πŸ›οΈ Verified NIH Record β€’ Updated 2026-05-05

Acquired Dyslexia Modeling and Treatment (NCT07209488)

Evidence-based Modeling for Acquired Dyslexia Treatments

🟒 Recruiting Observational / Diagnostic 🧠 Behavioral & Psychological Program Sponsor: Rutgers, The State University of New Jersey

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

This study is a low-risk, early phase 1, multicenter trial to test the use of a computational (neural network) cognitive model of reading to simulate acquired dyslexia and its treatment. The aim is to determine whether there is an advantage to receiving the treatment the model predicts to be advantageous compared to the alternative treatment. All participants will receive two full rounds of treatment. A round of treatment will consist of either phonomotor treatment (PMT) or semantic feature analysis (SFA) for 60 hours, distributed over 5 days a week for 2 hours a day.

Who can join: Review the eligibility criteria below.

Location: Florida State University β€” Tallahassee, Florida

Age range: 18 Years to 85 Years

πŸ§ͺ Interventions in This Study

  • Phono-Motor Therapy (BEHAVIORAL)
  • Semantic Feature Analysis (BEHAVIORAL)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (3 Sites)

  • Florida State University β€” Tallahassee, Florida
  • Johns Hopkins University School of Medicine β€” Baltimore, Maryland
  • Kessler Foundation β€” West Orange, New Jersey

πŸ“ž Contact the Study Coordinator

Phone: (973) 353-3947

Email: william.graves@rutgers.edu

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

πŸ’° 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 Β§ 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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πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—