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Clinical Trials/NCT04555941
NCT04555941
Completed
Phase 2

Cognitive Effects of Theta Burst Stimulation in Mild Cognitive Impairment and Alzheimer's Disease

Taipei Medical University Shuang Ho Hospital1 site in 1 country54 target enrollmentOctober 5, 2020

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Mild Cognitive Impairment
Sponsor
Taipei Medical University Shuang Ho Hospital
Enrollment
54
Locations
1
Primary Endpoint
Changes from baseline in scores of any tests of the Neuropsychological Battery
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Transcranial magnetic stimulation (TMS) is a noninvasive brain stimulation technique that is increasingly used for a growing number of research and clinical applications.Typically, this transient magnetic field is focally applied with a figure-of-eight coil that is carefully placed on the surface of the scalp over a targeted stimulation site. Patterned repetitive TMS (rTMS), such as theta burst stimulation (TBS) can produce long-lasting effects on neural activity and behavior beyond the stimulation period (Chou et al., 2015a; Fitzgerald et al., 2006). In general, high frequency (> 5 Hz) rTMS and its newer version, intermittent theta burst stimulation (iTBS), facilitate cortical excitability, whereas low frequency (about 1 Hz) rTMS and continuous theta burst stimulation contribute to opposite effects (Pascual-Leone et al., 2000; Huang et al., 2005; Wassermann and Zimmermann, 2012).Careful manipulation of the parameters comprising these patterned rTMS pulse trains can induce neuroplastic changes that resemble either long-term potentiation (LTP) or depression (Chen et al., 1997; Pascual-Leone et al., 1994). Early studies targeting the motor cortex helped elucidate which rTMS parameters promote particular responses and their neurophysiological underpinnings (Klomjai et al., 2015).

In recent years, rTMS has been closely investigated to evaluate its potential to modulate cognitive functions in Alzheimer'sdisease (AD) and mild cognitive impairment (MCI). As compared to conventional excitatory rTMS protocols, iTBS leads to comparable effects with similar number of pulses but considerable shorter duration and lower intensity of stimulation (Bakker et al., 2015; Rossi, Hallett, Rossini, Pascual-Leone, & Safety, 2009). Recent literature also suggest that TBS has lower rates of reported adverse event (AE) compared to rTMS (Najib & Horvath, 2014). Therefore, iTBS is assumed to modulate cognitive function in people with cognitive impairments.

Detailed Description

Visit 1: Informed Consent, Brain MRI/Neuropsychological Battery Visit 2-11: (up to a week after visit 1) iTBS - or Sham-Treatment (10 sessions, 80% Resting Motor Threshold, 2s stimulation 8s inter-stimulus interval per train, 20 trains per block, 3 blocks per session with a 5-min break, 1 session per day) Visit 12: (1 day or same day after visit 11) Functional Brain MRI/Neuropsychological Battery Visit 13: (4 weeks after visit 11) Functional Brain MRI/Neuropsychological Battery

Registry
clinicaltrials.gov
Start Date
October 5, 2020
End Date
January 31, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Taipei Medical University Shuang Ho Hospital
Responsible Party
Principal Investigator
Principal Investigator

Cheng-Chang Yang

Medical researcher

Taipei Medical University Shuang Ho Hospital

Eligibility Criteria

Inclusion Criteria

  • normal visual acuity
  • diagnosed with mild cognitive impairment or early dementia due to Alzheimer's disease (CDR = 0.5) by neurologists

Exclusion Criteria

  • (family) history of seizure attacks
  • in intensive care
  • history of drug/alcohol dependence
  • assistants or students of the PI
  • major systemic diseases concerning cognitive decline (e.g., cardiopulmonary failure, liver/renal failure, poor controlled DM, traumatic brain injury, stroke, or other neurodegenerative diseases)
  • claustrophobia
  • metal implants
  • taking medication lowering the threshold of seizure attacks
  • fear of using TMS
  • with specific allergens

Outcomes

Primary Outcomes

Changes from baseline in scores of any tests of the Neuropsychological Battery

Time Frame: Baseline, immediate post-iTBS, follow-up (4 weeks post-iTBS)

WAIS-IV short-form, Word Sequence Learning Test, Benton Visual Retention Test, Color Trial Tests, 3-D Dimensional Constructional Test, Visual Confrontation Naming, Semantic Verbal Fluency Test, Stroop Color-Word Test

Secondary Outcomes

  • Brain MRI(Baseline, immediate post-iTBS, follow-up (4 weeks post-iTBS))

Study Sites (1)

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