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Combat Stress DisorderNCT01330888

Exploring Deployment Stress and Reintegration in Army National Guard Chaplains

An observational study of Combat Stress Disorder, run by US Department of Veterans Affairs at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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). Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Combat Stress Disorder
How many people
102 participants
Where
1 siteUnited States
Study dates
Apr 2011to Mar 2013
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: ARNG Chaplains who have ever/never been deployed to OEF/OIF combat theaters

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

United States1 site
  • James A. Haley Veterans' Hospital

    Tampa, Florida, 33637-1022

Other trials in United States

About this study

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).

Keywords
war, religion, caregiver, combat stress disorder
Medical subject headings
Combat Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01330888
Study groupRoleWhat they receive
Group 1ARNG Chaplains

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. observational

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Apr 2011 (estimated)
  2. Study startApr 2011
  3. Primary completionMar 2013
  4. Study completionMar 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Time perspective
Cross-sectional
Enrolment
102 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01330888
Sponsor's protocol ID
D7800-P
Status last verified
Feb 2015
First submitted
5 Apr 2011
Last updated
19 Feb 2015
Results posted
No
Data monitoring committee
No

Publications

  • 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.

    PubMed 23094615
  • 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. doi: 10.7205/milmed-d-12-00071.

    PubMed 23025131

Questions about this trial

What is this clinical trial studying?

An observational study of Combat Stress Disorder, run by US Department of Veterans Affairs at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Feb 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

observational (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01330888, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Feb 2015.

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