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Cued Picture-Naming Therapy for Aphasia
N/A
Recruiting
Led By Stacy M Harnish, PhD
Research Sponsored by Ohio State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Native English Speaker.
At least six months post-onset of a single left-hemisphere stroke
Must not have
Severe depression
Diffuse injury or disease of the brain
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 months
Awards & highlights
No Placebo-Only Group
Summary
This trial will investigate whether genes and cognitive abilities predict responsiveness to aphasia therapy for word-retrieval difficulties.
Who is the study for?
This trial is for native English speakers who have chronic aphasia, specifically difficulty retrieving words (anomia), due to a single left-hemisphere stroke that occurred at least six months ago. It's not suitable for those with severe comprehension issues, depression, MRI contraindications like pacemakers or metal implants, claustrophobia, pregnancy, severe speech disorders, widespread brain damage or uncorrected vision/hearing problems.
What is being tested?
The study is exploring the effectiveness of cued picture-naming therapy in treating word-retrieval difficulties in people with aphasia. It aims to determine if two specific genes and cognitive abilities such as memory can predict how well someone will respond to this treatment.
What are the potential side effects?
Since the intervention involves non-invasive therapy sessions focused on language recovery rather than medication or surgery, there are no direct physical side effects expected from the cued picture-naming therapy itself.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am a native English speaker.
Select...
It has been over 6 months since my stroke in the left side of my brain.
Select...
I struggle to find the right words when speaking.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have severe depression.
Select...
I have widespread brain damage or disease.
Select...
I have vision or hearing problems that haven't been corrected.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Percent of pictures named correctly
Percentage of pictures named correctly
Secondary study objectives
Percentage of untrained pictures named correctly
percentage of definitions named correctly
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: Single Arm TreatmentExperimental Treatment1 Intervention
Cued picture naming therapy will be delivered to all participants. There will be four cohorts of participants based on BDNF and ApoE genotypes.
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Who is running the clinical trial?
Ohio State UniversityLead Sponsor
866 Previous Clinical Trials
655,004 Total Patients Enrolled
1 Trials studying Aphasia
20 Patients Enrolled for Aphasia
Nationwide Children's HospitalOTHER
348 Previous Clinical Trials
5,227,949 Total Patients Enrolled
Stacy M Harnish, PhDPrincipal InvestigatorOhio State University
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a serious difficulty understanding spoken language.I am a native English speaker.It has been over 6 months since my stroke in the left side of my brain.You have a serious difficulty speaking clearly.I have severe depression.I struggle to find the right words when speaking.Difficulty speaking that has lasted a long time.I have widespread brain damage or disease.I have vision or hearing problems that haven't been corrected.
Research Study Groups:
This trial has the following groups:- Group 1: Single Arm Treatment
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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