Trial record 2 of 561 for:    Open Studies | "Family"

UCLA FOCUS Family Resiliency Training Research Study

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2012 by University of California, Los Angeles.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
VA Greater Los Angeles Healthcare System
Information provided by (Responsible Party):
Shirley Glynn, University of California, Los Angeles
ClinicalTrials.gov Identifier:
NCT01626313
First received: June 20, 2012
Last updated: NA
Last verified: June 2012
History: No changes posted
  Purpose

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.


Condition Intervention
Veteran Families
Family Communications
Civilian Life Reintegration
Behavioral: FOCUS Individualized Family Resiliency Training

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Masking: Open Label
Primary Purpose: Supportive Care
Official Title: UCLA FOCUS (Families OverComing Under Stress) Family Resiliency Training Research Study

Further study details as provided by University of California, Los Angeles:

Primary Outcome Measures:
  • Improvement on standardized behavioral health assessment scales [ Time Frame: 4-6 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 24
Study Start Date: December 2011
Estimated Study Completion Date: November 2013
Estimated Primary Completion Date: November 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Immediate intervention
Subjects are randomized to receive immediate intervention of the 8 session FOCUS IFRT
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.
Active Comparator: Waitlisted
Subjects are randomized to be waitlisted for 4 months, re-assessed and then receive intervention of the 8 session FOCUS IFRT
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.

  Eligibility

Ages Eligible for Study:   5 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01626313

Contacts
Contact: Lina Berrio, MPH 310-702-3991 welcomebackveteransUCLA@gmail.com
Contact: Alex Lee, MSW 855-231-9500 welcomebackveteransUCLA@gmail.com

Locations
United States, California
UCLA Semel Institute Recruiting
Los Angles, California, United States, 90095
Contact: Lina Berrio, MPH    310-702-3991    welcomebackveteransUCLA@gmail.com   
Contact: Alex Lee, MSW    855-231-9500    welcomebackveteransUCLA@gmail.com   
Principal Investigator: Patricia E Lester, MD         
Sponsors and Collaborators
University of California, Los Angeles
VA Greater Los Angeles Healthcare System
Investigators
Principal Investigator: Patricia E Lester, MD University of California, Los Angeles
  More Information

No publications provided

Responsible Party: Shirley Glynn, Associate Researcher, University of California, Los Angeles
ClinicalTrials.gov Identifier: NCT01626313     History of Changes
Other Study ID Numbers: 11-003001
Study First Received: June 20, 2012
Last Updated: June 20, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, Los Angeles:
Veteran families
OEF
OIF
OND
Resiliency
Psycho educational training
Stress
Military

ClinicalTrials.gov processed this record on September 18, 2014