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Enrolling by invitation NCT05967390

Localized Analysis of Normalized Distance From Scalp to Cortex and Personalized Evaluation (LANDSCAPE)

Observational Aging Dementia Alzheimers Parkinson Disease Dementia Frontotemporal

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Transcranial Magnetic Stimulation.
Who it may be relevant to
Registry conditions: Aging, Dementia Alzheimers, Parkinson Disease, Dementia Frontotemporal. Basic parameters: 60 years — 95 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Hong Kong
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Localized Analysis of Normalized Distance From Scalp to Cortex and Personalized Evaluation (LANDSCAPE): A Project of MRI-informed Computational Head Model

Overview

Scalp to cortex distance (SCD), as a key technological parameter of brain stimulation, has been highlighted in the guidelines of non-invasive brain stimulation. However, in the context of age-related brain changes, the region-specific SCD and its impact on stimulation-induced electric field in different types of neurodegenerative diseases remain unclear.

Detailed description

Objective: This study aimed to investigate the region-specific SCD and its relationship with morphometric features and cognitive function in age- and disease-specific populations. Methods: The SCD and cortical thickness (CT) of left primary motor cortex (M1) and dorsolateral prefrontal cortex (DLPFC) were measured in cognitively normal adults and dementia patients. CT-adjusted SCD was used to control the influence of CT on SCD. Head model was developed to simulate the impact of SCD on the electric field induced by transcranial electrical stimulation.

Interventions

  • Device Transcranial Magnetic Stimulation
    One time for each day, lasting for three weeks.

Primary outcome measures

  • Scalp-to-cortex distance will be measured using geometric brain model [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Right-handed as assessed by the Edinburgh Inventory
  • Able to attend TMS interventions
  • Consent
  • Independent in daily life activities

Exclusion criteria

  • Uncorrected visual or auditive deficits not allowing the realization of the test
  • Evolutive disease (such as cancer)
  • Neurological or psychiatric antecedent
  • Counter-indication to MRI

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

Hong Kong · 1 center
  • Tai Po Hospital — Hong Kong

Identifiers

NCT: NCT05967390 · 2018.077 · 2018.077

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗