- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06619756
Anomia Treatment Predictors
November 7, 2025 updated by: Nichol Castro, State University of New York at Buffalo
Predictors of Phonological-focused Anomia Treatment
The goal of this clinical trial is to identify predictors of response to phonological-focused anomia treatment in people with aphasia.
The main question it aims to answer is who responds to which type of anomia treatment.
Researchers will compare Phonomotor Treatment and Phonological Components Analysis to see which treatment is more beneficial, and for whom.
Participants will engage in both treatments over several months.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Participants will complete screening and characterization testing to determine eligibility for the study.
Each treatment will be administered twice a week, for 10-15 sessions.
Pre-treatment and post-treatment testing will also occur for each treatment.
There will be a period of no treatment in between the first and second treatment blocks.
Study Type
Interventional
Enrollment (Actual)
2
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
Buffalo, New York, United States, 14214
- UB Audiology and Speech-Language Pathology Clinic
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Chronic aphasia (6+ months)
- Anomia
- Sufficient auditory comprehension to follow task instructions
- Phonologic impairment
Exclusion Criteria:
- Progressive neurological illness or disease, including dementia
- Chronic medical illness that interferes with adherence to testing schedule
- Severe, uncorrected vision or hearing impairment that interferes with task completion
- Moderate-severe apraxia of speech or dysarthria that interferes with task completion
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PMT
Phonomotor Treatment (PMT) will be administered.
This treatment improves anomia by training the sound sequences of words.
This is a multimodal treatment approach that includes listening, producing, visualizing, and describing sounds and sound sequences.
The participant practices the sound sequence tasks with the clinician.
|
Anomia treatment focuses on improving word-finding abilities.
This intervention targets the phonology of words to improve word-finding.
|
|
Experimental: PCA
Phonological Components Analysis (PCA) will be administered.
This treatment improves anomia by identifying phonological features of words.
A picture is presented.
The participant provides features of the picture name: the first sound of the word, the final sound of the word, the number of syllables of the word, another word that starts with the same sound, and another words that rhymes with the word.
The participant attempts to produce the word independently and by repeating after the clinician.
|
Anomia treatment focuses on improving word-finding abilities.
This intervention targets the phonology of words to improve word-finding.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Naming of Trained Words
Time Frame: Pre-treatment and Immediately post-treatment
|
Picture naming of trained words
|
Pre-treatment and Immediately post-treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Naming of Untrained Words
Time Frame: Pre-treatment and Immediately post-treatment
|
Picture naming of untrained words
|
Pre-treatment and Immediately post-treatment
|
|
Standardized Assessment of Phonology in Aphasia (SAPA)
Time Frame: Pre-treatment and Immediately post-treatment
|
The SAPA assesses phonological processing abilities, including oral reading, rhyme judgments, minimal pair judgments, lexical decision, blending, and parsing.
|
Pre-treatment and Immediately post-treatment
|
|
Philadelphia Naming Test
Time Frame: Pre-treatment and Immediately post-treatment
|
The short-form of the Philadelphia Naming Test is a picture naming test of items not seen during treatment.
|
Pre-treatment and Immediately post-treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nichol Castro, PhD, SUNY at Buffalo
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 18, 2024
Primary Completion (Actual)
October 1, 2025
Study Completion (Actual)
October 1, 2025
Study Registration Dates
First Submitted
September 27, 2024
First Submitted That Met QC Criteria
September 27, 2024
First Posted (Actual)
October 1, 2024
Study Record Updates
Last Update Posted (Actual)
November 12, 2025
Last Update Submitted That Met QC Criteria
November 7, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00008623
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Sample size is low increasing risk of identification of individuals.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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