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Prolonged Grief and Suicide Among Veterans

This study has been withdrawn prior to enrollment.
(Study should not have been listed on ClinicalTrials.gov)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01247025
First Posted: November 24, 2010
Last Update Posted: March 26, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
University of Colorado, Denver
Information provided by:
VA Eastern Colorado Health Care System
  Purpose
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.

Condition Intervention
Prolonged Grief Disorder Suicidality Other: No intervention

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Examining Prolonged Grief Disorder and Its Relationship to Self-Directed Violence Among Veterans

Resource links provided by NLM:


Further study details as provided by VA Eastern Colorado Health Care System:

Primary Outcome Measures:
  • Prolonged Grief Disorder- 13 [ Time Frame: At least six months post-bereavement ]

Secondary Outcome Measures:
  • Adult Suicidal Ideation Questionnaire [ Time Frame: Within past month ]

Enrollment: 0
Study Start Date: November 2010
Estimated Study Completion Date: August 2011
Primary Completion Date: April 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Veterans
Veterans receiving mental health services at the Eastern Colorado Healthcare System (ECHCS)/Denver Veterans Affairs Medical Center (VAMC)
Other: No intervention
This study will not contain a specific intervention

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
The participants in this observational study will be all individuals willing and eligible among those seeking outpatient mental health services at the Eastern Colorado Healthcare System (ECHCS)/Denver Veterans Affairs Medical Center (VAMC). It is expected that 180 participants will be enrolled in an effort to obtain up to 150 completed protocols. Women and minorities will be recruited as a routine part of the study. However, given the participant population within the Eastern Colorado Healthcare System (ECHCS)/Denver Veterans Affairs Medical Center (VAMC), it is expected the majority of participants will be Caucasian men.
Criteria

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.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01247025


Locations
United States, Colorado
Eastern Colorado Health Care System (ECHCS) / Denver VA Medical Center
Denver, Colorado, United States, 80220
VA Eastern Colorado Health Care System
Denver, Colorado, United States, 80220
Sponsors and Collaborators
VA Eastern Colorado Health Care System
University of Colorado, Denver
Investigators
Principal Investigator: Peter M Gutierrez, PhD VA Eastern Colorado Health Care System
  More Information

Responsible Party: Peter M. Gutierrez, Ph.D./ Clinical research Psychologist, VA VISN 19 MIRECC
ClinicalTrials.gov Identifier: NCT01247025     History of Changes
Other Study ID Numbers: jrings1
First Submitted: November 22, 2010
First Posted: November 24, 2010
Last Update Posted: March 26, 2014
Last Verified: March 2014