Logan Basic and Dysmenorrhea

August 22, 2008 updated by: Logan College of Chiropractic

A Pilot Study: Logan Basic Technique and Auxiliary Abdominal Contacts for Reducing Symptomatology of Primary Dysmenorrhea

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

Study Overview

Detailed Description

Dysmenorrhea, also known in the public realm as the dreaded painful period, is a common condition plaguing millions of women. The familiar symptoms of dysmenorrhea include but are not limited to muscle cramping of the lower abdominal muscles, mood swings, breast tenderness, and heavy flow just to name a few. These common complaints can range from a minor annoyance to debilitating. The allopathic model of medicine has offered up several solutions to this problem most women face during their reproductive phase of life. However, even with these options for menstrual discomfort relief, the problem still remains in overwhelming numbers. The rationale of this study is to possibly provide another safer and more effective treatment using protocols of chiropractic medicine.

According to Merck, dysmenorrhea is simplified as pelvic pain during menses. This condition can also be broken down into two forms-primary dysmenorrhea and secondary dysmenorrhea. Primary dysmenorrhea tends to begin in adolescence with the onset of menses. This form is attributed to histological and hormonal changes to the female reproductive system. The symptoms tend to subside with age and pregnancy. Secondary dysmenorrhea is seen to develop in the adult female and is linked to structural anomalies of the pelvic region. Although both of these cause discomfort to several women, the main focus of this study is on treatment of primary dysmenorrhea as treatment of the secondary form involves addressing the underlying structural dysfunction causing the symptoms. This is out of the scope of this study.

Medical treatment of dysmenorrhea involves a few different facets. The first approach is to treat the symptoms of dysmenorrhea with the use of analgesics which is usually the most popular and convenient option. These medications are over-the-counter and are often effective treatment in mild cases. Another option commonly pursued in the medical realm is addressing the hormonal imbalances involved in symptomatology. This is done by prescribing the use of low dose oral contraceptives. This treatment is popular as it provides a convenient preventative measure for pregnancy in addition to symptom relief in some cases. Surgery, an extreme and last resort, involves anywhere from partial to a complete hysterectomy. With partial hysterectomies, there is a higher risk that symptoms will still be present following surgery. However, following a full hysterectomy the patient is subject to the adverse effects of post menopause including but not limited to increased bone loss.

Although effective in the treatment of dysmenorrhea, the medical options can produce adverse effects on the body. Chiropractic treatment offers a mode of care with limited risks and many benefits to the patient. It is the goal of this study to aid in the support of this statement. It has been documented that spinal manipulation using Flexion-Distraction technique combined with Manual Trigger Point therapy has positive results with short-term relief of symptomatology and disability related to chronic pelvic pain syndrome, which is defined as noncyclic pain in the pelvis lasting longer than three months. Although this condition is separate from dysmenorrhea it can provide some insight into symptomatology affecting this region. The Toftness system has also demonstrated significant improvement in subjects suffering from primary dysmenorrhea when compared to those subjects receiving sham adjustments. Gauntt demonstrated the benefits of Logan Basic Technique and Soft Tissue Manipulation in decreasing the symptoms of painful periods. The combination of these treatments establishes "great promise" in intervention of dysmenorrhea. The goal of this new study is to build on Gauntt's work by possibly duplicating these results. This study also aims to explore the efficacy of utilizing auxiliary abdominal contacts in addition to the Logan Basic Protocols.

Logan Basic Methods of adjusting addresses the correction of the base of the spine, the sacrum. By contacting the sacrotuberous ligament on the side of the anteriorly and inferiorly misaligned sacrum, the doctor corrects the said misalignment to help restore proper function to the affected sacroiliac joint. Furthermore, correction of the foundation of the spine, according to Logan Basic Methods, restores optimum function to the entire spine. To increase the efficacy of this procedure, known as the apex contact, one can also utilize auxiliary contacts. Auxiliary contacts are administered during the apex contact. Specifically, auxiliary abdominal contacts address hollow organ spasms. This may be beneficial in addressing the uterine muscle spasms commonly associated with menses.

Logan Basic encompasses a low force adjusting protocol which can be helpful in treatment of all types of patients. This technique is essentially safe for everyone with no known contraindications. However, with any adjusting technique there are adverse reactions to treatment, although usually minor. Patients can experience increased perspiration with their first few adjustments. Following adjustments, the patient can experience pain associated with muscle soreness, which can be treated with the use of cold compresses for twenty minutes on then twenty minutes off for the first 48 hours after treatment. Muscle soreness usually subsides within a day or two and its occurrence decreases with subsequent treatments. Some patients may experience a toxic reaction to treatment that is described as nausea and/or vomiting. This occurs in individuals with increased exposure to drugs and/or a poor diet. However, it is believed that though this reaction has occurred, these patients were in need of this intervention to eliminate toxins from the body.

For this study, a menstrual distress questionnaire will be utilized to objectively analyze subjective complaints of subjects in this study. This method of analyzing symptoms has been used in past studies including Snyder's study on the Toftness system and dysmenorrhea as well as in Gauntt's study on Logan Basic, Soft Tissue Manipulation, and dysmenorrhea. Moos provides an overview of the utilization of this questionnaire. It has been shown to be quite useful in studies with menstrual distress.

Through the exploration of Logan Basic Methods and auxiliary abdominal contacts in the treatment of dysmenorrhea, it is the hope of the investigators to provide some insight into this common condition affecting and disabling women. This investigation aims to build on previous studies showing the efficacy of chiropractic care in the treatment of menstrual distress. Through investigation of primary dysmenorrhea, this study can hopefully assist in opening the scientific community as well as the females of the current society to safer options in treatment of this common condition.

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Missouri
      • Chesterfield, Missouri, United States, 63017
        • Recruiting
        • Logan University, College of Chiropractic

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
NO_INTERVENTION: A
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.
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.
SHAM_COMPARATOR: B
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.
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.
EXPERIMENTAL: C
Logan Basic adjustment, as well as auxiliary and abdominal contacts, based on the Logan Basic protocol.
Logan Basic adjustment, as well as auxiliary and abdominal contacts, based on the Logan Basic protocol.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Menstrual Distress Questionnaire
Time Frame: Before and after treatment
Before and after treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2008

Primary Completion (ANTICIPATED)

November 1, 2008

Study Completion (ANTICIPATED)

November 1, 2008

Study Registration Dates

First Submitted

August 21, 2008

First Submitted That Met QC Criteria

August 22, 2008

First Posted (ESTIMATE)

August 25, 2008

Study Record Updates

Last Update Posted (ESTIMATE)

August 25, 2008

Last Update Submitted That Met QC Criteria

August 22, 2008

Last Verified

August 1, 2008

More Information

Terms related to this study

Other Study ID Numbers

  • SR1120070131

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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