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Status unknownNCT03635554ClinTALSAUpdated Apr 10, 2024

Translation and Clinical Implementation of a Test of Language and Short-term Memory in Aphasia

An observational study in Aphasia, sponsored by Temple University. Status unknown at 1 site in United States. Open to participants aged 21 Years to 80 Years. Per ClinicalTrials.gov, last updated 2024-04-10.

Sponsored by Temple University · Observational

The sponsor has not verified this record recently (last verified Apr 2024), so the status shown — last known as Enrolling by invitation — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
150
Ages
21 Years to 80 Years
Sex
All
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Study summary

This project aims to develop a clinically feasible version of a laboratory-developed assessment battery for language and verbal short-term memory difficulties in aphasia.

Read the detailed description

Over five years, we will develop a clinically feasible test that can be used to assess in-depth the language and verbal short-term memory abilities of individuals with aphasia (Called the TALSA - Temple Assessment of Language and Short-term memory in Aphasia. Based on a test that we have developed and tested over the past decade, we will create a shorter version that can be used by clinicians in a rehabilitation setting. The data to support this development will come from two sources: (1) clinicians in rehabilitation facilities who will use the new clinical test and provide feedback on the test (administration, value etc) and (2) people with aphasia who will be administered the longer version to help us identify the best test items in the laboratory version of the TALSA to be carried over to the shorter clinical version.

We are recruiting individuals with aphasia as well as people without aphasia (to serve as controls) to help with development of this assessment battery. The battery consists of between 15 and 20 subtests that assess many aspects of language and verbal short-term memory.

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Conditions studied

  • Aphasia

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Keywords

  • Aphasia
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In context

Aphasia

372 studies on the registry are indexed under Aphasia; 90 are open to participants now.

This study's planned enrollment of 150 is above the median of 74 across 43 observational studies indexed under Aphasia.

Browse Aphasia studies →

Lead sponsor

Temple University is the lead sponsor of 223 studies on the registry; 29 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 7 (58%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
21 Years to 80 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Participants with aphasia will have single or multiple left hemisphere lesions, but no right hemisphere lesions. They can be between the ages of 21 and 80. Their aphasia can range in severity from mild to severe and can be of any type except global aphasia. Their language output can be fluent or nonfluent and their comprehension can be mild moderately impaired.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • . single or multiple left hemisphere lesions
  • at least one year post-stroke.
  • high-school educated
  • negative histories for mental illness and alcohol/substance abuse.
  • passed an audiometric pure-tone, air conduction screening at 25 dB HL at 1K, 2K and 4K Hz for at least one ear.

Exclusion criteria

Exclusion Criteria:

English as a second language Right hemisphere stroke Less than 6 months post-onset of stroke.

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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
150 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Proportions correct on subtests of the Test of Language and Short-term Memory in Aphasia (TALSA)

    Participants will be administered 15-20 subtests of the TALSA that assess aspects of language (phoneme discrimination, sentence comprehension) and short-term memory (e.g., repetition span) abilities. Their responses on these measures will be evaluated in a item response analysis to determine which items are ideal to use in a smaller version of this test that is feasible to use in clinical practice. Another group of people with aphasia will be administered the clinical version (when it is complete) to develop normative data for that assessment battery.

    Time frame: two to three years December 1, 2017 through December 15, 2017 through November 30, 2022.

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Study locations

1 site
  • Temple University
    Philadelphia, Pennsylvania 19122, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 10, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03635554
Lead sponsor
Temple University
Responsible party
Nadine Martin (Professor Communication Sciences and Disorders, Temple University) — Principal investigator
First posted
Aug 17, 2018
Start date
Dec 15, 2017
Primary completion
Nov 30, 2025 (estimated)
Completion
Nov 30, 2025 (estimated)
Last update
Apr 10, 2024

Study contacts

Nadine Martin, Ph.D.
principal investigator · Temple University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.

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