Family coping resources intervention for PTSD
Strengthening Family Coping Resources Open Trials
University of Maryland, Baltimore · NCT01754610
This study tests a program that helps families affected by trauma learn better coping skills to see if it can reduce PTSD symptoms in both kids and their parents.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 1 Year to 17 Years |
| Sex | All |
| Sponsor | University of Maryland, Baltimore (other) |
| Locations | 1 site (Baltimore, Maryland) |
| Trial ID | NCT01754610 on ClinicalTrials.gov |
What this trial studies
The Strengthening Families Coping Resources (SFCR) intervention focuses on families affected by trauma, aiming to enhance coping skills and reduce PTSD symptoms in both children and adult caregivers. This observational study evaluates the effectiveness of a manualized, skills-based treatment delivered in a multi-family group format. Families will participate in sessions designed to improve communication, emotional regulation, and overall family functioning while addressing trauma-related issues. The study will assess changes in family dynamics, coping resources, and symptom reduction through pre- and post-evaluations.
Who should consider this trial
Good fit: Ideal candidates include children aged 1 to 17 years who have experienced multiple traumas and have a partial diagnosis of PTSD, along with their caregivers.
Not a fit: Patients with active suicidal ideation, severe mental health issues, or unstable living conditions may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the mental health and coping abilities of families dealing with trauma.
How similar studies have performed: Previous studies have shown promise in using family-based interventions for trauma, suggesting that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Children aged 1 through 17 years old at the time of recruitment * Child and family exposed to multiple traumas * a partial diagnosis of PTSD (15-week treatment version) * currently in the custody of a caregiver who agrees to participate in the study. * a stable caregiving system as defined by a recent history of stability and unlikely to change in the next 6 months. Exclusion Criteria: * Children will be excluded only if they have active suicide ideation, an imminent risk for re-exposure due to their living environment, active psychosis, severe mental retardation or brain injury * Parent/caregiver has active psychosis or is a danger to self/others.
Where this trial is running
Baltimore, Maryland
- University of Maryland, School of Medicine, Department of Psychiatry, Divsion of Services Research — Baltimore, Maryland, United States (RECRUITING)
Study contacts
- Principal investigator: Laurel J Kiser, Ph.D. — University of Maryland, Baltimore
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Intervention Effectiveness, Practice-based Evidence, Posttraumatic Stress Disorder, family trauma, multi-family therapy, poverty