Burden, Belonging, and Response to Pain in Veterans
|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.|
|ClinicalTrials.gov Identifier: NCT01507675|
Recruitment Status : Withdrawn (Study should not have been listed on ClinicalTrials)
First Posted : January 11, 2012
Last Update Posted : March 26, 2014
|Condition or disease|
Show Detailed Description
|Study Type :||Observational|
|Actual Enrollment :||0 participants|
|Observational Model:||Ecologic or Community|
|Official Title:||Burden, Belonging, and Response to Pain in Veterans|
|Study Start Date :||October 2011|
|Estimated Primary Completion Date :||April 2014|
|Estimated Study Completion Date :||April 2014|
Participants will be recruited from the Denver VA Medical Center (DVAMC), regardless of clinic.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
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): NCT01507675
|United States, Colorado|
|Va Visn 19 Mirecc|
|Denver, Colorado, United States, 80220|
|Principal Investigator:||Peter M. Gutierrez, PhD||Clinical Research Psychologist VA VISN 19 MIRECC|