80 Participants Needed

Neuromodulation for Primary Progressive Aphasia

Recruiting at 1 trial location
AL
Overseen ByAphasia Lab Research Coordinator
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Texas at Austin
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores whether remotely-supervised transcranial direct-current stimulation (RS-tDCS) can enhance speech therapy for individuals with logopenic variant primary progressive aphasia (lvPPA). The researchers aim to determine if this stimulation, combined with virtual speech therapy, can improve speech and if MRI scans can predict who will benefit most. Participants will receive either active brain stimulation or a sham (inactive) version while engaging in online speech exercises. The trial seeks individuals diagnosed with lvPPA who have reliable internet access and can work with a study partner. Participants should be comfortable using a computer and willing to undergo an MRI scan. As an unphased trial, this study offers a unique opportunity to contribute to groundbreaking research that could enhance future treatment options.

Do I need to stop my current medications for the trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What prior data suggests that remotely-supervised transcranial direct-current stimulation is safe for individuals with primary progressive aphasia?

Research has shown that remotely supervised transcranial direct current stimulation (RS-tDCS) is generally safe and well-tolerated. In past studies, RS-tDCS safely improved language, movement, and thinking skills in patients, including those recovering from strokes. This method applies a small electrical current to the brain, which participants have managed well. No serious side effects were reported, suggesting that RS-tDCS can be a safe option for people considering joining such trials.12345

Why are researchers excited about this trial?

Researchers are excited about transcranial direct current stimulation (tDCS) for primary progressive aphasia because it offers a unique, non-invasive approach to enhancing brain function. Unlike traditional speech therapy alone, tDCS delivers a small electrical current to specific brain areas, potentially boosting the effectiveness of virtual speech-language training. Moreover, this method allows for remote supervision, making it convenient for patients to receive therapy in their own homes. This combination of brain stimulation with language therapy could lead to significant improvements in communication skills for individuals with this challenging condition.

What evidence suggests that remotely-supervised transcranial direct-current stimulation is effective for primary progressive aphasia?

Research has shown that transcranial direct current stimulation (tDCS) might improve language skills in people with primary progressive aphasia (PPA). In this trial, participants will receive either active tDCS or sham stimulation while engaging in virtual speech-language training. One study found that tDCS combined with speech and language therapy led to better language outcomes, suggesting that tDCS can enhance the effects of language therapy. Another study demonstrated that tDCS helped with tasks involving short-term memory for words, a common challenge for people with PPA. These findings support the idea that tDCS might enhance speech therapy effectiveness for people with PPA, including those with the logopenic variant.13678

Who Is on the Research Team?

ML

Maya L Henry, PhD

Principal Investigator

University of Texas at Austin

Are You a Good Fit for This Trial?

This trial is for individuals with a speech and language disorder called logopenic variant primary progressive aphasia (lvPPA). Participants must be able to travel once to UCSF or UT Austin, use RS-tDCS equipment after training, and commit to virtual therapy sessions. Specific inclusion and exclusion criteria details are not provided.

Inclusion Criteria

I have been diagnosed with logopenic variant primary progressive aphasia.
My hearing and vision are good, with aids if I use them.
I am willing and able to have an MRI scan of my brain.
See 5 more

Exclusion Criteria

Speech and language deficits better accounted for by another neurological disorder
I have had a stroke, epilepsy, or significant brain injury.
I do not have a diagnosis of logopenic variant primary progressive aphasia.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1 visit
1 visit (in-person)

Pre-treatment

Participants meet with a speech-language pathologist for pre-treatment testing on Zoom

2 weeks
Virtual meetings

Treatment

Participants engage in speech-language therapy and independent practice on Zoom using either active tDCS stimulation or sham

4 weeks
5 sessions per week (virtual)

Post-treatment

Participants complete post-treatment testing on Zoom

1-2 weeks
Virtual meetings

Follow-up

Participants complete follow-up testing 2 months after completion of treatment

2 months
Virtual meetings

What Are the Treatments Tested in This Trial?

Interventions

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

Trial Overview

The study tests if remotely-supervised transcranial direct-current stimulation (RS-tDCS) combined with virtual speech therapy can help improve communication in lvPPA patients. It compares active brain stimulation against sham stimulation alongside regular speech-language treatment over Zoom.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: Language Therapy with Active StimulationExperimental Treatment2 Interventions
Group II: Language Therapy with Sham StimulationPlacebo Group2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Texas at Austin

Lead Sponsor

Trials
387
Recruited
86,100+

National Institute on Aging (NIA)

Collaborator

Trials
1,841
Recruited
28,150,000+

Citations

Speech-Language Treatment With Remotely Supervised ...

The study will evaluate the feasibility and preliminary benefit of home-based transcranial direct current stimulation (tDCS) combined with evidence-based speech ...

Home-Based Transcranial Direct Current Stimulation in ...

Conclusions: These preliminary results indicate that vSTM/WM intervention can improve performance in trained vSTM/WM tasks in patients with PPA, especially when ...

Remotely Supervised Home-based tDCS Augmentation of ...

Results showed improvements in language outcomes, suggesting the potential of tDCS as an augmentation to speech and language therapy (SLT) in PPA management.

a double-blind sham-controlled study

Transcranial direct current stimulation (tDCS) has generated some promising outcomes in primary progressive aphasia (PPA). The logopenic variant (lv-PPA), ...

NCT05615922 | Remotely Supervised Transcranial Direct ...

This study will evaluate whether RS-tDCS combined with language skills practice is a feasible study design for individuals with PPA. Official Title. Remotely ...

Remotely Supervised Transcranial Direct Current ...

RS-tDCS is safe and feasible, affording beneficial effects in the motor, language, and cognitive functions of patients with post-stroke impairments.

Feasibility of home-based transcranial direct current ...

We evaluated the feasibility of providing an intervention combining tDCS with SLT as a home-based and remotely supervised intervention.

Feasibility of Home-Based Transcranial Direct Current ...

Conclusions: Overall, this study demonstrates the feasibility and potential benefit of a novel, easily accessible and patient-relevant telerehabilitation ...