Multiphase Optimization Strategy (MOST) for Treating Pediatric Post-traumatic Stress Disorder (PTSD) (NCT06956781)
Optimizing Behavioral Health Services Following Pediatric Trauma Exposure
🩺 Plain-English Summary (8th-Grade Level)
The goal of this clinical trial is to test the extent to which different treatment components work to improve pediatric post-traumatic stress disorder (PTSD). It will also provide evidence for how these components work. The main research questions are: What are the effects of different components used to treat PTSD? What do these components change to produce benefits in PTSD? Researchers will: Compare components to a psychological placebo to estimate their effects and measure how they work Examine how components work alone and in conjunction with other components Participants will: Receive different combinations of components and placebo Attend weekly treatment sessions Provide information to evaluate changes in PTSD
Who can join: Review the eligibility criteria below.
Location: The Mt. Hope Family Center — Rochester, New York
Age range: 8 Years to 17 Years
🧪 Interventions in This Study
- Emotion Regulation (BEHAVIORAL)
- Exposure (BEHAVIORAL)
- Cognitive Processing (BEHAVIORAL)
- Bi-lateral Stimulation (BEHAVIORAL)
- Psychological Placebo (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- The Mt. Hope Family Center — Rochester, New York
📞 Contact the Study Coordinator
Phone: (585) 275-8704
Email: chad.shenk@rochester.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.
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💡 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.