Providing Mental Health Services to Operation Iraqi Freedom (OIF)/Operation Enduring Freedom (OEF) Veterans

June 8, 2015 updated by: Gina Signoracci, VA Eastern Colorado Health Care System

Providing Mental Health Services to Operation Iraqi Freedom (OIF)/Operation Enduring Freedom (OEF) Veterans: Provider Perspectives

The purpose of this study is to gather information from VISN 19 Denver VA mental health professionals regarding their perspectives of necessary resources to provide best practice mental health service to Operation Iraqi Freedom (OIF)/ Operation Enduring Freedom (OEF) Veterans. Specifically, this study aims to describe provider perspectives regarding the following: a) clinical needs of OIF/OEF Veterans; b) collaboration and referral processes; c) barriers to providing optimal treatment to this cohort d) provider needs and resources that may improve service delivery to this cohort; e) provider perspectives regarding psychiatric outcomes in this cohort; and f) professional satisfaction. Support for this study is provided by previous research evaluating Veteran's Administration (VA) needs to provide service to OIF/OEF Veterans (Sayer, et al. 2009; Friedmann-Sanchez, et al. 2008).

The above information will be obtained using semi-structured interview. Hypotheses are not provided as this is an exploratory qualitative study.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

No hypotheses are associated with this study as this is a qualitative study wherein subjects will participate in a semi-structured interview developed specifically for this study, which serves as the outcome measure. Up to 30 providers will be interviewed.

Data Analysis Interviews will be transcribed in their entirety and de-identified. Dr. Signoracci and 4 additional MRIECC researchers will independently code each interview for themes. Finally, group meetings with Dr. Signoracci and MIRECC researchers will be held in order to achieve larger consensus regarding such unique and universal themes (Rubin & Rubin, 1995).

Any reporting of information regarding: a) length of time employed at Denver VA; b) length of time employed within VA system; c) provider professional title; d) provider degree; f) professional licenses held; g) clinic/service in which provide services will be done in the aggregate, across clinics. No individual data will be reported with respect to these items. Also, any selected quotes that are reported will remain de-identified.

Power analyses will not be conducted because no hypothesis quantitative testing is being done, and therefore there are no parameters to estimate. With qualitative designs one conducts interviews until reaching the saturation point. In other words, subsequent interviews do not yield any new information (Rubin & Rubin, 1995). Previous experience (Brenner et al., 2008) suggests that 25 completed interviews should provide a wide enough range of responses for important themes to emerge.

Study Type

Observational

Enrollment (Actual)

13

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

  • United States
    • Colorado
      • Denver, Colorado, United States, 80220
        • Denver VA

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 to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Denver VA Mental Health Providers Up to 30 providers will be interviewed.

Description

Inclusion Criteria

  • Denver VA Mental Health Providers that provide mental health treatment to OIF/OEF Veterans
  • Age 18-70

Exclusion Criteria Denver VA providers that do not provide mental health to OIF/OEF Veterans

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Denver VA OIF/OEF and mental health providers
Other: No Intervention
No Intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Semi-Structured Interview
Time Frame: Interview conducted one time per participant (completion time: approximately 1 hour)
Semi-structured interview regarding provider experiences of providing mental health treatment to OIF/OEF Veterans. The interview takes approximately 1 hour to complete and is conducted one time with each participant.
Interview conducted one time per participant (completion time: approximately 1 hour)

Collaborators and Investigators

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

Sponsor

VA Eastern Colorado Health Care System

Investigators

  • Principal Investigator: Gina M Signoracci, Ph.D., VISN 19 Denver VA MIRECC

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

July 1, 2011

Primary Completion (Actual)

July 1, 2012

Study Completion (Actual)

March 1, 2014

Study Registration Dates

First Submitted

November 7, 2011

First Submitted That Met QC Criteria

November 17, 2011

First Posted (Estimate)

November 22, 2011

Study Record Updates

Last Update Posted (Estimate)

June 9, 2015

Last Update Submitted That Met QC Criteria

June 8, 2015

Last Verified

June 1, 2015

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 11-0300

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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