TMS in PPA: Transmagnetic Stimulation Pilot in Primary Progressive Aphasia

Sponsor
HealthPartners Institute (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05860647
Collaborator
(none)
3
1
1
7
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Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Device: Intermittent theta burst stimulation
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
3 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Single Arm Study of Resting State Functional Magnetic Resonance Imaging (Rs-fMRI)-Guided Theta Burst Stimulation (TBS) in Primary Progressive Aphasia (PPA)
Anticipated Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intermittent theta burst stimulation

All subjects will receive treatment with intermittent theta burst stimulation (iTBS). There will be a total of 5 treatments over a 2-week period. All subjects will receive iTBS to the right TGd region. TBS treatment will also be provided for two additional sites within the large-scale brain networks (LSBNs) that is found to contain the greatest number of connectivity anomalies. Total participation will be 8-10 weeks.

Device: Intermittent theta burst stimulation
MagVenture TMS Therapy with theta burst stimulation. Resting motor threshold: 80%; Number of pulses per session: 1200 pulses; Inter-train interval: 8 seconds; Pulse frequency in burst: 50 Hertz
Other Names:
  • Transmagnetic stimulation
  • MagVenture
  • Outcome Measures

    Primary Outcome Measures

    1. Connectivity measures of the left TGd, 55b, and STV parcellations at baseline and post-treatment [6 weeks]

      The difference and corresponding 95% confidence interval between follow-up and baseline connectivity measures of the TGd parcellations. Range: -1 to 1. Positive values indicate areas where connectivity is higher than healthy controls from the Human Connectome Project.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Established diagnosis of NFV-PPA and SV-PPA based on criteria (Gorno-Tempini et al.,
    1. Prior brain imaging performed

    2. Mini Mental Status Exam (MMSE)>10

    3. Subjects are between 40-90 years of age

    Exclusion Criteria:
    1. Non-FTD dementia including, but not limited to Alzheimer's, disease, Lewy body dementia, frontotemporal dementia, vascular dementia, Jakob-Creutzfeldt disease, etc.

    2. Inability to tolerate rs-fMRI

    3. Contraindication of rs-fMRI due to implants or metal

    4. Seizure disorder

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 HealthPartners Neuroscience Center Saint Paul Minnesota United States 55130

    Sponsors and Collaborators

    • HealthPartners Institute

    Investigators

    • Principal Investigator: Michael H Rosenbloom, MD, HealthPartners Neurology
    • Principal Investigator: Kashyap Bhavani, PhD,MBBS, HealthPartners Neuroscience Research

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    HealthPartners Institute
    ClinicalTrials.gov Identifier:
    NCT05860647
    Other Study ID Numbers:
    • A23-078
    First Posted:
    May 16, 2023
    Last Update Posted:
    May 19, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by HealthPartners Institute
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 19, 2023