- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00125242
Word-Retrieval Treatment for Aphasia: Semantic Feature Analysis
Word-Retrieval for Aphasia: Facilitation of Generalization
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The purpose of the proposed research is to examine the effects of a semantically-oriented treatment on word retrieval in persons with aphasia. The planned investigations are designed to further the development of semantic feature training so that it may serve as not only a mechanism for improving disrupted lexical semantic processing, but also as a compensatory strategy during word retrieval failures. The proposed research will also address the issue of exemplar typicality (Kiran & Thompson, 2003) by examining the effects of training typical versus atypical exemplars of various categories with individuals with different types of aphasia. A series of 24 single subject experimental designs will be conducted in the context of a group design to address the following experimental questions:
- Will training atypical examples of living and artifact noun categories using semantic feature training result in a significantly different outcome* than training typical examples of living and artifact noun categories?
- Will training of one category of nouns using semantic feature training result in improved retrieval of untrained categories of nouns?
- Will effects of semantic feature training vary across aphasia types?
- Will semantic feature training result in increased production of content during discourse?
Will generalization to untrained typical examples vary across generalization lists that are repeatedly exposed and those that are limited in exposure? (i.e., Does repeated exposure appear to contribute to generalization?)
- Outcome measure will reflect acquisition, response generalization within category, and response generalization across category effects of treatment.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Utah
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Salt Lake City, Utah, United States, 84148
- VA Salt Lake City Health Care System, Salt Lake City
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Diagnosis of Wernicke's, Broca's, or Conduction aphasia with significant word-retrieval deficits
- At least 6 months post-onset of single, left-hemisphere stroke
- Minimum of high-school education
- Visual and auditory acuity sufficient for experimental tasks
- Nonverbal intelligence within normal limits
Exclusion Criteria:
- Diagnosed mental illness other than depression
- Neurological condition other than that which resulted in aphasia
- History of alcohol or substance abuse
- Non-native English speaker
- Premorbid history of speech/language disorder
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Semantic Feature Analysis (SFA)
Word retrieval treatment for aphasia.
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SFA entails having the speech-language pathologist (SLP) guide the participant through generation of pertinent semantic features for pictured treatment items (e.g., category membership, physical description, location of item in context, personal associations, action associated with item).
For some participants, treatment items were grouped according to typicality of category membership (e.g,, a robin-typical bird and penguin-atypical bird).
Training of atypical items may stimulate a broader semantic activation of the category and thus, may promote greater generalization.
Treatment was applied sequentially to sets of items in the context of single-subject, multiple baseline designs.
In this way, replication of treatment effects could be evaluated within and across participants.
Treatment was administered by certified SLPs three times per week until prescribed accuracy levels were met during nontreatment probes or a maximum number of treatment sessions was completed.
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No Intervention: Participants for Stimuli Development
Non-brain-injured participants provided data for development of treatment stimuli.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Word Retrieval Accuracy
Time Frame: End of treatment and at 6 weeks post treatment
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Accuracy of naming of pictured treated and untreated items was assessed in probes conducted separate from treatment.
Probes were conducted repeatedly throughout the study, from baseline (prior to treatment) to follow-up (6 weeks following treatment).
All naming responses were scored using a 0-10 scale reflecting promptness and presence of errors; scores of 8-10 received an "accuate" score and scores of 0-7 received an "inaccurate" score.
A percentage accuracy score was calculated for each experimental set of items for every probe session.
Baseline probe scores were compared to end of treatment and follow-up probe scores to obtain individual effect sizes for each experimental list of items for each participant (i.e., several effect sizes were calculated for each participant).
All effect sizes were utlized to obtain an average effect size for each participant; these averages were then utlized to obtain a group average.
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End of treatment and at 6 weeks post treatment
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Collaborators and Investigators
Investigators
- Principal Investigator: Julie L. Wambaugh, PhD, VA Salt Lake City Health Care System, Salt Lake City
Publications and helpful links
General Publications
- Wambaugh JL, Mauszycki S, Cameron R, Wright S, Nessler C. Semantic feature analysis: incorporating typicality treatment and mediating strategy training to promote generalization. Am J Speech Lang Pathol. 2013 May;22(2):S334-69. doi: 10.1044/1058-0360(2013/12-0070).
- Wambaugh JL, Mauszycki S, Wright S. Semantic feature analysis: Application to confrontation naming of actions in aphasia. Aphasiology. 2013 Oct 28; 28(1):DOI:10.1080/02687038.2013.845739.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
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
- C3826-R
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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