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

Cognitive Reserve and Linguistic Resilience in Bilingual Hispanics With Primary Progressive Aphasia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05741853
Enrollment
60
Registered
2023-02-23
Start date
2023-05-01
Completion date
2027-11-30
Last updated
2026-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Disease, Aphasia, Apraxia, Motor, Bilingual Aphasia, Communication Disorders, Dementia, Dementia, Frontotemporal, Dysarthria, Frontotemporal Lobar Degeneration, Language Disorders, Neurocognitive Disorders, Neurodegenerative Diseases, Primary Progressive Aphasia, Speech Disorders

Keywords

Dementia, ADRD, Bilingualism, Multilingualism, Primary Progressive Aphasia, Bilingual Primary Progressive Aphasia, Cognitive Reserve, Language Decline, Bilingual Language Decline, Speech-Language Therapy, Bilingual Speech-Language Therapy, Spanish speakers, Spanish-Catalan Bilinguals, Spanish-English Bilinguals, Hispanic, Catalán, Catalan, Spanish, Castellano, Speech Therapy, Latino, Cognition

Brief summary

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.

Interventions

Participants with nonfluent/agrammatic variant primary progressive aphasia (PPA) or a predominantly nonfluent profile work on producing personally relevant scripts of 4-6 sentences in length. Length and complexity of scripts are individually tailored. The participant completes two (one hour each) teletherapy sessions per week with a clinician targeting clear and accurate script production, script memorization, and conversational usage of scripts. The participant completes 30 minutes of independent, computer-based practice 5-7 times per week, during which they speak in unison with a video/audio model of a healthy speaker clearly articulating the scripts.

Participants with logopenic variant PPA, participants with semantic variant PPA, and participants with a predominantly anomic profile will work on producing spoken and written names of personally relevant target items using a self-cueing hierarchy. Treatment focuses on the use of strategies that capitalize on spared cognitive-linguistic abilities to support word retrieval. The participant completes two (one hour each) teletherapy sessions per week with a clinician plus 30 minutes of additional independent, computer-based practice exercises 5-7 times per week.

Sponsors

Stephanie Grasso
Lead SponsorOTHER
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
CollaboratorOTHER
Hospital Clinic of Barcelona
CollaboratorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Meets diagnostic criteria for Primary Progressive Aphasia (PPA; Gorno-Tempini et al., 2011) * Bilingual in Spanish and Catalan or bilingual in Spanish and English * Different proficiency levels across languages are expected, any prior experience in both languages is acceptable * Intervention study: Score of 15 or higher on the Mini-Mental State Examination * Note that this project will also recruit individuals to participate in assessment only, for these individuals the following inclusion criteria applies: Score of 10 or higher on the Mini-Mental State Examination

Exclusion criteria

* Other central nervous system or medical diagnosis that can cause symptoms * Other psychiatric diagnosis that can cause symptoms * Significant, uncorrected visual or hearing impairment that would interfere with participation * Prominent initial non-speech-language impairments (cognitive, behavioral, motoric) * Intervention Study: Score of less than 15 on the Mini-Mental State Examination * Note that this project will also recruit individuals to participate in assessment only, for these individuals the following inclusion criteria applies: Score of less than 10 on the Mini-Mental State Examination

Design outcomes

Primary

MeasureTime frameDescription
Percent correct intelligible words from trained/untrained scriptsPre-phase 1, post-phase1/pre-phase 2 (4.5 weeks from treatment onset), post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatmentPercent of intelligible, scripted words for trained scripts and untrained scripts
Percent correct spoken naming of trained/untrained nounsPre-phase 1, post-phase1/pre-phase 2 (4.5 weeks from treatment onset), post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatmentPercent of correctly named trained pictured items and untrained pictured items

Secondary

MeasureTime frameDescription
Aphasia Impact Questionnaire (AIQ)Pre-phase 1, Post-phase 2 (9 weeks from treatment onset)Patient reported outcome measure for use with people with aphasia comprising three sections: activities, participation and emotional state/wellbeing. Uses a 5 point pictorial rating scale. The minimum score is 0 (best) and the maximum is 4 (worst).
Connected Speech Features: Type-token ratioPre-phase 1, Post-phase1/pre-phase 2 (4.5 weeks from treatment onset), Post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatmentTotal number of unique words (types) divided by the total number of words (tokens) derived from connected speech samples (script topic probes, picture description, and personal narrative).
Connected Speech Features: Mean length of utterancePre-phase 1, Post-phase1/pre-phase 2 (4.5 weeks from treatment onset), Post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatmentAverage number of words produced per utterance derived from connected speech samples (script topic probes, picture description, and personal narrative).
Acoustic Features: Articulation RatePre-phase 1, Post-phase1/pre-phase 2 (4.5 weeks from treatment onset), Post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatmentSyllables per second of phonated time derived from connected speech samples (script topic probes, picture description, and personal narrative).
Acoustic Features: Speech-to-pause timePre-phase 1, Post-phase1/pre-phase 2 (4.5 weeks from treatment onset), Post-phase 2 (9 weeks from treatment onset), 6 months and 1 year post-treatmentPhonated time divided by pause time in the sample derived from connected speech samples (script topic probes, picture description, and personal narrative).

Countries

Spain, United States

Contacts

CONTACTCamille Wagner Rodríguez, M.S., CCC-SLP
wagner.camille@austin.utexas.edu512-471-4119
PRINCIPAL_INVESTIGATORStephanie M Grasso, Ph.D

University of Texas at Austin

PRINCIPAL_INVESTIGATORMiguel Ángel Santos Santos, MD, PhD

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026