Balancing Effortful and Errorless Learning in Naming Treatment for Aphasia

ConditionsAphasiaStroke
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Pittsburgh

About this trial

Aphasia is a language disorder caused by stroke and other acquired brain injuries that affects over two million people in the United States and which interferes with life participation and quality of life. Anomia (i.e., word- finding difficulty) is a primary frustration for people with aphasia. Picture-based naming treatments for anomia are widely used in aphasia rehabilitation, but current treatment approaches do not address the long-term retention of naming abilities and do not focus on using these naming abilities in daily life. The current research aims to evaluate novel anomia treatment approaches to improve long-term retention and generalization to everyday life.

This study is one of two that are part of a larger grant. This record is for sub-study 1, which will adaptively balance effort and accuracy using speeded naming deadlines.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Existing diagnosis of chronic (>6 months) aphasia subsequent to left hemisphere ischemic or hemorrhagic stroke.

Impaired performance on 2/8 sections of the Comprehensive Aphasia Test.

Disqualifiers

History of other acquired or progressive neurological disease.

Significant language comprehension impairments

Unmanaged drug / alcohol dependence.

Severe diagnosed mood or behavioral disorders that require specialize mental health interventions.

Trial design

Design model

Crossover

Treatments tested in this trial

  • Accuracy-maximized condition

    Behavioral

    Naming treatment condition in which the target will be immediately provided for repetition at picture onset.

  • Effort-maximized condition

    Behavioral

    Naming treatment condition in which participants will have up to 10 seconds to respond before the target is provided for repetition.

  • Effort-accuracy balanced condition

    Behavioral

    Naming treatment condition in which naming deadlines will be determined based on the balanced effort-to-accuracy benefit ratio formalized above, calculated on clinician-provided accuracy and response time ratings. Deadlines will be recalculated session-by-session to adjust to participant-specific treatment gains over time.

Treatment groups

30 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Group A: Effort-maximized, then accuracy-maximized, then effort-accuracy balancedExperimental treatment 3 interventions
Group B: Effort-maximized, then effort-accuracy balanced, then accuracy-maximizedExperimental treatment 3 interventions
Group C: Accuracy-maximized, then effort-maximized, then effort-accuracy balancedExperimental treatment 3 interventions
Group D: Accuracy-maximized, then effort-accuracy balanced, then effort-maximizedExperimental treatment 3 interventions
Group E: Effort-accuracy balanced, then effort-maximized, then accuracy maximizedExperimental treatment 3 interventions
Group F: Effort-accuracy balanced, then accuracy-maximized, then effort-maximizedExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Change in correct responses in Confrontation Naming of Treated Pictured Objects

Confrontation naming accuracy of pictures targeted in each training condition will serve as a primary outcome. Individualized lists for each participant will be selected from a corpus of pictured objects. Performance will be evaluated twice at each timepoint. Change in performance from initial assessment to the 3-month follow-up timepoint on the treated items will serve as the primary outcome measure.

Time frame
Initial assessment (pre-treatment), 3 months post-treatment

Secondary outcomes

1

Change in correct responses in Confrontation Naming of Untreated Pictured Objects

Confrontation naming accuracy of pictured untreated items (matched for linguistic difficulty to treated items in the primary outcome) for each training condition will serve as a secondary outcome control condition.

Time frame
Initial assessment (pre-treatment), 3 months post-treatment
2

Change in correct responses in Context Generalization of Treated and Untreated Pictured Objects

Production of trained words on the context generalization complex scene description task for each training condition and corresponding untreated items will serve as a secondary outcome. Words from complex scenes and wordless picture books will be chosen for each participant. These words will consist of a subset of those selected for confrontation naming. Performance will be evaluated twice at each timepoint. Change in performance from initial assessment to the 3-month follow-up timepoint on the treated and untreated items will serve as a secondary outcome measure.

Time frame
Initial assessment (pre-treatment), 3 months post-treatment
3

Change in core lexicon analysis on the Aphasia Bank Discourse Protocol

The Aphasia Bank Discourse Protocol is a brief, but thorough set of language tasks which will characterize participants' language at the discourse level. The protocol requires participants to generate discourse samples within the contexts of free speech, a picture description, a story narrative, and procedural discourse. Change in performance in core lexicon analysis on discourse samples from initial assessment to each post-treatment follow up timepoint will serve as a secondary outcome measure.

Time frame
Initial assessment (pre-treatment), 3-months post-treatment
4

Change in mean scores on the Aphasia Communication Outcome Measure Short-Form

The Aphasia Communication Outcome Measure (ACOM) is a measure of patient-reported "communication functioning," defined as the ability to effectively convey and receive personally relevant messages in natural environments. Results are provided in T scores (sample mean of 50 with a standard deviations of 10), with higher scores indicating better communication functioning.

Time frame
Initial assessment (pre-treatment), 1 week post-treatment.

Other outcomes

Sponsors and contacts

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University of Pittsburgh

Lead sponsor

University of Massachusetts, Amherst

Collaborator

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborator