- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07179458
- Original Trial
Criterion-learning Naming Treatment For Addressing Comprehension Deficits in Aphasia
Word Retrieval in Aphasia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study examines a retrieval practice-based naming treatment termed criterion learning. In criterion learning, each item's assigned criterion level dictates the number of times that item is correctly retrieved before it is dropped from further training within a session. Criterion learning optimally incorporates potent learning experiences, including spaced retrieval practice with emphasis on correct retrievals during training. The present study will provide critical observations for optimizing criterion learning for treating word processing deficits in people with aphasia. This study will recruit 20 community-dwelling individuals with aphasia, who will undergo comprehensive neuropsychological characterization. Subsequently, participants will engage in an experimental treatment designed to promote improvements in word processing deficits.
This study will examine transfer from two types of naming treatment to word comprehension performance. Each PWA will perform naming treatment in one session at different dosages with a test of comprehension performance administered approximately one week and one month following treatment. Main outcomes of interest will be degree of transfer of each type of naming treatment to comprehension performance.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Pennsylvania
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Elkins Park, Pennsylvania, United States, 19027
- Jefferson Moss Rehabilitation Research Institute
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- English as a native or primary language
- Adults with stroke who are at least 6 months post-onset
- Exhibit semantic comprehension deficit, defined as a minimum of 80 errors on word-picture verification pre-test
Exclusion Criteria:
- History of comorbid neurological diagnoses, such as Multiple Sclerosis or Parkinson's Disease
- History of a learning disability that significantly impacted language development, such as developmental language disorder
- Insufficient stamina to participate in the protocol
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Criterion-learning practice
This is a single-arm study
|
The experiments will be presented on a computer.
On each criterion-learning trial, a picture is presented and the participant is asked to try to produce the name for the object with or without a cue.
Correct-answer feedback is provided.
Criterion learning involves presenting a block of items in fixed order, and on each trial, the experimenter or a voice-recognition component will code the response during the trial as correct/incorrect.
When the item reaches its assigned criterion level, it is dropped from further training in a session.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trained comprehension items
Time Frame: approximately one-week and one-month following treatment
|
Word-picture verification task
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approximately one-week and one-month following treatment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trained naming items
Time Frame: a single session held during a single day, scheduled at the participant's convenience but typically held within two weeks following pre-treatment assessment
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Confrontation naming task that involves trained items
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a single session held during a single day, scheduled at the participant's convenience but typically held within two weeks following pre-treatment assessment
|
|
Trained comprehension items
Time Frame: pre-treatment
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Word-picture verification task
|
pre-treatment
|
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Untrained comprehension items
Time Frame: pre-treatment, approximately one-week and one-month post-treatment
|
Word-picture verification task
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pre-treatment, approximately one-week and one-month post-treatment
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Erica L Middleton, PhD, Albert Einstein Healthcare Network
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 4526.4
- R01DC015516 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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