Exploring Deployment Stress and Reintegration in Army National Guard Chaplains
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Purpose
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).
| Condition |
|---|
|
Combat Stress Disorder |
| Study Type: | Observational |
| Study Design: | Time Perspective: Cross-Sectional |
| Official Title: | Exploring Deployment Stress and Reintegration in Army National Guard Chaplains |
- observational [ Time Frame: 2 years ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 266 |
| Study Start Date: | April 2011 |
| Study Completion Date: | March 2013 |
| Primary Completion Date: | March 2013 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
Group 1
ARNG Chaplains
|
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
ARNG Chaplains who have ever/never been deployed to OEF/OIF combat theaters
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
Contacts and Locations| United States, Florida | |
| James A. Haley Veterans Hospital | |
| Tampa, Florida, United States, 33637-1022 | |
| Principal Investigator: | Karen Besterman-Dahan, PhD MA BS | James A. Haley Veterans Hospital |
More Information
Publications:
| Responsible Party: | Department of Veterans Affairs |
| ClinicalTrials.gov Identifier: | NCT01330888 History of Changes |
| Other Study ID Numbers: | D7800-P |
| Study First Received: | April 5, 2011 |
| Last Updated: | May 15, 2013 |
| Health Authority: | United States: Federal Government |
Keywords provided by Department of Veterans Affairs:
|
war religion caregiver combat stress disorder |
Additional relevant MeSH terms:
|
Stress Disorders, Traumatic Combat Disorders Anxiety Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 23, 2013