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Sentence Training for Aphasia
N/A
Recruiting
Led By Jiyeon Lee, PhD
Research Sponsored by Purdue University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Normal or corrected to normal hearing and vision
Be older than 18 years old
Must not have
Severe apraxia of speech
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from baseline up to 1-week post training or 2-month post treatment
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to improve sentence production and comprehension in people with aphasia using a technique that subtly influences the brain to enhance language skills without the person being fully aware of it. The goal is to create lasting improvements in language abilities by frequently exposing the brain to certain language patterns.
Who is the study for?
This trial is for English-speaking adults who had a stroke in the left hemisphere of their brain at least 6 months ago, causing aphasia. They should have completed high school and have normal or corrected vision and hearing. Participants must struggle with forming sentences but can use some words independently. Those with uncontrolled mental health issues, substance abuse, severe speech apraxia, or other neurological conditions affecting communication cannot join.
What is being tested?
The study is testing a new method to improve sentence formation and understanding in people with aphasia using 'implicit priming'. Researchers will first identify the most effective priming conditions for learning enhancement before developing and evaluating a novel treatment based on these initial findings.
What are the potential side effects?
Since this intervention involves language training exercises rather than medication or invasive procedures, traditional physical side effects are not expected. However, participants may experience fatigue or frustration during the learning process.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My hearing and vision are normal, or corrected to be normal.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have severe difficulty speaking clearly.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from baseline up to 1-week post training or 2-month post treatment
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from baseline up to 1-week post training or 2-month post treatment
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Comprehension of target sentences in a sentence-to-picture matching task
Production of target sentences on action description pictures
Real-time comprehension of target sentences in a sentence-to-picture matching task
Secondary study objectives
Connected speech production - picture description
Connected speech production - story retell
Production of untrained sentences on action describing pictures
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Structural priming trainingExperimental Treatment1 Intervention
Participants will be enrolled in 3 sessions of structural priming training (for experiment 1-3) or up to 15 treatment sessions (for experiment 4). Each session will be about 2 hour long, consisting of a set of tasks, including repeating, making, and remembering various types of sentences. In experiment 1-3, each participant will receive two different experimental priming conditions that are being compared within each session. In experiment 4, participants will receive a structural priming treatment in a single-subject design.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Implicit priming for Aphasia treatment uses subconscious cues to enhance sentence production and comprehension by leveraging the brain's residual language abilities. This method involves repeated exposure to specific linguistic patterns, helping to reactivate and strengthen neural pathways associated with language.
This approach is important for Aphasia patients as it offers a non-invasive and potentially more natural way to regain language skills, improving their communication abilities and overall quality of life.
Increasing aphasia treatment intensity in an acute inpatient rehabilitation program: A feasibility study.Evaluation of lexically and nonlexically based reading treatment in a deep dyslexic.
Increasing aphasia treatment intensity in an acute inpatient rehabilitation program: A feasibility study.Evaluation of lexically and nonlexically based reading treatment in a deep dyslexic.
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Who is running the clinical trial?
Purdue UniversityLead Sponsor
233 Previous Clinical Trials
71,274 Total Patients Enrolled
Temple UniversityOTHER
315 Previous Clinical Trials
88,888 Total Patients Enrolled
3 Trials studying Aphasia
448 Patients Enrolled for Aphasia
University of California, San DiegoOTHER
1,180 Previous Clinical Trials
1,574,943 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You currently have a problem with alcohol or drugs.I have severe difficulty speaking clearly.You have other conditions that affect how you communicate, like dementia.It's hard for you to talk in full sentences, and you can only say some words by themselves.You have mental health issues that are not being managed well.It has been over 6 months since I had a stroke affecting my left side.You have difficulty speaking after a stroke.It has been over 6 months since my stroke in the left side of my brain.I am a native English speaker.My hearing and vision are normal, or corrected to be normal.
Research Study Groups:
This trial has the following groups:- Group 1: Structural priming training
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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