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NCT05440110Completed

Cognitive Effects of Theta-burst Stimulation (TBS) in Suspected Non-Alzheimer Disease Pathophysiology (SNAP)

Cognitive Effects and Potential Mechanisms of Theta-burst Stimulation (TBS) in Suspected Non-Alzheimer Disease Pathophysiology (SNAP): a Pilot Study

Source: ClinicalTrials.gov · Last updated 23 Mar 2026

Brief summary (registry, in English)

This is a pilot study to identify a homogeneous cohort of pathologically specific dementia with SNAP for clinical trial of brain stimulation.

Status (registry)
Completed
Study type
Interventional
Enrollment
17 (actual)
First submitted
27 Jun 2022
Start date
18 Oct 2022
Primary completion date
15 Aug 2025
Lead sponsor
Chang Gung Memorial Hospital
NCT number
NCT05440110

What you commit to

  • Study type: Interventional
  • Participants enrolled: 17
  • From 18 Oct 2022 to the primary completion date, 15 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any subject has current alcohol or other substances abuse and/ or dependence within the recent one year, or prolonged history of major psychiatric disorder like schizophrenia, bipolar disorder, and previously prolonged substances abuse.
  • General MRI, TMS and/or PET exclusion criteria including subjects who had received brain aneurysm surgery, or implanted pacemaker, mechanical valves, cochlear implant or other metal devices/ objects that are not MR compatible in the body.
    • Withdrawal criteria
  • Use of other therapies or drugs during the intervention period to change cognitive functions.

Other illness

  • Any subject has a definite diagnosis of epilepsy or history of seizure attack.
  • Current or past history of clinically significant neurological insults affecting brain structure or function like completed stroke, head injury or brain tumor. (cerebrovascular disorders, hydrocephalus and intra-cranial mass, documented by MRI; a history of traumatic brain injury or another neurological disease).
  • Any subject has clinically significant or unstable medical diseases including metabolic, renal, liver, lung or cardiovascular disorders including metabolic, renal, liver, lung or cardiovascular disorders.
  • New onset or progression of disease that may affect outcomes.

Other

  • Any females who is pregnant or lactating.
  • Complications onset after intervention that affect efficacy and safety judgments.
  • Any subjects who are recognized as high risk of adverse effects by principle investigator.

Who the study is looking for

  • Subjects aged 50-90 year.
  • Patients meet NIA-AA research criteria for suspected non-Alzheimer disease pathophysiology (SNAP) (Petersen, Smith et al. 1999; Jack, Bennett et al. 2018), and DSM-5 criteria for major neurocognitive disorder of dementia (Regier, Narrow et al. 2013).
  • Amyloid PET should ever be performed.
  • The CDR of subjects can be 0.5-2.

Age in the registry: 50 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chang Gung Memorial Hospital
Coordinator of this site? Confirm its status
TaoyuanTaiwanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.