Burden, Belonging, and Response to Pain in Veterans
Study Overview
Status
Status
Conditions
Conditions
Detailed Description
Study Type
Study Type
Contacts and Locations
Study Locations
-
-
Colorado
-
Denver, Colorado, United States, 80220
- VA VISN 19 MIRECC
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Military veteran
- 18 or older
- Ability to respond to questions regarding the informed consent
Exclusion Criteria:
- Active-duty military
- Non-English speaking
- Inability to respond to questions regarding the informed consent procedure
Study Plan
How is the study designed?
Design Details
Number of groups / cohorts
Cohorts and Interventions
Group / CohortGroup / Cohort |
|---|
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Military Veterans
Participants will be recruited from the Denver VA Medical Center (DVAMC), regardless of clinic.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Internal consistency reliability.
Time Frame: two years
|
The internal consistency reliability statistics will be calculated for all study variables to confirm the measures are reliable.
|
two years
|
|
Convergent validity.
Time Frame: two years
|
Convergent validity of the Interpersonal Needs Questionnaire (INQ) will be determined by examining the correlation between it and the other study measures.
|
two years
|
|
Convergent validity.
Time Frame: two years
|
Convergent validity of the acquired capability of suicide scale (ACSS) will be determined by correlating it with all other measures.
|
two years
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Discriminant validity.
Time Frame: two years
|
Discriminant validity of the interpersonal needs questionnaire (INQ) will be determined by examining correlations with measures of unrelated constructs.
|
two years
|
|
Suicide risk.
Time Frame: two years
|
Examine the effects of scores on the SLP on the relationship between reasons that people have for living and the potential for engaging in at-risk behavior.
|
two years
|
|
Discriminant validity
Time Frame: two years
|
Examine the discriminant validity of the acquired capability for suicide scale (ACSS) by examining correlations between it and measures of unrelated constructs.
|
two years
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Peter M. Gutierrez, PhD, Clinical Research Psychologist VA VISN 19 MIRECC
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (ANTICIPATED)
Primary Completion
Study Completion (ANTICIPATED)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
First Posted
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- COMIRB 11-0948
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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