- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04896151
Assessing the Utility of MMPI-2-RF-EX in Detecting Simulated Underreporting of Current Suicide Risk in Military Veterans
October 4, 2023 updated by: Lauren Khazem, Ohio State University
The aim of the current project are is examine the incremental predictive utility of the MMPI-2-RF-EX validity scales in detecting simulated underreporting of suicide risk on the MMPI-2-RF-EX and other self-report measures of suicide risk in 150 military Veterans experiencing past-month death or suicidal ideation.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
75
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Craig Bryan, PsyD
- Phone Number: 614--366-2314
- Email: craig.bryan@osumc.edu
Study Locations
-
-
Ohio
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Columbus, Ohio, United States, 43214
- The Ohio State University
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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
Description
Inclusion Criteria:
- 18 years of age or older
- US military veteran
- death or suicidal ideation/suicide attempt within the past month
Exclusion Criteria:
- non-Veteran status
- acute intoxication or active psychosis precluding provision of informed consent
- an inability to communicate and comprehend English
- residence outside the United States
- lack of past-month death/suicide ideation or attempt
- younger than 18 years of age
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: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Standard MMPI
Participants will be instructed to complete the MMPI-2-RF-EX and other measures under standard conditions (e.g., to not simulate underreporting of suicide risk).
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The MMPI-2-RF-EX is a broadband, self-report measure of personality and psychopathology was developed for research purposes in order to develop the MMPI-3 (Ben-Porath & Tellegen, 2020), which is comprised of a subset of MMPI-2-RF-EX items.
Other Names:
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Experimental: Simulation MMPI
Participants will be instructed to conceal current suicide risk when completing the MMPI-2-RF-EX and other measures.
|
The MMPI-2-RF-EX is a broadband, self-report measure of personality and psychopathology was developed for research purposes in order to develop the MMPI-3 (Ben-Porath & Tellegen, 2020), which is comprised of a subset of MMPI-2-RF-EX items.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
MMPI-2-RF-EX Suicidal/Death Ideation scale
Time Frame: Baseline
|
The MMPI-2-RF-EX Suicidal/Death Ideation scale is a self-report measure of current suicide risk contained within the instrument.
T scores range from 45 to 100, with higher scores indicative of greater suicide risk.
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Baseline
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Beck Scale for Suicide Ideation (BSS)
Time Frame: Baseline
|
The BSS is a 21-item measure of past-week suicide ideation and desire for death.
Responses to items are scored on a 3-point Likert scale (range of 0- 2).
Scores range from 0 to 42, with higher scores indicating greater suicide risk.
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Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Suicide Cognitions Scale (SCS)
Time Frame: Baseline
|
The SCS is an 18-item survey measuring suicide-related thoughts and beliefs, unclouding hopelessness, perceived burdensomeness, entrapment, and unbearability.
Respondents rate their agreement with each statement on a 5-point Likert scale.
Scores range from 18-90, with higher scores indicating more severe suicide risk.
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Baseline
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Short Grit Scale
Time Frame: Baseline
|
The Short Grit Scale is an 8-item measure of trait-level perseverance and passion for long-term goals.
Possible scores range from 5 to 40, with higher scores indicting higher levels of grit.
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Baseline
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MMPI Posttest Inquiry (PTI)
Time Frame: Baseline
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The PTI assesses participants' compliance with condition-specific instructions for completing the MMPI and was adapted for the proposed research
|
Baseline
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PTSD Checklist for DSM-5 (PCL-5) PTSD Checklist for DSM-5
Time Frame: Baseline
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The PCL-5 is a self-report measure assessing the severity of 20 PTSD symptoms.
Scores range from 0 to 80, with higher scores indicating greater PTSD symptom severity.
|
Baseline
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Lauren Khazem, PhD, The Ohio State University Wexner Medical Center
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)
May 15, 2021
Primary Completion (Actual)
February 14, 2023
Study Completion (Actual)
February 14, 2023
Study Registration Dates
First Submitted
May 1, 2021
First Submitted That Met QC Criteria
May 17, 2021
First Posted (Actual)
May 21, 2021
Study Record Updates
Last Update Posted (Actual)
October 5, 2023
Last Update Submitted That Met QC Criteria
October 4, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020B0414
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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