Building Resilient Families (NCT05388864)
A Multi-Component Intervention to Strengthen Families With Adverse Childhood Experiences (ACEs)
๐ฉบ Plain-English Summary (8th-Grade Level)
Prior research suggests that it is possible to improve health outcomes in children with ACEs through multi-component interventions. The challenge for most communities is that health and education systems are fragmented and fail to accommodate families based upon different levels of need. This study utilizes cross-sectoral partnerships to mobilize three vectors (pediatricians, community health workers and parenting educators) to optimize the delivery of vital information and resources to a diverse population of families with ACEs. All vectors are trained in an evidence-informed curriculum to strengthen families and build youth resilience. The study design is a randomized controlled trial of 340 families of children between the ages of 3 to 11 who are generally healthy and have recently seen a pediatrician for a well-child visit. To evaluate the efficacy of this intervention, pediatric patients are invited to participate in repeat evaluations within 2 weeks, 3 months, 6 months, and 12 months after their well-child visit. The study will evaluate the following: 1) the association between Child-ACE scores and biomarkers of toxic stress at baseline in children age 3-11 years old; 2) whether the intervention reduces toxic stress and child health and psychosocial problems at follow-up for children with ACEs compared to usual well-child care for children with ACEs; and 3) the impact of mediating and moderating variables. These results will demonstrate that for families with ACEs the intervention will decrease toxic stress associated with ACEs, improve health outcomes, and reduce health disparities.
Who can join: Review the eligibility criteria below.
Location: Loma Linda University โ Loma Linda, California
Age range: 3 Years to 11 Years
๐งช Interventions in This Study
- Three-Tier Model (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- Loma Linda University โ Loma Linda, California
๐ Contact the Study Coordinator
Phone: (909) 651-5672
Email: amariemitchell@llu.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Adverse Childhood Experiences
- Playing Playfully to Overcome Adversity โ Fairfield, Connecticut
- The THRIVE Study: Teaching Healthy Regulation in Individuals & Vulnerable Environments โ Irvine, California
- Childhood Trauma, Exercise, and Cognition โ Austin, Texas
- ACEs, SIRT1, and Premature Vascular Aging in Humans โ Iowa City, Iowa
- Neurobehavioral Mechanisms Linking Childhood Adversity to Increased Risk for Smoking โ Durham, North Carolina
Explore by condition: All Adverse Childhood Experiences clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.