjects (without somatosensory peripheral pain) will be recruited in the study. Subjects must sign an informed consent.

Exclusion Criteria:

Subjects with heart failure and any nervous system diseases will be excluded from the study. Additional exclusions include osteoporosis, diabetes, pregnancy, vascular insufficiency, and history of joint replacement therapy. Subjects under medical treatment, surgery and trauma within six months will be excluded.

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00378963


Contacts
Contact: John Zhang, MD, PhD 636-227-2100 ext 1920 john.zhang@logan.edu
Contact: Rodger Tepe, PhD 636-227-2100 ext 1952 rodger.tepe@logan.edu

Locations
United States, Missouri
Logan College of Chiropractic Recruiting
Chesterfield, Missouri, United States, 63017
Contact: John Zhang, MD, PhD    636-221-2700 ext 1920    john.zhang@logan.edu   
Sponsors and Collaborators
Logan College of Chiropractic
Investigators
Principal Investigator: John Zhang, MD, PhD Logan College of Chiropractic
  More Information

Additional Information:
Publications:
ClinicalTrials.gov Identifier: NCT00378963     History of Changes
Other Study ID Numbers: RD0606060022
First Submitted: September 18, 2006
First Posted: September 21, 2006
Last Update Posted: August 1, 2007
Last Verified: May 2007