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RecruitingNCT07209488AMTUpdated May 6, 2026

Acquired Dyslexia Modeling and Treatment

An interventional study of Phono-Motor Therapy and Semantic Feature Analysis in Stroke and Dyslexia, Acquired, sponsored by Rutgers, The State University of New Jersey. Recruiting at 3 sites in United States. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2026-05-06.

Sponsored by Rutgers, The State University of New Jersey · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Dec 2025; still recruiting 10 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Non-randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Stroke
  • Dyslexia, Acquired

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Keywords

  • reading
  • computational model
  • treatment
  • therapy
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's planned enrollment of 12 is below the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Rutgers, The State University of New Jersey is the lead sponsor of 496 studies on the registry; 130 are open to participants now.

Of its 38 completed or terminated interventional studies of FDA-regulated products, 30 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Fluent in English as a first language pre-stroke by self report.
  • Normal or corrected-to-normal vision.
  • Normal or aided hearing.
  • Left hemisphere ischemic or hemorrhagic stroke (as verified by a structural brain scan).
  • Impaired reading as confirmed by significant impairment in the Basic Skills cluster of the Woodcock Reading Mastery Test - III.

Exclusion criteria

Exclusion Criteria:

  • Diagnosed pre-stroke neurological disease affecting the brain other than left hemisphere stroke.
  • Severe apraxia of speech (determined by consensus judgment among speech-language pathologists).
  • History of learning disabilities such as developmental dyslexia or current self-reported major psychiatric disorders.
  • Inability to undergo, or provide a copy of, a post-stroke brain imaging scan.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Crossover assignment
Masking
Single (Participant)
Enrollment
12 participants (estimated)

Study arms

  • Experimental
    Model-matched

    This group will receive the therapy, either phonological or semantics-based, that matches the computational model prediction for the source of their reading impairment. They will receive this for the first 60 total hours of therapy, and for the second 60 hours of therapy.

    Behavioral: Phono-Motor Therapy · Behavioral: Semantic Feature Analysis

  • Active comparator
    Model-non-matched

    This group will receive the therapy, either phonological or semantics-based, that does not match the computational model prediction for the source of their reading impairment. They will receive this for the first 60 total hours of therapy. For the second 60 hours, they will receive the other therapy.

    Behavioral: Phono-Motor Therapy · Behavioral: Semantic Feature Analysis

Interventions

  • BehavioralPhono-Motor Therapy

    Orthographic stimuli (letters) are introduced from the beginning as each phoneme is being trained. This maintains the focus on phonology, while emphasizing its relevance to reading. PMT consists of an initial phase focused on training of individual phonemes and phoneme sequences in spoken language, followed by written language tasks. English phonemes are first trained in isolation, followed by phoneme sequences in words and pseudowords. They are trained multi-modally through emphasis on auditory, motor, tactile-kinesthetic, visual, and orthographic representations for each consonant and vowel. When sequences are introduced, focus on phonology is maintained by training on pseudowords first before real words are introduced. Participants work on identifying, repeating, parsing, blending, and manipulating phonemes that make up the pseudoword and word stimuli. To maintain focus on phonology, pictures and definitions of the stimuli are never shown or discussed.

    Also known as: PMT

  • BehavioralSemantic Feature Analysis

    SFA activates semantic features of the target word to help retrieve the spoken form of the word. To target reading, a modified SFA is used with written words rather than pictures as the primary materials. Pictures are instead included for each word as a semantic feature. Stimuli will consist of 80 highly imageable nouns with a range of word frequencies. During treatment the therapist will present a written noun and ask the participant a series of questions about the features of that noun. For example, if the presented noun is "juice", the therapist would have the participant select the corresponding picture from an array of pictures. The therapist then would ask, "what do you do with it?" (eliciting a feature from the "function" category) and "where do you store it in your home?" (eliciting a feature from the "context" category). This is done for a total of 6 categories of semantic features. The process is repeated until the participant reads the noun correctly three times in a row.

    Also known as: SFA

06

What researchers measure

Primary outcomes

  1. Woodcock Reading Mastery Test - III

    The WRMT-III is a standardized measure of reading skills.

    Time frame: Baseline, following the first 60 hours of therapy, and following the final 60 hours of therapy.

  2. Test words and pseudowords

    Change in accuracy of reading 120 test words and 80 pseudowords

    Time frame: Baseline, following the first 60 hours of therapy, and following the final 60 hours of therapy.

Secondary outcomes

  1. Western Aphasia Battery - Revised

    The WAB - R is a standard measure of aphasia severity. It determines both the degree of aphasia and whether treatment has any impact on aspects of aphasia other than acquired dyslexia.

    Time frame: Baseline, following the first 60 hours of therapy, and following the final 60 hours of therapy.

  2. Comprehensive Aphasia Test - Disability Quotient

    The CAT - DQ is a self-report measure of subjectively perceived degree of disability.

    Time frame: Baseline, following the first 60 hours of therapy, and following the final 60 hours of therapy.

07

Study locations

3 of 3 sites recruiting
  • Florida State University
    Tallahassee, Florida 32306, United States
    Recruiting
  • Johns Hopkins University School of Medicine
    Baltimore, Maryland 21287, United States
    Recruiting
  • Kessler Foundation
    West Orange, New Jersey 07052, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Pursuant to the rules of the Institutional Review Board of Rutgers, The State University of New Jersey, only data that can be fully de-identified will be shared. All data collected using non-proprietary (non-copyrighted) instruments are expected to be de-identifiable and therefore will be shared in de-identified form. These include: structural brain images (de-faced), results of the test for hemi-spatial neglect, the experimental list of 120 words and 80 pseudowords for reading aloud, and results of touch-screen choice tasks for testing phonological, semantic, and orthographic knowledge.

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07209488
Lead sponsor
Rutgers, The State University of New Jersey
Collaborators
National Institute on Deafness and Other Communication Disorders (NIDCD)
Responsible party
William W. Graves, Ph.D. (Associate Professor, Rutgers, The State University of New Jersey) — Principal investigator
First posted
Oct 7, 2025
Start date
Dec 3, 2025
Primary completion
Sep 2026 (estimated)
Completion
Sep 2026 (estimated)
Last update
May 6, 2026

Study contacts

William W Graves, PhD
Contact
william.graves@rutgers.edu
973-353-3947
Olga Boukrina, PhD
Contact
OBoukrina@KesslerFoundation.org
973-324-3587
William W Graves, PhD
principal investigator · Rutgers, The State University of New Jersey

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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