A Single-session Intervention Adaptation of the Habit Framework for the Prevention of Eating Disorders (NCT06861608)

🧪 Interventions in This Study

• Screening Questionnaire (BEHAVIORAL)
• Pre-Intervention Questionnaires (~10 minutes) (BEHAVIORAL)
• SSI (Single-session intervention (~30 minutes) Active arm (BEHAVIORAL)
• SSI (Single-session intervention (~30 minutes) control arm (BEHAVIORAL)
• End-of-Intervention Questionnaires (~5 minutes) (BEHAVIORAL)

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (1 Sites)

• Virginia Commonwealth University — Richmond, Virginia

📞 Contact the Study Coordinator

Phone: (518) 376-2543

Email: breinerc@vcu.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 Eating Disorder Not Otherwise Specified clinical trials

💡 How to Participate

1. Check the checklist above to see if you may qualify.
2. Contact the study coordinator using the phone/email above.
3. Ask about the visit schedule, what is covered at no cost, and any travel support.
4. Confirm with your own doctor before making a decision.