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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01652443
Other study ID # 11-0488
Secondary ID
Status Completed
Phase N/A
First received December 28, 2011
Last updated May 12, 2017
Start date April 2011
Est. completion date July 2016

Study information

Verified date May 2017
Source VA Eastern Colorado Health Care System
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The current study will explore relationships and health in the OEF/OIF Veteran population. Specifically, this study will examine PTSD symptom severity, traumatic brain injury, relationship satisfaction, leisure, general health ratings, feelings of burdensomeness and belongingness, and suicidal ideation.


Description:

United States military troops returning home from Operation Enduring Freedom and Operation Iraqi Freedom deployments are presenting with "invisible wounds". These "invisible wounds" include mental health conditions such as posttraumatic stress disorder and traumatic brain injury. Recent literature has begun to explore how PTSD affects the service member, as well as their significant others. Several studies have shown that Veteran endorsement of PTSD symptoms is associated with decreased relationship satisfaction. Prior literature has shown that spending time together and engaging in pleasurable activities as a couple are important strategies for enduring relationship quality and satisfaction. Literature has demonstrated moderate relationships between PTSD and suicidal ideation. A previous study conducted by two of the investigators in this population showed that perceived feelings of burdensomeness and belongingness and identification of suicide as a potential strategy for dealing with these feelings. Joiner has hypothesized that acquired capacity of painful experiences, perceived burdensomeness and thwarted belongingness are the three components of increased suicide risk. Yet few studies exist that examine these constructs in the military population, though research indicates the clinical utility for exploring these constructs and related consequences.


Recruitment information / eligibility

Status Completed
Enrollment 69
Est. completion date July 2016
Est. primary completion date December 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- OEF/OIF Veteran (at least one OEF/OIF deployment)

- Currently receiving or eligible to receive health care services at DVAMC

- In a current, established relationship for a duration of at least one year

- Age of 18-50

Exclusion Criteria:

- Inability to provide informed consent.

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

- Do not meet the inclusion criteria listed above.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Eastern Colorado Healthcare System Denver Colorado

Sponsors (1)

Lead Sponsor Collaborator
VA Eastern Colorado Health Care System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Relationship satisfaction Four item relationship satisfaction survey One study visit
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