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Family Involvement in Treatment for PTSD

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
VA Office of Research and Development
ClinicalTrials.gov Identifier:
NCT00893152
First received: May 1, 2009
Last updated: March 24, 2015
Last verified: March 2015
Results First Received: February 17, 2015  
Study Type: Observational
Condition: Posttraumatic Stress Disorder

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups
  Description
Veterans Participants in focus groups or individual qualitative interviews
Family Members Family members of participating veterans who also took part in a focus group or individual qualitative interview

Participant Flow:   Overall Study
    Veterans   Family Members
STARTED   47   36 
COMPLETED   47   36 
NOT COMPLETED   0   0 



  Baseline Characteristics
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Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
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Reporting Groups
  Description
Veterans Participants in focus groups or individual qualitative interviews
Family Members Family members of participating veterans who also took part in a focus group or individual qualitative interview
Total Total of all reporting groups

Baseline Measures
   Veterans   Family Members   Total 
Overall Participants Analyzed 
[Units: Participants]
 47   36   83 
Age 
[Units: Years]
Mean (Standard Deviation)
 37.3  (10.9)   39.1  (13.1)   38.2  (11.7) 
Gender 
[Units: Participants]
     
Female   16   27   43 
Male   31   9   40 
Region of Enrollment 
[Units: Participants]
     
United States   47   36   83 


  Outcome Measures

1.  Primary:   Qualitative Interviews - Perspectives on Family Involvement in PTSD Treatment   [ Time Frame: During the 1-1.5 hour interviews ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats
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Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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  More Information
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Certain Agreements:  
All Principal Investigators ARE employed by the organization sponsoring the study.


Results Point of Contact:  
Name/Title: Ellen P. Fischer, PhD
Organization: VA HSR&D Center for Mental Healthcare & Outcomes Research
phone: 501-257-1711
e-mail: Ellen.Fischer@va.gov



Responsible Party: VA Office of Research and Development
ClinicalTrials.gov Identifier: NCT00893152     History of Changes
Other Study ID Numbers: DHI 08-097
CAVHS 0156_2008I ( Other Identifier: CAVHS IRB )
Study First Received: May 1, 2009
Results First Received: February 17, 2015
Last Updated: March 24, 2015
Health Authority: United States: Federal Government