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N/A N=3 Treatment

Transmagnetic Stimulation Pilot in Primary Progressive Aphasia

Primary Progressive Aphasia

Enrolled (actual)
3
Serious AEs
0.0%
Results posted
Jun 2025
Primary outcome: Primary: Connectivity Measures of the Left TGd, 55b, and STV Parcellations at Baseline and Post-treatment — -.06; .03; -.01 correlation

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Intermittent theta burst stimulation (Device)
Age
Adult, Older Adult · 40+ yrs
Sex
All
Sponsor
HealthPartners Institute
Primary completion
May 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Connectivity Measures of the Left TGd, 55b, and STV Parcellations at Baseline and Post-treatment
-.06; .03; -.01

Summary

Frontotemporal degeneration (FTD) is a non-Alzheimer's dementia that is the 2nd most common cause of dementia in the United States. FTD may present with focal language symptoms that are clinically described as primary progressive aphasia (PPA). There are two types of PPA associated with FTD-semantic variant primary progressive aphasia (SV-PPA) and nonfluent/agrammatic variant primary progressive aphasia (NFV-PPA). Both diseases are progressive neurodegenerative disease processes that compromise dominant hemisphere large scale brain network function, ultimately resulting in mutism. There are currently no FDA-approved treatments for PPA and management is mostly supportive. In combination with resting state functional MRI (rs-fMRI), transcranial magnetic stimulation (TMS) with intermittent theta burst stimulation (iTBS) offers a non-invasive alternative to pharmacotherapy in persons with PPA. In our prior studies of Alzheimer's disease (AD) and Lewy body Dementia (LBD) subjects, investigators have determined that the anterior temporal pole (area TGd and TGv) is an area that is commonly dysfunctional in dementia. The investigators have already embarked upon an fMRI guided study of iTBS in early stage Alzheimer's disease where subjects received a series of 5 treatments to distinct brain regions inclusive of area TGd. The investigators propose a case study of 3 PPA studies where rs-fMRI is applied to the large-scale language networks.

Eligibility Criteria

Inclusion Criteria

  • Established diagnosis of NFV-PPA and SV-PPA based on criteria (Gorno-Tempini et al., 2011)
  • Prior brain imaging performed
  • Mini Mental Status Exam (MMSE)>10
  • Subjects are between 40-90 years of age

Exclusion Criteria

  • Non-FTD dementia including, but not limited to Alzheimer's, disease, Lewy body dementia, frontotemporal dementia, vascular dementia, Jakob-Creutzfeldt disease, etc.
  • Inability to tolerate rs-fMRI
  • Contraindication of rs-fMRI due to implants or metal
  • Seizure disorder
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05860647). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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