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NCT07260253 · ClinicalTrials.gov registry record · NA

Remotely-supervised Neuromodulation in PPA

A NA study of Primary Progressive Aphasia(PPA) and Logopenic Progressive Aphasia (LPA), sponsored by University of Texas at Austin.

Recruiting
Registry status
NA
Development phase
80
Enrollment target
2
Study locations

NCT07260253: Recruiting NA study of Primary Progressive Aphasia(PPA) and Logopenic Progressive Aphasia (LPA), sponsored by University of Texas at Austin.

NCT07260253 is a NA study of Primary Progressive Aphasia(PPA) and Logopenic Progressive Aphasia (LPA) that is actively recruiting participants, run by University of Texas at Austin. The registered enrollment target is 80 participants, below the 555-participant average among 3 other Primary Progressive Aphasia(PPA) trials with a reported enrollment target (86% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07260253, a NA study of Primary Progressive Aphasia(PPA) and Logopenic Progressive Aphasia (LPA), is actively recruiting participants, sponsored by University of Texas at Austin.

RECRUITING
Registry status
NA
Development phase
80 participants
Enrollment target
2
Study locations

Study Summary

The goal of this clinical trial is to learn whether remotely-supervised transcranial direct-current stimulation (RS-tDCS) can improve speech and language treatments for individuals with logopenic variant primary progressive aphasia (lvPPA). tDCS is a form of brain stimulation where a low-level electrical current is delivered to the brain through electrodes placed on the head. The main questions the trial aims to answer are: * Is it feasible to do RS-tDCS with virtual speech therapy? * How can brain magnetic resonance imaging scans (MRIs) predict how well someone will benefit from RS-tDCS with virtual speech therapy? Researchers will compare active RS-tDCS stimulation to sham stimulation (where there is no active stimulation, but participants feel stimulation effects at the beginning and end of the session). Participants will: * Travel to either the University of California, San Francisco (UCSF) or the University of Texas at Austin (UT Austin) one time for in-person testing, an MRI scan, and training on how to use the RS-tDCS equipment * Meet with a speech-language pathologist for pre-treatment testing on Zoom for 2 weeks * Participate in speech-language therapy and independent practice on Zoom 5 days a week for 4 weeks, using either active tDCS stimulation or sham * Complete post-treatment testing on Zoom for 1-2 weeks * Complete follow-up testing 2 months after completion of treatment

Primary Outcome

Change in percent correctly named trained/untrained pictures

Interventions

  • BEHAVIORAL Lexical Retrieval Cascade Treatment
  • DEVICE Remotely Supervised Transcranial Direct Current Stimulation

Study Locations (2)

California

  • UCSF Memory and Aging Cener - San Francisco

Texas

  • University of Texas - Austin

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2026-01
Est. Completion 2029-08
Phase NA
University of Texas at Austin

257 total trials

What NCT07260253 shows while recruiting

NCT07260253 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 555-participant average among 3 other Primary Progressive Aphasia(PPA) trials with a reported enrollment target (86% lower).

The record links to 6 conditions, with Primary Progressive Aphasia(PPA) appearing as the primary indexed condition, and to 2 interventions - of which Lexical Retrieval Cascade Treatment is the first listed.

NCT07260253 reports a single indexed study location in California, Texas.

Frequently Asked Questions

What is clinical trial NCT07260253 about?

NCT07260253 is a clinical study titled "Remotely-supervised Neuromodulation in PPA". The goal of this clinical trial is to learn whether remotely-supervised transcranial direct-current stimulation (RS-tDCS) can improve speech and language treatments for individuals with logopenic variant primary progressive aphasia (lvPPA). tDCS is a form of brain stimulation where a low-level elect...

What is the current status of trial NCT07260253?

This trial is currently recruiting. It is a NA study. The enrollment target is 80 participants. The study started on 2026-01. Estimated completion is 2029-08.

What conditions does trial NCT07260253 study?

This clinical trial studies the following conditions: Primary Progressive Aphasia(PPA), Logopenic Progressive Aphasia (LPA), Progressive Aphasia, Logopenic Variant Primary Progressive Aphasia, Logopenic Variant of Primary Progressive Aphasia (LPA).

What interventions are being tested in trial NCT07260253?

The interventions under investigation include: Lexical Retrieval Cascade Treatment (BEHAVIORAL), Remotely Supervised Transcranial Direct Current Stimulation (DEVICE).

Who is sponsoring clinical trial NCT07260253?

This trial is sponsored by University of Texas at Austin, which has 257 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07260253 being conducted?

This trial has 2 study locations across California, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT07260253, the US trial registry maintained by the National Library of Medicine. NCT07260253 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.