Basic and Balance: Logan Basic Technique on Bilateral Weight Balance

August 21, 2008 updated by: Logan College of Chiropractic

The Effects of Logan Basic Technique on Bilateral Weight Balance

This is an experimental study to examine whether a chiropractic intervention (specifically Logan Basic Technique) can help restore balance distribution in individuals with or without vertebral subluxations.

Study Overview

Detailed Description

Postural imbalance caused by abnormal weight distribution in the body may cause discomfort, pain and deformity. In the human body, weight and the resistance to gravity is controlled by the bones that make up the skeletal system which are supported by ligaments and tendons. Without this framework holding up upright, we would fall to the ground due to the external forces of gravity. When one half of the body must work harder to support more weight than the other, the half of the body with the greater imbalance may become strained. As a result of the imbalance, strain and tension will increase causing a decrease in blood supply which will decrease proper exchange of wastes, nutrients, and oxygen causing an increase in toxicity. According to the Logan Basic Methods textbook, as long as there remains a symptom of strain in muscle tissue as a result of abnormalities of the body framework, such a muscle is capable, with slight assistance, of restoring its subluxated attachments to their normal relationship. The slightest force exerted on either of its attachments, directly or indirectly, tends to approximate its points of attachment and result in a decreased strain of the muscle. Therefore, the necessary amount of force applied to improve postural distortion is dependent upon the nature or degree of the patient's postural distortion or muscular imbalance.

The system of Logan Basic Methods uses structural analysis from radiography combined with postural and clinical examination findings to determine and apply specific low-force adjustments to the pelvis and spine. The most commonly applied contact of Logan Basic Technique, the apex contact, specifically contacts the sacrotuberous ligament, which connects the ischial tuberosity to the anterior aspect of the sacrum, as it attaches to the sacrum. This ligament is believed to play an integral role in the stability of the pelvis, especially during nutation and counter-nutation. This is further evidenced by a study of the function of the long dorsal sacroiliac ligament, of which the sacrotuberous ligament played a significant role in counter-balancing the pelvis during nutation and counter-nutation.

The Midot Postural Analyzer QPS-200 provides data regarding weight distortion of the actual body weight within a 360 degree radius, in a two dimensional plane.

Similar studies have been performed by Logan students in the past. The first study found, from 1990, was designed as a double blind study with apex contacts or sham adjustments given to participants in an attempt to determine affects of Logan Basic Technique on leg length deficiency and balance. Only one adjustment was given to each participant. Results were inconclusive, with no favorable results for the intervention. Another similar study performed in 1996 by Goutlet, Webb, and Lawson under the guidance of Dr. Brian Snyder was a double blind study that used an apex contact for the experimental intervention and a sham adjustment for the control group. The researchers used two common bathroom scales for their data collection. A positive correlation was found between the weight distribution changes pre-post adjustment in the experimental group, with only one treatment given to subjects in the study.

Study Type

Interventional

Enrollment (Anticipated)

75

Phase

  • Phase 2

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

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Participants will be limited to Logan College of Chiropractic students.
  • Have an initial imbalance in their weight distribution of greater than 4 pounds.

Exclusion Criteria:

  • Pregnant
  • Persons with an imbalanced structural scoliosis, which will be determined by the utilization of a posterior plumb line.
  • Taking herbs or medication that affects balance
  • Individuals with problems maintaining their balance as seen in Meniere's syndrome, otitis interna and otitis media
  • Individual diagnosed Diabetes
  • Individuals currently receiving any spinal manipulation

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: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental Group
A Logan Basic Apex Contact, which is a contact that is placed on the anterior surface of the sacrotuberous ligament with a light force directed posterior with varying degrees of laterality.
A Logan Basic Apex Contact, which is a contact that is placed on the anterior surface of the sacrotuberous ligament with a light force directed posterior with varying degrees of laterality.
Sham Comparator: Sham Group
light force contact applied to the inferior surface of the sacrotuberous ligament, directed straight superiorly.
light force contact applied to the inferior surface of the sacrotuberous ligament, directed straight superiorly.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
weight distribution
Time Frame: before and after treatment, 3 times over 3 days
before and after treatment, 3 times over 3 days

Secondary Outcome Measures

Outcome Measure
Time Frame
center of gravity
Time Frame: before and after treatment, 3 times over 3 days
before and after treatment, 3 times over 3 days

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

June 1, 2008

Primary Completion (Actual)

August 1, 2008

Study Completion (Actual)

August 1, 2008

Study Registration Dates

First Submitted

August 21, 2008

First Submitted That Met QC Criteria

August 21, 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 21, 2008

Last Verified

August 1, 2008

More Information

Terms related to this study

Other Study ID Numbers

  • SR0225080130

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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