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FOCUS-CI: A Preventive Intervention With Children and Families of the Combat Injured

H

Henry M. Jackson Foundation for the Advancement of Military Medicine

Status

Terminated

Conditions

Traumatic Stress Disorders
Combat Disorders
Stress Disorders

Treatments

Behavioral: FOCUS-CI
Behavioral: Standard of Care

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT01062022
W81XWH-08-2-0650 (Other Grant/Funding Number)
G188NI

Details and patient eligibility

About

The purpose of this study is to implement a unique evidence-based intervention program to help military families deal with the critical issue of combat injury and its impact on current and future family health and functioning. The study is a randomized study. The study will compare the effects of the newly designed FOCUS-CI (Families OverComing Under Stress - Combat Injury) with the existing standard of care (SoC) at three military medical rehabilitation sites (Walter Reed Amry Medical Center, Brooke Army Medical Center and Madigan Army Medical Center) on key aspects of family health and functioning.

Full description

Injured service members who have at least one child between the ages of 5 and 18 years who have sustained a combat injury severe enough to require at least two weeks of inpatient hospitalization and who are within 6 months of discharge from inpatient hospitalization and currently receiving outpatient care will be recruited into this study.

Enrollment

23 patients

Sex

All

Ages

5+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

For a family to be eligible for the study, the injured service member must:

  • have sustained a combat injury that was severe enough to require a minimum of two weeks inpatient hospitalization immediately after the injury;
  • currently be participating in outpatient rehabilitation for the same combat injury;
  • must be within 6 months of discharge from inpatient hospitalization at the start of the intervention;
  • families must have at least one child between the ages of 5 and 18 and be fluent in English. English fluency will be determined by asking, "Is English spoken in your home?"
  • pregnant women are eligible to participate.

Exclusion criteria

  • families in which the service member did not sustain a qualifying injury or has been discharged from inpatient care for more than six months will not be eligible to participate
  • families in which a member is actively psychotic
  • families in which a service member's primary relationship is with a "significant other" who is not eligible for military medical care
  • due to the limited ability of young children to comprehend the intervention activities, children under the age of 5 years will not be invited to participate in the intervention.
  • no one will be excluded based on race, ethnicity, gender, pregnancy, medical status, or cognitive functioning.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

23 participants in 2 patient groups

Control - Standard of Care
Active Comparator group
Description:
Participation in the study will involve your child completing a questionnaire about (a) your family's background, descriptive information about people in your family, and previous major life events, (b) his/her current functioning, (c) his/her feelings before, during, and after the combat injury, and (d) his/her current social relationships and adjustment. Your child will be asked to complete the questionnaire during the baseline assessment, and at 6 months, 12 months, and 24 months after the original assessment.
Treatment:
Behavioral: Standard of Care
FOCUS-CI
Active Comparator group
Description:
Those participants in the FOCUS-CI intervention will be part of a family skill-building/resiliency training program designed to provide information and skills training in a variety of forms, including clinician-led sessions, handouts, on-line training modules, and individual family care management. Study participation will also involve completing a questionnaire about (a) your family's background, descriptive information about people in your family, and previous major life events, (b) his/her current functioning, (c) his/her feelings before, during, and after the combat injury, and (d) his/her current social relationships and adjustment. Questionnaires will be completed during the baseline assessment, and at 6 months, 12 months, and 24 months after the baseline assessment.
Treatment:
Behavioral: FOCUS-CI

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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