Effects of Aphasia Identification Cards on Service Workers' Comprehension of People With Aphasia
PAUSE
2 other identifiers
interventional
160
1 country
1
Brief Summary
The goal of this clinical trial is to learn whether healthy volunteers are more successful at understanding people with aphasia if they have first viewed an aphasia identification (ID) card. The main questions this study aims to answer are:
- Does viewing an aphasia ID card improve healthy volunteers' understanding of the language errors made by people with aphasia?
- Does viewing an aphasia ID card improve healthy volunteers' understanding of people with aphasia who make long pauses in their speech? Researchers will compare aphasia ID cards to a control condition (no ID card) to see whether aphasia ID cards improve healthy volunteers' understanding. Healthy volunteers will visit the study site for a single session (about 2 hours long). During the session they will:
- Complete brief tests of their vision, hearing and thinking
- Listen to sentences produced by a speaker with aphasia while their eye movements are recorded
- Complete a survey about the experience of listening to the speaker with aphasia
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 1, 2025
CompletedFirst Posted
Study publicly available on registry
May 25, 2025
CompletedStudy Start
First participant enrolled
September 22, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
April 29, 2026
April 1, 2026
10 months
May 1, 2025
April 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Comprehension accuracy for sentences with long pauses in the Service Request Comprehension Task
Percent correct mouse-click responses on the Service Request Comprehension Task for sentences with long pauses. The Service Request Comprehension Task measures participants' comprehension and processing of language produced by a speaker with aphasia.
5 minutes post-intervention
Comprehension accuracy for sentences with paraphasias in the Service Request Comprehension Task
Percent correct mouse-click responses on the Service Request Comprehension Task for sentences with paraphasias (word-retrieval errors). The Service Request Comprehension Task measures participants' comprehension and processing of language produced by a speaker with aphasia.
5 minutes post-intervention
Secondary Outcomes (6)
Visual attention during long pauses in the Service Request Comprehension Task
5 minutes post-intervention
Linguistic integration of words immediately following long pauses in the Service Request Comprehension Task
5 minutes post-intervention
Implicit repair of paraphasias in the Service Request Comprehension Task
5 minutes post-intervention
Rating of own patience on the Attitude Survey
0 minutes (immediately) post-intervention, 45 minutes post-intervention
Rating of speaker with aphasia's intelligence on the Attitude Survey
0 minutes (immediately) post-intervention, 45 minutes post-intervention
- +1 more secondary outcomes
Study Arms (2)
Aphasia Identification Card
EXPERIMENTALParticipants will view an aphasia ID card for a speaker with aphasia. The card will disclose the speaker's aphasia, define aphasia, and request time to communicate.
No Card
NO INTERVENTIONParticipants in this arm will not receive an intervention.
Interventions
Participants will view an aphasia ID card for a speaker with aphasia. The card will disclose the speaker's aphasia, define aphasia, and request time to communicate.
Eligibility Criteria
You may qualify if:
- Adult age 18-59
- Currently employed as a service worker
- Understand spoken and written English well
- High school diploma or equivalency
- Normal vision or corrected vision with glasses or contact lenses
You may not qualify if:
- Language disorder
- Hearing impairment
- Intellectual disability
- History of acquired neurological disorder (e.g., stroke or moderate/severe brain injury)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
UMass Amherst Henry M. Thomas III Center at Springfield
Springfield, Massachusetts, 01115, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jennifer Mack, PhD
University of Massachusetts, Amherst
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
May 1, 2025
First Posted
May 25, 2025
Study Start
September 22, 2025
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
April 29, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- De-identified data will be available upon publication of related work or the end of the project period, whichever comes first, and will remain available indefinitely.
- Access Criteria
- IPD and supporting information will be freely available on Open Science Framework.
Data to be generated from this project include language processing data collected through eye-tracking, comprehension accuracy data (mouse-click responses), and participants' responses to a survey measuring their attitudes. De-identified raw survey data and comprehension accuracy data will be preserved and shared. Deidentified, preprocessed eye-tracking data will be preserved and shared.