Remotely-supervised Neuromodulation in PPA

NCT07260253 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-05-06

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07260253 on ClinicalTrials.gov