About this trial
This study will involve a randomized, controlled trial with two parallel groups, Project Support and a treatment as usual control group. Families with a child on the waitlist for trauma-focused services will be invited to participate. Participation involves completing a baseline assessment of family functioning and trauma characteristics. Participants will then be randomized to either Project Support or the treatment as usual control group. All participants will be invited to complete the post-test assessment 4-6 weeks after the baseline assessment, prior to beginning trauma-focused services.
Eligibility criteria
Qualifiers
Family is seeking trauma-focused services for their child;
Child is between 6 - 13 years old;
Caregiver agreed to be contacted for volunteer research opportunities;
Caregiver and child can communicate in English or Spanish;
Disqualifiers
Child or caregiver has a diagnosis that would impair their ability to participate in or benefit from services (e.g., traumatic brain injury, developmental disability, psychosis);
Child is in Foster Care or Department of Social Services custody;
The caregiver is unwilling or unable to give informed consent and/or the child is unwilling and unable to give assent.
Trial design
Treatments tested in this trial
- Project Support
- Case Management Services
Treatment groups
Sponsors and collaborators
Medical University of South Carolina
Lead sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator