Aphasia Rehabilitation: Modulating Cues, Feedback & Practice
NCT ID: NCT01597037
Last Updated: 2018-11-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
16 participants
INTERVENTIONAL
2011-06-30
2018-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Studying Language With Brain Stimulation in Aphasia
NCT05660304
Speech and Language Therapy After Stroke
NCT00713050
Augmenting Language Therapy for Aphasia: Levodopa
NCT01429077
Modeling Treated Recovery From Aphasia
NCT03416738
Dosage and Predictors of Naming Treatment Response in Aphasia
NCT02005016
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
A common neurological deficit among stroke survivors, and thus a substantial contributor to post-stroke disability, is aphasia. The loss of, or difficulty with language is extremely debilitating. Recently, there has been an emphasis on the need for intensive aphasia treatment in order to make the long-term neuroplastic changes associated with recovery. However, specific information regarding effective learning parameters is limited.
A number of variables and practice conditions, deriving from motor learning theory, potentially impact the rehabilitation process. Several of these variables have begun to be addressed in the literature, but with conflicting or scant evidence to date. Variables include the type and degree of external cueing, low versus high feedback conditions, task complexity, and practice distribution and schedule.
The purpose of this study is to:
* Modulate variables of cuing, feedback and script complexity that potentially affect treatment outcomes, and measure their effects on acquisition, maintenance and generalization of script learning. These investigations are conducted as separate studies, with the first study being a cross-over study investigating cuing and the second study being a 2x2 factorial design investigating feedback and complexity.
* Modify and optimize AphasiaScripts-an existing treatment program having experimental support for its efficacy-by incorporating these findings.
* Conduct a clinical trial, incorporating the optimized AphasiaScripts program, in order to measure the effect of massed vs distributed practice, and blocked vs random practice schedules, on the acquisition, maintenance and generalization of script learning.
Measures will include independent pre-and post assessments of acquisition, maintenance and generalization of script learning as well as dependent item/cue level measures of progress.
Results and computational models of acquisition, maintenance and generalization will contribute new evidence to support not just the efficacy and delivery of AphasiaScripts, but also the application of practice principles to aphasia treatment in general.
The first part of the study - a cross-over study that evaluates error-free versus error-reducing script training has been done. Below is a description of the second part of the study which evaluates feedback and script complexity.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
High complexity, high feedback
Scripts are one grade level higher than the typical script that would be provided for the severity of aphasia; there is an opportunity for the participant to listen to his/her production and assess performance.
Script training
90 minutes/day, 6 days a week; includes 3 weeks of training
High complexity, low feedback
Scripts are one grade level higher than the typical script that would be provided for the severity of aphasia; there is no opportunity for the participant to listen to his/her production and assess performance.
Script training
90 minutes/day, 6 days a week; includes 3 weeks of training
Low complexity, high feedback
Scripts are one grade level lower than the typical script that would be provided for the severity of aphasia; there is an opportunity for the participant to listen to his/her production and assess performance.
Script training
90 minutes/day, 6 days a week; includes 3 weeks of training
Low complexity, low feedback
Scripts are one grade level lower than the typical script that would be provided for the severity of aphasia; there is no opportunity for the participant to listen to his/her production and assess performance.
Script training
90 minutes/day, 6 days a week; includes 3 weeks of training
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Script training
90 minutes/day, 6 days a week; includes 3 weeks of training
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Aphasia Quotient between 40 and 80 on the Western Aphasia Battery
* Age 21 or older
* At least 6 months post-stroke
* Able to comply with the study protocol
* Premorbidly right-handed, as determined by the Edinburgh Handedness Inventory
* Fluent in English premorbidly
* Completed at least 8th grade education
Exclusion Criteria
* Any other neurological condition that could potentially affect cognition, speech or language.
* Global aphasia or inability to participate in routine speech therapy
* Major active psychiatric illness that may interfere with required study procedures
* Untreated or inadequately treated depression
* Current abuse of alcohol or drugs
* Unable to understand, cooperate or comply with study procedures
* Significant visual or auditory impairment
18 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Colorado, Boulder
OTHER
Shirley Ryan AbilityLab
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Leora Cherney
Senior Research Scientist
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Center for Aphasia Research & Treatment, Rehabilitation Institute of Chicago
Chicago, Illinois, United States
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Cherney LR, Van Vuuren S. Complexity and Feedback During Script Training in Aphasia: A Feasibility Study. Arch Phys Med Rehabil. 2022 Jul;103(7S):S205-S214. doi: 10.1016/j.apmr.2022.03.002. Epub 2022 Mar 15.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.