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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01626313
Other study ID # 11-003001
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date December 2011
Est. completion date November 2013

Study information

Verified date October 2022
Source University of California, Los Angeles
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will examine the effectiveness of an eight session, manualized individual family resiliency training (IFRT) for families with one OEF/OIF/OND veteran in promoting better family communication relating to return to post military life.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date November 2013
Est. primary completion date November 2013
Accepts healthy volunteers No
Gender All
Age group 5 Years and older
Eligibility Inclusion Criteria: - OEF/OIF/OND Veteran adult family member - cohabiting with significant other for 6 months or more - at least one child age 5 to 17 years Exclusion Criteria: - active case with Child Protective Services - conditions or substance use that limits ability to fully participate in the research program

Study Design


Intervention

Behavioral:
FOCUS Individualized Family Resiliency Training
Eight session psycho educational training for families to enhance communication and reduce stressors related to return to post-military life.

Locations

Country Name City State
United States UCLA Semel Institute Los Angeles California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Los Angeles VA Greater Los Angeles Healthcare System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement on standardized behavioral health assessment scales 4-6 months