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Exploring Deployment Stress and Reintegration in Army National Guard Chaplains

Exploring Deployment Stress and Reintegration in Army National Guard Chaplains

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01330888
Enrollment
102
Registered
2011-04-07
Start date
2011-04-30
Completion date
2013-03-31
Last updated
2015-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Combat Stress Disorder

Keywords

war, religion, caregiver, combat stress disorder

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).

Interventions

None listed

Sponsors

US Department of Veterans Affairs
Lead SponsorFED

Study design

Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
observational2 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026