Remotely-supervised Neuromodulation in PPA
NCT07260253 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80
Last updated 2026-05-06
Summary
The goal of this clinical trial is to learn whether home-based brain stimulation combined with virtual speech-language therapy can improve communication abilities in adults with logopenic variant primary progressive aphasia (lvPPA), a language disorder most often caused by Alzheimer's disease.
The main questions the study aims to answer are:
* Is combining remotely supervised transcranial direct current stimulation (tDCS) with virtual speech-language therapy feasible and acceptable for people with lvPPA?
* Does this combined treatment lead to improvements in communication compared to speech-language therapy with sham (placebo) stimulation?
* Do individual brain characteristics help predict who benefits most from this treatment?
Researchers will compare participants who receive active tDCS plus virtual speech-language therapy to participants who receive sham (placebo) tDCS plus virtual speech-language therapy to see if active brain stimulation enhances communication outcomes.
Participants will:
* Complete speech-language therapy sessions delivered by video visit.
* Receive either active or sham tDCS that is remotely supervised and completed at home.
* Complete language and cognitive testing before and after treatment.
* Undergo brain imaging and other assessments to help understand treatment response.
Conditions
- Primary Progressive Aphasia(PPA)
- Progressive Aphasia
- Progressive Aphasia in Alzheimer's Disease
- Logopenic Progressive Aphasia (LPA)
- Logopenic Variant Primary Progressive Aphasia
- Logopenic Variant of Primary Progressive Aphasia (LPA)
Interventions
- BEHAVIORAL
-
Lexical Retrieval Cascade Treatment
Participants work on producing spoken and written names of personally-relevant target items. 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 3 times per week.
- DEVICE
-
Remotely Supervised Transcranial Direct Current Stimulation- Active
tDCS is a type of non-invasive brain stimulation. 2.0 milliamp (mA) of current will be delivered via electrodes in saline-soaked sponges placed on the left and right sides of the head. The stimulation will last 20 minutes and will occur 5 times weekly, in the participant's home setting, while the participant engages in computer-delivered speech-language training. Sessions are monitored by study personnel.
- DEVICE
-
Remotely Supervised Transcranial Direct Current Stimulation - Sham
tDCS is a type of non-invasive brain stimulation. 2.0 milliamp (mA) of current will be delivered via electrodes in saline-soaked sponges placed on the left and right sides of the head. In sham stimulation, current will be delivered for a brief period of time and then turned off. Sham stimulation will last 20 minutes and will occur 5 times weekly, in the participant's home setting, while the participant engages in computer-delivered speech-language training. Sessions are monitored by study personnel.
Sponsors & Collaborators
-
National Institute on Aging (NIA)
collaborator NIH -
Maya Henry
lead OTHER
Principal Investigators
-
Maya L Henry, PhD · University of Texas at Austin
-
Jessica D Richardson, PhD · University of New Mexico
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-04-15
- Primary Completion
- 2029-05-31
- Completion
- 2029-08-31
Countries
- United States
Study Locations
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