MedPath

Exploring Deployment Stress and Reintegration in Army National Guard Chaplains

Completed
Conditions
Combat Stress Disorder
Registration Number
NCT01330888
Lead Sponsor
US Department of Veterans Affairs
Brief Summary

The purpose of this 2-year pilot study is to explore the impact of deployment on the psychosocial and health characteristics and reintegration of Military Chaplains, specifically those of the Army National Guard (ARNG). This pilot will serve as the foundation for subsequent investigations of chaplains from multiple branches of the military. In addition to spiritual and religious support, Military Chaplains play a key role in the behavioral health of deployed service-members, routinely participating in suicide prevention training, conducting critical event debriefing, and identifying service-members at risk for combat and operational stress reactions1. A high risk group for exposure to trauma2, Military Chaplains have suffered brain injuries, gunshot wounds and blast injuries in OEF/OIF Theater3. In addition, many report combat related stress issues such as compassion fatigue, PTSD, and reintegration issues3. While the traumatic experiences of OEF/OIF deployed troops have been well documented, the effects on military chaplains caring for these service-members have received little attention in the research to date. We are collaborating with the National Guard Chaplain Corps Leadership on this program of research. The aims of this 2-year pilot cross-sectional study focus on describing and exploring deployment and its impact on psychosocial, health characteristics and reintegration of ARNG chaplains using a mixed method approach (web-based survey, in-depth interviews, social network analysis).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
102
Inclusion Criteria
  • current, active members of ARNG during timeframe of OIF/OEF/OND
  • Chaplains
  • able to be contacted by email for survey explanation and participation
  • consent to participate in interview or network questionnaire
Exclusion Criteria
  • not current, active members of ARNG during timeframe of OIF/OEF/OND
  • not Chaplains
  • not able to be contacted by email for survey explanation and participation
  • do not consent to participate in interview or network questionnaire

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
observational2 years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

James A. Haley Veterans' Hospital

🇺🇸

Tampa, Florida, United States

© Copyright 2025. All Rights Reserved by MedPath