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Logan Basic and Dysmenorrhea
This study is currently recruiting participants.
Verified by Logan College of Chiropractic, August 2008
Sponsored by: Logan College of Chiropractic
Information provided by: Logan College of Chiropractic
ClinicalTrials.gov Identifier: NCT00740818
  Purpose

The purpose of this study is to determine the effects of Logan Basic Technique on symptoms of dysmenorrhea.


Condition Intervention Phase
Menstrual Distress (Dysmenorrhea)
Other: No Intervention
Procedure: Sham Logan Basic Adjustment
Procedure: Logan Basic adjustment
Phase II

MedlinePlus related topics: Menstruation
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Single Blind (Outcomes Assessor), Parallel Assignment, Safety/Efficacy Study
Official Title: A Pilot Study: Logan Basic Technique and Auxiliary Abdominal Contacts for Reducing Symptomatology of Primary Dysmenorrhea

Further study details as provided by Logan College of Chiropractic:

Primary Outcome Measures:
  • Menstrual Distress Questionnaire [ Time Frame: Before and after treatment ] [ Designated as safety issue: No ]

Estimated Enrollment: 30
Study Start Date: July 2008
Estimated Study Completion Date: November 2008
Estimated Primary Completion Date: November 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
A: No Intervention
The patient will lay prone on the adjustment table 5 minutes, the approximate equivalency of a Logan Basic adjustment. Table will be in proper position according to Logan Basic protocol.
Other: No Intervention
The patient will lay prone on the adjustment table 5 minutes, the approximate equivalency of a Logan Basic adjustment. Table will be in proper position according to Logan Basic protocol.
B: Sham Comparator
A thumb contact will be used against the sacrotuberous ligament as opposed to underneath the ligament. Auxiliary contacts will also be sham adjustments; the spine will be contacted but no force applied.
Procedure: Sham Logan Basic Adjustment
A thumb contact will be used against the sacrotuberous ligament as opposed to underneath the ligament. Auxiliary contacts will also be sham adjustments; the spine will be contacted but no force applied.
C: Experimental
Logan Basic adjustment, as well as auxiliary and abdominal contacts, based on the Logan Basic protocol.
Procedure: Logan Basic adjustment
Logan Basic adjustment, as well as auxiliary and abdominal contacts, based on the Logan Basic protocol.

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Female Logan students, staff, or faculty
  • Minimum of 18 years
  • No chiropractic adjustments below T12 throughout the duration of the study
  • Suffering from primary dysmenorrhea

Exclusion Criteria:

  • Pregnancy
  • Endometriosis (if known to have)
  • Reproductive cancer of any kind
  • NSAIDs and/or any other medical or herbal treatments for symptoms of dysmenorrhea. Oral contraception use for this purpose will not be excluded from the study; however, usage will be noted in the final reporting of this study's results.
  • Menopause
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00740818

Contacts
Contact: Patrick Montgomery, DC 636-230-2100 ext 1931 patrick.montgomery@logan.edu

Locations
United States, Missouri
Logan University, College of Chiropractic Recruiting
Chesterfield, Missouri, United States, 63017
Sponsors and Collaborators
Logan College of Chiropractic
  More Information

Responsible Party: Logan College of Chiropractic ( Patrick Montgomery, DC )
Study ID Numbers: SR1120070131
Study First Received: August 21, 2008
Last Updated: August 22, 2008
ClinicalTrials.gov Identifier: NCT00740818  
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Signs and Symptoms
Pelvic Pain
Menstruation Disturbances
Dysmenorrhea
Pain

Additional relevant MeSH terms:
Pathologic Processes

ClinicalTrials.gov processed this record on January 16, 2009