Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
ID07260253

Investigating the Benefits of Remotely-Supervised Neuromodulation In Primary Progressive Aphasia

Led by Maya Henry · Updated on 2026-05-06

80

Participants Needed

2

Research Sites

13 weeks

Total Duration

On this page

Sponsors

M

Maya Henry

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying adults with logopenic variant primary progressive aphasia (lvPPA), a language disorder often linked to Alzheimer's disease, to see if combining remotely supervised brain stimulation with virtual speech-language therapy improves communication. The study aims to determine whether this combined treatment is feasible, acceptable, and more effective than speech therapy with placebo stimulation. It also explores if individual brain features can predict who benefits most from the therapy. Participants will be assigned randomly to receive either active or sham transcranial direct current stimulation (tDCS) alongside virtual speech-language therapy. The active tDCS involves 20-minute sessions of non-invasive brain stimulation delivered at home five times a week while engaging in computer-based speech training. The speech therapy includes two teletherapy sessions weekly plus independent practice exercises. Both treatment groups will be monitored remotely during sessions. Throughout the study, participants will complete language and cognitive tests before and after treatment, plus brain imaging and other evaluations to understand treatment effects. Researchers will measure changes in spoken naming ability at one and three months after treatment begins. Additional assessments include communication confidence, aphasia impact, and treatment acceptability. Participation involves regular video visits, remote supervision, and testing over several months.

CONDITIONS

Brief Title

Remotely-supervised Neuromodulation in PPA

Who Can Participate

Age: 40Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Meets diagnostic criteria for primary progressive aphasia (PPA)
  • Meets diagnostic criteria for logopenic variant PPA
  • Scores 20 or higher on the Mini-Mental State Examination
  • Has adequate hearing and vision (with aids if needed)
  • Able to travel to research site and undergo MRI brain scan
  • Has access to high-speed internet and basic computer/internet experience
  • Is a fluent English speaker
  • Has a study partner who can co-enroll, attend pre-treatment training, and be present for teleconference meetings
Not Eligible

You will not qualify if you...

  • Speech and language deficits explained by another neurological disorder
  • Does not meet diagnostic criteria for logopenic variant PPA
  • Scores less than 20 on the Mini-Mental State Examination
  • Does not have a study partner who can co-enroll
  • Has contraindications for tDCS or MRI (history of seizures, head injury, skull surgery, severe migraines, metal implants, pacemaker, chronic skin problems, pregnancy)
  • History of stroke, epilepsy, or significant brain injury

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - Duration of treatment period as per study schedule

Participants receive virtual language therapy combined with remotely-supervised transcranial direct current stimulation or sham stimulation at home. Treatment includes two one-hour teletherapy sessions per week plus 30 minutes of independent computer-based practice exercises three times per week. The brain stimulation occurs five times weekly during speech-language training sessions.

Multiple remote sessions weekly including 2 teletherapy sessions and 5 stimulation sessions per week

Trial Site Locations

Total: 2 locations

1

UCSF Memory and Aging Cener

San Francisco, California, United States, 94158

Actively Recruiting

2

University of Texas

Austin, Texas, United States, 78712

Actively Recruiting

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Research Team

A

Aphasia Lab Research Coordinator

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Treatment for Word Retrieval in Semantic and Logopenic Variants of Primary Progressive Aphasia: Immediate and Long-Term Outcomes.

Maya L Henry, H Isabel Hubbard, Stephanie M Grasso...

https://pubmed.ncbi.nlm.nih.gov/31390290