Who is eligible for clinical trial NCT06827951?

Participants must meet the protocol's inclusion criteria for Autonomic Dysregulation. The stated age range is 18 Years to 89 Years. Confirm all requirements with the study coordinator.

Does clinical trial NCT06827951 provide travel or cost reimbursement?

Check with the site coordinator at the participating facility for travel and lodging stipend availability, and for which routine-care costs are covered.

🏛️ Verified NIH Record • Updated 2026-02-09

Potential Benefits of Parent Child Interaction Therapy (PCIT) (NCT06827951)

A Mixed-Methods Approach Utilizing Self-Report Scales and Oxytocin Levels to Determine the Potential Benefits of Parent Child Interaction Therapy (PCIT)

🟢 Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: University of Florida

🩺 Plain-English Summary (8th-Grade Level)

The goal of this study is to explore possible benefits of Parent-Child Interaction Therapy (PCIT). The main goals of the study are: * To investigate whether pre-survey measures of autonomic reactivity relate to the overall functioning of participants. * To examine the effects of PCIT To identify individual characteristics that influence the effects of PCIT. Participants will: * complete 5 online surveys (1x pre-PCIT, 3x during PCIT, and 1x post-PCIT) * complete the PCIT program

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (4 items) and avoid the listed exclusions (4 items).

Location: UF Health Child Psychiatry — Gainesville, Florida

Age range: 18 Years to 89 Years

🧪 Interventions in This Study

Parent-Child Interaction Therapy (PCIT) (BEHAVIORAL)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Parents of children aged 2-7 years old who are eligible for Parent-Child Interaction Therapy (PCIT) based on behavioral concerns.
The primary caregiver of the child and be actively involved in the child's daily care.
Willing to attend all PCIT sessions and complete pre-, mid- and post-intervention assessments.
Fluent in English to ensure comprehension of the intervention and assessment materials.

Usually NOT eligible if any of the following apply:

Exclusion Criteria:
Parents with diagnosed severe mental health disorders (e.g., schizophrenia, bipolar disorder) that may interfere with participation in PCIT.
Children with conditions that require interventions other than PCIT (e.g., severe developmental disabilities).
Parents who have previously participated in PCIT are excluded to avoid confounding results.

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (2 Sites)

UF Health Child Psychiatry — Gainesville, Florida
UF Health Psychiatry San Jose — Jacksonville, Florida

📞 Contact the Study Coordinator

Phone: (904) 383-1038

Email: Britney.Duner@jax.ufl.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 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 § 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.

Explore by condition: All Autonomic Dysregulation clinical trials

💡 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.

🏛️ View Official NIH Record ↗