What this study is
The goal of this clinical trial is to determine whether individually tailored speech-language telerehabilitation helps improve communication in people with primary progressive aphasia (PPA), a form of dementia that affects speech and language. The study will be offered to individuals who speak English and/or Spanish. The study will also document how acceptable and beneficial the program is to both patients and their care partners.
The main questions the study aims to answer are:
1. Is the telerehabilitation program feasible and acceptable for people with PPA and their care partners? 2. Do participants with PPA and care partners find treatment beneficial? 3. Which outcome measures are most useful for evaluating changes in communication and quality of life? 4. What patterns of treatment response are seen in participants after completing the program?
The program includes both speech-language therapy and training for care partners.
Participants with PPA will:
1. Complete virtual communication tasks and questionnaires before and after the program 2. Take part in online speech-language therapy sessions 3. Include their care partners in some parts of the program for training and support
What's being tested
- Multicomponent Lexical Retrieval Training
Intervention · BEHAVIORAL
In person or via teletherapy: A multi-component treatment incorporating elements of restitutive, compensatory, and care-partner focused interventions. Participants work on producing names of personally relevant target in multiple communication modalities. Biweekly (approximately one hour each) sessions with a clinician target multimodal communication and the use of strategies to support word retrieval. These skills are also trained via daily independent practice. The participant meets four times during the course of treatment with a study partner (e.g., spouse) for communication counseling, education, and practice of communication strategies.
- Multicomponent Video Implemented Script Training in Aphasia
Intervention · BEHAVIORAL
In person or via teletherapy: A multi-component treatment incorporating elements of restitutive, compensatory, and care-partner focused interventions. Treatment focuses on production of individually-tailored, personally relevant scripts. The participant completes 30 minutes per day of independent practice, during which they speak in unison with a video model. Biweekly (approximately one hour each) sessions with a clinician target clear and accurate script production, memorization, and conversational usage, as well as multimodal communication. The participant meets 6 times during the course of treatment with a study partner (e.g., spouse) for communication counseling, education, and practice of communication strategies.
Study details
- Official title
- Intervention to Promote Communication Quality of Life for Persons With Language-Led Dementia and Their Partners: A Randomized Pilot Trial
- Sponsor
- University of Texas at Austin
- Conditions
- Primary Progressive Aphasia(PPA) · Semantic Dementia · Logopenic Progressive Aphasia (LPA) · Nonfluent Aphasia, Progressive · Progressive Aphasia · Semantic Variant Primary Progressive Aphasia (svPPA) · Semantic Aphasia · Logopenic Variant Primary Progressive Aphasia · Logopenic Variant of Primary Progressive Aphasia (LPA) · Logopenic Progressive Aphasia · Nonfluent Variant Primary Progressive Aphasia (nfvPPA) · Nonfluent Progressive Aphasia
- Enrolling
- 25 people
- Starts
- 2026-01-03
- Est. completion
- 2027-08
- Design
- Open-label, randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 40 Years and overSex ALLHealthy volunteers Not acceptedPersons with PPA
You may qualify if
- A PPA (Gorno-Tempini et al., 2011) or "PPA-plus" (Mesulam et al., 2001) diagnosis
- MMSE score of > 15 and must be able to produce single monosyllabic words intelligibly.
- Must speak English, Spanish or both languages (i.e., bilingual speakers of English or Spanish)
- Hearing and vision adequate for participation in teleconference meetings
- Must have a care partner available (someone who will commit to attending teleconference sessions weekly during treatment phases)
You can't join if
- Other central nervous system or medical diagnosis that can account for symptoms
- Psychiatric diagnosis that can account for symptoms
- The participant and/or study partner must have basic experience using a computer.
Care Partners
You may qualify if
- Partners must express willingness to attend and participate in treatment sessions including those targeting dyadic communication goals
- Partners must speak English, Spanish or both languages (i.e., bilingual speakers of English or Spanish)
- Partner's hearing and vision should be adequate for participation in teleconference meetings
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openUniversity of Texas
Austin, Texas, United States
- Carly M Millanski, MS · Contact512-471-3420aphasialab@austin.utexas.edu
- Camille Wagner Rodriguez, MS · Contactwagner.camille@austin.utexas.edu
- Maya L Henry, PhD · Principal investigator
- Stephanie M Grasso, PhD · Principal investigator
Recruiting
Study team
Sponsor
University of Texas at Austin
Study ID R61AG089318
Principal investigator
Maya L Henry, PhD
University of Texas at Austin
Principal investigator
Stephanie M Grasso, PhD
University of Texas at Austin
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.