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WithdrawnNCT01626313FOCUSUpdated Nov 3, 2022

UCLA FOCUS Family Resiliency Training Research Study

An interventional study of FOCUS Individualized Family Resiliency Training in Veteran Families, Family Communications and Civilian Life Reintegration, sponsored by University of California, Los Angeles. Withdrawn at 1 site in United States. Open to participants aged 5 Years and older. Per ClinicalTrials.gov, last updated 2022-11-03.

Sponsored by University of California, Los Angeles · Not applicable, Interventional, and Supportive care

Why this study was withdrawn
Proposed studies were not funded
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
5 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Veteran Families
  • Family Communications
  • Civilian Life Reintegration

Keywords

  • Veteran families
  • OEF
  • OIF
  • OND
  • Resiliency
  • Psycho educational training
  • Stress
  • Military
03

In context

Lead sponsor

University of California, Los Angeles is the lead sponsor of 1,142 studies on the registry; 192 are open to participants now.

Of its 91 completed or terminated interventional studies of FDA-regulated products, 66 (73%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

Exclusion Criteria:

  • active case with Child Protective Services
  • conditions or substance use that limits ability to fully participate in the research program
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Active comparator
    Immediate intervention

    Subjects are randomized to receive immediate intervention of the 8 session FOCUS IFRT

    Behavioral: FOCUS Individualized Family Resiliency Training

  • 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

Interventions

  • BehavioralFOCUS Individualized Family Resiliency Training

    Eight session psycho educational training for families to enhance communication and reduce stressors related to return to post-military life.

06

What researchers measure

Primary outcomes

  1. Improvement on standardized behavioral health assessment scales

    Time frame: 4-6 months

07

Study locations

1 site
  • UCLA Semel Institute
    Los Angeles, California 90095, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01626313
Lead sponsor
University of California, Los Angeles
Collaborators
VA Greater Los Angeles Healthcare System
Responsible party
Shirley Glynn (Associate Researcher, University of California, Los Angeles) — Principal investigator
First posted
Jun 22, 2012
Start date
Dec 2011 (estimated)
Primary completion
Nov 2013 (estimated)
Completion
Nov 2013 (estimated)
Last update
Nov 3, 2022

Study contacts

Patricia E Lester, MD
principal investigator · University of California, Los Angeles

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Oct 2022. You cannot join it, but the record below documents what was studied.

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