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Completed

NCT Number: NCT00699660

Enhancing Equitable and Effective (E-3) Post Traumatic Stress Disorder (PTSD) Disability Assessment

This project evaluated the impact of semi-structured, standardized interviews on the initial PTSD C&P on the examination.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Central Arkansas Veterans Healthcare System Eugene J. Towbin Healthcare Center, Little Rock, AR, North Little Rock, Arkansas, United States

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About this study

Our objective is to compare the process and outcomes of C&P exams for PTSD conducted with CAPS and WHODAS-II interviews versus the PTSD exams conducted without the CAPS and WHODAS-II interviews. This project will conduct a randomized controlled trial on 688 veterans to evaluate the effects of the CAPS/WHODAS instruments on the initial PTSD C&P examination process. Study outcomes include variation in assessing the DSM-IV components of PTSD, diagnostic accuracy, veteran perception of the exam process, VBA rater utility and resource utilization. This project will 1) demonstrate the feasibility of conducting program evaluation and intervention studies on the PTSD C&P examination process, 2) develop research tools, instruments and methods for C&P evaluation, 3) provide data on the value-added contribution of CAPS and WHODAS-II to the PTSD assessment process and examination report, and 4) inform the business case of utilizing the CAPS and WHODAS-II in the PTSD C&P process. The ultimate aim is to improve the reproducibility, consistency and validity of the PTSD examination process while maintaining a level of efficiency and cost restraint that provides veterans with an exam process that is fair, accurate and equitable across VHA.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Veterans referred to VHA for an Initial PTSD Compensation and Pension Examination
  • Informed consent

Exclusion criteria

  • Mentally impaired, not able to give informed consent
  • English speaking

Treatment and study plan

CAPS/WHODAS

Behavioral

CAPS/WHODAS structured clinical PTSD interview

Nonstructured Interview

Behavioral

Usual PTSD clinical PTSD interview, not CAPS or SCID

Other names: Usual Clinical Interview

Primary outcomes

  1. Completeness and Quality of PTSD Interview

    Time frame: Post-exam, same day

    total completeness of diagnostic assessment score, range from 0 to 100% and completeness of functional assessment

Secondary outcomes

  1. PTSD Diagnosis

    Time frame: Post-exam, same day

    Number of participants who were unable to receive a conclusive clinician PTSD diagnosis for positive or negative PTSD symptoms (unable to determine clinician diagnosis).

  2. Patient Satisfaction

    Time frame: post-exam, same day

    Mean score on satisfaction survey rating scale from 1 to 5 (higher)

  3. Resource Utilization

    Time frame: same day

    time spent administering the exam

Sponsors and collaborators

Lead sponsor

VA Office of Research and Development

Fed

Registry information

Official study title

Enhancing Equitable and Effective PTSD Disability Assessment

Acronym: E-3PTSD

Important dates

Study start
2009
Primary completion
2010
Study completion
2011
First posted
Jun 18, 2008
Registry last updated
Aug 16, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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