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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01330888
Other study ID # D7800-P
Secondary ID
Status Completed
Phase N/A
First received April 5, 2011
Last updated February 18, 2015
Start date April 2011
Est. completion date March 2013

Study information

Verified date February 2015
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial 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).


Recruitment information / eligibility

Status Completed
Enrollment 102
Est. completion date March 2013
Est. primary completion date March 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility 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

Time Perspective: Cross-Sectional


Locations

Country Name City State
United States James A. Haley Veterans' Hospital Tampa Florida

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

References & Publications (2)

Besterman-Dahan K, Barnett S, Hickling E, Elnitsky C, Lind J, Skvoretz J, Antinori N. Bearing the burden: deployment stress among army national guard chaplains. J Health Care Chaplain. 2012;18(3-4):151-68. doi: 10.1080/08854726.2012.723538. — View Citation

Besterman-Dahan K, Gibbons SW, Barnett SD, Hickling EJ. The role of military chaplains in mental health care of the deployed service member. Mil Med. 2012 Sep;177(9):1028-33. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary observational 2 years No