Encyclopedia of Psychology and Law

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diagnostic accuracy of the MCMI–III. Noteworthy in
the discussion of the diagnostic accuracy is the lack of
any information regarding the accuracy of the Thought
Disorder scale, a scale particularly relevant to crimi-
nal forensic practice.

Applicability and
Admissibility of the MCMI–III
The research to date suggests that the MCMI–III has
significant limitations for forensic practice in terms of
its ability to detect malingering and denial. Use of the
recommended VI > 1 criterion is likely to result in
inappropriate inclusion of random protocols in past
research studies and clinical interpretation of proto-
cols of questionable validity. The diagnostic accuracy
controversy remains an issue owing to methodologi-
cal flaws in the validation studies. The diagnostic
accuracy of the MCMI–III in the identification of Axis
I disorders is particularly underresearched. These are
important issues that must be considered in selecting
an assessment instrument not only from the perspec-
tive of the best measure for the forensic task but also
for the effect it will have on court proceedings, includ-
ing Daubert challenges to admissibility. One would
be wise to heed Robert Craig’s advice that a thorough
knowledge of the research supporting the test’s
applicability and limitations will best serve the inter-
ests of the client. In this regard, the paucity of studies
involving forensic populations; poor detection of
malingering, denial, and random responding; and the
diagnostic accuracy controversy are important issues
to be aware of. Experts are in agreement that the use
of the computer-generated report for the MCMI–III is
inappropriate because the sensitivity for detecting
pathology was artificially increased, resulting in over-
pathologizing of the respondent. All these issues need
to be resolved before the MCMI–III can be considered
a useful measure in forensic practice.

L. Thomas Kucharski and Joseph Toomey

See alsoForensic Assessment; Malingering

Further Readings
Craig, R. J. (1999). Testimony based on the Millon Clinical
Multiaxial Inventory: Review, commentary, and
guidelines. Journal of Personality Assessment,
73,290–304.

Daubert v. Merrell Dow Pharmaceuticals, Inc.,509 U.S. 579
(1993).
Dyer, F. J., & McCann, J. T. (2000). The Millon Clinical
Inventories, research criteria of their forensic application,
and the Daubert criteria. Law and Human Behavior,
24,487–497.
Rogers, R., Salekin, R. T., & Sewell, K. W. (1999). Validation
of the Millon Clinical Muliaxial Inventory for Axis II
disorders: Does it meet the Daubert standard. Law and
Human Behavior, 23,425–443.

MINNESOTAMULTIPHASIC


PERSONALITYINVENTORY–2


(MMPI–2)


The original Minnesota Multiphasic Personality
Inventory (MMPI) and its successor have been recog-
nized as the most widely used and researched objec-
tive clinical personality inventories. Using 567
true-false items, the MMPI–2 assesses a diverse range
of personality characteristics; symptoms of psy-
chopathology; and patterns of behavior, attitudes, and
concerns. First published in 1942 and revised in 1989,
the instrument yields a wealth of clinical data and is
used across multiple clinical and medical settings, for
employment screening and selection, and in a variety
of forensic situations.
The test includes multiple validity indices, assess-
ing test-taking attitudes and approach; 10 basic,
numbered clinical scales (1 =Hypochondriasis, 2 =
Depression, 3 =Hysteria, 4 =Psychopathic Deviate,
5 = Masculinity-Femininity, 6 = Paranoia, 7 =
Psychasthenia, 8 =Schizophrenia, 9 =Hypomania, 0 =
Social Introversion,with all but scales 5 and 0 consid-
ered core clinical scales) and their subscales; as well as
more than five dozen content scales (e.g., Antisocial
Practices, Anxiety), content component scales (e.g.,
Negative Treatment Indicators: Low Motivation),
personality psychopathology trait scales (e.g., Aggres-
siveness, Negative Emotionality/Neuroticism), and
supplementary scales (e.g., Addiction Potential,
Overcontrolled-Hostility).
Raw scores on these scales are transformed to
norm-based T-scores (mean =50, standard deviation
= 10) to enhance the interpretability of results.
Scales with a T-score of 65 or greater are considered
clinically significant. In addition to interpretive

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