The Accuracy of Manual Muscle Testing

June 16, 2017 updated by: Dr. Anne M. Jensen, Parker Research Institute

Investigating the Accuracy of Manual Muscle Testing for Distinguishing Congruent From Incongruent Statements Under Varying Levels of Blinding

Manual Muscle Testing (MMT) practiced by over a million practitioners worldwide. However, it's accuracy under varying levels of blindness has not yet been considered. This study will test this accuracy.

Study Hypothesis: MMT can accurately distinguish congruent from incongruent statements. Also, the accuracy of MMT is positively correlated with practitioner experience.

Study Overview

Status

Completed

Conditions

Detailed Description

Manual Muscle Testing is a non-invasive assessment tool used by millions of healthcare practitioners worldwide for a variety of purposes. First described in the literature by Lovett and Wight in 1915, MMT was originally used to assess muscular weakness in polio victims. In 1949, physiotherapists Kendall and Kendall refined MMT into an art and science with the publication of their benchmark text, Muscles: Testing and Function. This type of MMT is still used today to assess neuromuscular integrity.

In the 1960's, a different use for MMT was described by Dr. George Goodheart. In Goodheart's technique, called Applied Kinesiology (AK), MMT is used to evaluate a variety of additional functions of the body, apart from neuromuscular integrity. From Goodheart's work, many different techniques have emerged which use this second type of MMT. Moreover, it is estimated that over one million healthcare practitioners worldwide use this type of MMT: medical doctors, dentists, chiropractors, osteopaths, physiotherapists, other health professionals - plus even some lay-persons.

As a result of this divergence, there exists two very different forms of MMT: (1) orthopaedic muscle testing to quantify muscle strength and asses neurological integrity, and (2) the other type of muscle testing - which called be called "muscle response testing" which is used to obtain additional information about a patient. What that information is depends upon the MMT system being used and what information is sought. It is this latter form of MMT that this proposed study will investigate. Therefore, for the remainder of this application, the term "MMT" will be used to refer only to the second type ("muscle response testing").

The basic premise of MMT is that when there is some aberrant nervous system input to a muscle, it is less likely to be able to resist an external force. During a manual muscle test, an external force is applied to one muscle or group of muscles which at first causes an isometric then an eccentric contraction. Consequently, the muscle being tested is labelled "weak" or "strong" based on its ability to resist this external force.

A number of different techniques use MMT to test the body's physiological response to semantic stimuli, which may have both cognitive and emotional components. Monti et al. found that a MMT following congruent statements yielded significantly different results compared to a MMT following incongruent statements. A congruent statement is one that the person believes is true. An incongruent statement is one the person believes is false. The study by Monti et al. used self-referential statements similar to this study design, however they used statements such as, "My name is (insert one's name)". One criticism of using this type of self-referential statements is that in all likelihood both the muscle tester and the muscle testee know the verity of the statement, therefore, they are both unblinded, which may have introduced biased. While it is generally accepted by those who use this assessment tool that some bias exists in MMT, little is currently known about the degree of this bias. Therefore the main objective of this study is to investigate the accuracy of MMT to distinguish congruent from incongruent statements under varying degrees of blindness.

A further aim of this study are to explore if practitioner experience correlate with MMT accuracy. Caruso and Leisman reported greater MMT accuracy in experienced practitioners compared to inexperienced practitioners. Therefore, this study will test the reproducibility of these findings.

There will be two groups of participants selected for this study: (1) Practitioners, and (2) Testees - where the Practitioner will perform MMT on the Testee as the Testee speaks a statement. The Testee will know if s/he is speaking a true or false statement. However, for some statements, the Practitioner will be blind to the verity of the statement.

Results will be analysed for percent correct - that is, percent of muscle tests which accurately predicted the verity of the spoken statement.

Study Type

Observational

Enrollment (Actual)

160

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

    • Texas
      • Dallas, Texas, United States, 75229
        • Parker Research Institute

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 to 61 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

  1. Practitioenrs - Healthcare providers - healthy adults
  2. Testees - Healthy adults with no prior experience with MMT

Description

Inclusion Criteria:

  1. Practitioners

    • health care provider
    • aged between 18 and 65 years old
    • healthy
    • fluent in English
  2. Testees

    • aged between 18 and 65 years old
    • healthy
    • fluent in English

Exclusion Criteria:

  1. Practitioners

    • a current physical disability or injury of either upper extremity
    • Blind, deaf or mute
  2. Testees

    • a current physical disability or injury of either upper extremity
    • Prior experience with MMT
    • Blind, deaf or mute
    • are known to the Practitioner

NOTE: For this study, no compensation is possible.

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

  • Observational Models: Other
  • Time Perspectives: Other

Cohorts and Interventions

Group / Cohort
Practitioners
Healthcare practitioners who either use, have used or do not use MMT in practice
Testees
Healthy adults with no experience with MMT

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Percent correct
Time Frame: 1 hour
1 hour

Secondary Outcome Measures

Outcome Measure
Time Frame
Practitioner Experience
Time Frame: 1 hour
1 hour

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)

March 1, 2010

Primary Completion (Actual)

June 1, 2013

Study Completion (Actual)

June 1, 2013

Study Registration Dates

First Submitted

February 9, 2010

First Submitted That Met QC Criteria

February 9, 2010

First Posted (Estimate)

February 10, 2010

Study Record Updates

Last Update Posted (Actual)

June 19, 2017

Last Update Submitted That Met QC Criteria

June 16, 2017

Last Verified

June 1, 2017

More Information

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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