NCT06963554 Examining Whether Project Support Works
| NCT ID | NCT06963554 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Medical University of South Carolina |
| Condition | Parent-Child Relations |
| Study Type | INTERVENTIONAL |
| Enrollment | 100 participants |
| Start Date | 2025-11-04 |
| Primary Completion | 2027-11-01 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 100 participants in total. It began in 2025-11-04 with a primary completion date of 2027-11-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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
Inclusion Criteria: * 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; * Child has been living with caregiver for the last 6 months or longer; * Family is able to participate in services delivered via telehealth. Exclusion Criteria: * 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.
Contact & Investigator
Caitlin Rancher, PhD
PRINCIPAL INVESTIGATOR
Medical University of South Carolina
Frequently Asked Questions
Who can join the NCT06963554 clinical trial?
This trial is open to participants of all sexes, aged 6 Years or older, up to 13 Years, studying Parent-Child Relations. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06963554 currently recruiting?
Yes, NCT06963554 is actively recruiting participants. Contact the research team at rancher@musc.edu for enrollment information.
Where is the NCT06963554 trial being conducted?
This trial is being conducted at Charleston, United States.
Who is sponsoring the NCT06963554 clinical trial?
NCT06963554 is sponsored by Medical University of South Carolina. The principal investigator is Caitlin Rancher, PhD at Medical University of South Carolina. The trial plans to enroll 100 participants.