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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01247025
Other study ID # jrings1
Secondary ID
Status Withdrawn
Phase N/A
First received November 22, 2010
Last updated March 21, 2014
Start date November 2010
Est. completion date August 2011

Study information

Verified date March 2014
Source VA Eastern Colorado Health Care System
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardUnited States: Federal Government
Study type Observational

Clinical Trial Summary

The primary research question in this study will ask, among those receiving outpatient mental health services (MHS) at the Eastern Colorado Healthcare System (ECHCS)/Denver Veterans Affairs Medical Center (VAMC), how many suffer from Prolonged Grief Disorder (PGD)? Here, it is hypothesized that PGD will occur within the sample. A secondary aim of this study will be to investigate how often PGD co-occurs with posttraumatic stress disorder (PTSD) and/or depression. Also, while PGD has been shown to have an effect on self-directed violence (SDV) among civilians (Prigerson, Bridge et al., 1999), no studies yet have examined the relationship between PGD and SDV among Veterans. Therefore, it also is hypothesized that as PGD severity increases among the Veteran sample, risk for SDV will increase as well. Additional research aims also will be addressed in this study. For one, it will be assessed which grief symptoms are most often reported among the Veteran sample. Also, no study has yet to examine if there are neuropsychological differences between PGD and PTSD. Therefore, another research question here is whether PGD indeed is neuropsychologically different from PTSD. Here, the exploratory hypothesis is that PGD sufferers will respond to a measure of multiple components of cognition (e.g., planning, sequencing, concentration, multitasking, and memory efficiency) in a manner that is significantly different from PTSD sufferers.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 2011
Est. primary completion date April 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age 18 and above

- Not currently active duty in any branch of the military

- English-speaking

- Ability to adequately respond to specific questions regarding the informed consent procedure.

- Active case in Mental Health Services (MHS) at the Eastern Colorado Healthcare System (ECHCS)/Denver Veterans Affairs Medical Center (VAMC)

Exclusion Criteria:

- Currently active duty in any branch of the military

- Non-English-speaking

- Inability to adequately respond to questions regarding the informed consent procedure.

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Other:
No intervention
This study will not contain a specific intervention

Locations

Country Name City State
United States Eastern Colorado Health Care System (ECHCS) / Denver VA Medical Center Denver Colorado
United States VA Eastern Colorado Health Care System Denver Colorado

Sponsors (2)

Lead Sponsor Collaborator
VA Eastern Colorado Health Care System University of Colorado, Denver

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prolonged Grief Disorder- 13 At least six months post-bereavement No
Secondary Adult Suicidal Ideation Questionnaire Within past month Yes
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