MedPath

Analysis of Brain Activity to Uncover Brain-behavior Relationships Related to Therapy Outcomes in Aphasia

Not Applicable
Completed
Conditions
Aphasia
Interventions
Behavioral: Abstract Semantic Association Network Training (AbSANT)
Registration Number
NCT03550092
Lead Sponsor
Penn State University
Brief Summary

Aphasia is a loss of language due to stroke or other brain injury. Word-finding in conversation is a universal and persistent difficulty in aphasia. While several techniques exist to improve word-finding in aphasia, it is unclear how the brain changes in response to behavioral therapy. In this study, persons with aphasia will receive behavioral therapy aimed at helping them to be more successful at finding words. Twenty therapy sessions will be provided in a 10-week period. Each therapy session will last about 2 hours and will include a variety of language tasks. Prior to beginning word-finding therapy, each participant will receive two fMRI scans, spaced 10 weeks apart. After finishing therapy, each participant will receive two additional fMRI scans, spaced 10 weeks apart. For a portion of the MRI scan, participants will complete language tasks. The purpose of these fMRI scans is to measure brain changes that may occur due to successful behavioral therapy. The hypotheses are as follows: First, that the behavioral therapy will improve word-finding as it has been shown to do in the past. Second, that the brain will change in a couple of different ways. It is expected that the network of regions that support word-finding will be more connected and work together more efficiently after therapy. It is also expected that the networks of regions that support other aspects of cognitive function, such as attention and executive function, will also be more connected and work together more efficiently.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
23
Inclusion Criteria
  1. Diagnosis of aphasia
  2. Sustained stroke more than 6 months prior to consent
  3. Right-handed
  4. Native speakers of English
  5. Completed at least a high school education
  6. Normal or corrected-to-normal vision and hearing
  7. Provide written informed consent
  8. Participants will be medically stable and at least wheelchair ambulatory at the time of participation with uncompromised use of the left hand
Exclusion Criteria
  1. History of degenerative neurological disorders (e.g., Alzheimer's disease), acquired neurological disorders other than aphasia from stroke (e.g., traumatic brain injury), developmental neurological disorders (e.g., autism), or psychiatric disorders
  2. An active medical condition that could compromise participation (e.g., cancer undergoing acute treatment)
  3. Not safe to enter the bore of the magnet (e.g., pacemaker)
  4. Taking medications that are known to exert significant effects on cognitive processes
  5. Pregnancy or possibility of pregnancy
  6. Do not meet the above inclusionary criteria

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
AphasiaAbstract Semantic Association Network Training (AbSANT)Abstract Semantic Association Network Training (AbSANT) Each session will be 2 hours long and will occur twice each week for a total of 20 sessions.
Primary Outcome Measures
NameTimeMethod
Therapy Effect Size: Change in word generation performance from pre- to post-treatment measured using a version of Cohen's dAt baseline and at approximately 10 weeks (i.e., the end of therapy)

The mean of the baseline scores is subtracted from the mean of the post-treatment scores, and then divided by the standard deviation (SD) of the baseline scores. 6.5-8 is considered a small effect size, 8-9.5 is medium, and above 9.5 is large.

Change in fMRI activation patters from pre- to post-treatmentAt baseline and at approximately 10 weeks (i.e., the end of therapy)

Blood-oxygen-level-dependent MRI signal measured during task and rest and subjected to statistical tests of significant change from pre- to post-treatment.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hershey Medical Campus

🇺🇸

Hershey, Pennsylvania, United States

© Copyright 2025. All Rights Reserved by MedPath