Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
Healthy Volunteers
NCT05741853

Cognitive Reserve and Response to Speech-Language Intervention in Bilingual Speakers With Primary Progressive Aphasia

Led by University of Texas at Austin · Updated on 2025-11-12

60

Participants Needed

3

Research Sites

239 weeks

Total Duration

On this page

Sponsors

U

University of Texas at Austin

Lead Sponsor

F

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Collaborating Sponsor

AI-Summary

What this Trial Is About

Difficulties with speech and language are the first and most notable symptoms of primary progressive aphasia (PPA). While there is evidence that demonstrates positive effects of speech-language treatment for individuals with PPA who only speak one language (monolinguals), there is a significant need for investigating the effects of treatment that is optimized for bilingual speakers with PPA. This stage 2 efficacy clinical trial seeks to establish the effects of culturally and linguistically tailored speech-language interventions administered to bilingual individuals with PPA. The overall aim of the intervention component of this study is to establish the relationships between the bilingual experience (e.g., how often each language is used, how "strong" each language is) and treatment response of bilinguals with PPA. Specifically, the investigators will evaluate the benefits of tailored speech-language intervention administered in both languages to bilingual individuals with PPA (60 individuals will be recruited). The investigators will conduct an assessment before treatment, after treatment and at two follow-ups (6 and 12-months post-treatment) in both languages. When possible, a structural scan of the brain (magnetic resonance image) will be collected before treatment in order to identify if brain regions implicated in bilingualism are associated with response to treatment. In addition to the intervention described herein, 30 bilingual individuals with PPA will be recruited to complete behavioral cognitive-linguistic testing and will not receive intervention. Results will provide important knowledge about the neural mechanisms of language re-learning and will address how specific characteristics of bilingualism influence cognitive reserve and linguistic resilience in PPA.

CONDITIONS

Official Title

Cognitive Reserve and Response to Speech-Language Intervention in Bilingual Speakers With Primary Progressive Aphasia

Who Can Participate

Age: 40Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with Primary Progressive Aphasia (PPA) according to specified criteria
  • Bilingual in Spanish and Catalan or Spanish and English
  • Acceptable to have different proficiency levels or prior experience in both languages
  • For intervention participants, Mini-Mental State Examination score of 15 or higher
  • For assessment-only participants, Mini-Mental State Examination score of 10 or higher
Not Eligible

You will not qualify if you...

  • Other central nervous system or medical diagnoses causing symptoms
  • Other psychiatric diagnoses causing symptoms
  • Significant, uncorrected visual or hearing impairments that interfere with participation
  • Prominent initial impairments not related to speech-language (cognitive, behavioral, motoric)
  • For intervention participants, Mini-Mental State Examination score below 15
  • For assessment-only participants, Mini-Mental State Examination score below 10

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 3 locations

1

University of Texas at Austin

Austin, Texas, United States, 78752

Actively Recruiting

2

Hospital de la Santa Creu i Sant Pau

Barcelona, Spain, 08025

Actively Recruiting

3

Hospital Clínic de Barcelona

Barcelona, Spain, 08036

Not Yet Recruiting

Loading map...

Research Team

C

Camille Wagner Rodríguez, M.S., CCC-SLP

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here