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NCT06563453Completed

Implication of Cognitive Reserve in Non-pharmacological Intervention Outcomes

Source: ClinicalTrials.gov · Last updated 16 Oct 2026

Brief summary (registry, in English)

Cognitive reserve (CR) is defined as the gradual accumulation of neural resources and their adaptability (i.e., efficiency, capacity, flexibility) due to genetic and/or lifelong environmental factors that mitigate the cognitive effects of age-related processes and brain diseases. Transcranial alternating current stimulation (tACS) can be used to entrain underlying neuronal networks, promoting firing at specific frequencies. Recent studies have demonstrated that fronto-parietal theta oscillatory activity entrainment via tACS leads to working memory enhancement in healthy subjects. However, there remains significant variability in stimulation-induced aftereffects across individuals. Emerging literature suggests that individual differences, such as CR levels, may be crucial in predicting the benefits of treatment interventions, as they reflect available neural capacity and flexibility. A novel interventional approach is proposed to study CR, utilizing both conventional static proxies, such as premorbid intellect and educational attainment, and dynamic markers, including pupillometry, resting-state, and task-induced functional MRI. By employing cutting-edge noninvasive brain stimulation (NIBS) techniques, the study will acutely modulate network properties to examine the influence of CR on immediate cognitive and brain functional aftereffects induced by the intervention. In addition to focusing on cognitively healthy older adults, this study will, for the first time, include patients with mild cognitive impairment with Lewy bodies (MCI-LB), a prodromal stage of the second most common degenerative dementia after Alzheimer's disease.

Status (registry)
Completed
Study type
Interventional
Enrollment
55 (actual)
First submitted
19 Aug 2024
Start date
18 Jun 2022
Primary completion date
30 Aug 2024
Lead sponsor
Masaryk University
NCT number
NCT06563453

What you commit to

  • Study type: Interventional
  • Participants enrolled: 55
  • From 18 Jun 2022 to the primary completion date, 30 Aug 2024
  • 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.

Other illness

  • Presence of dementia as assessed by a cognitive test battery and evaluation of daily activities.
  • Any major psychiatric disorder.
  • History of neurological disease affecting the central nervous system (e.g., tumor, epilepsy, stroke, etc.).
  • Non-compensated internal or oncological disease. MRI-incompatible metal in the body (e.g., pacemaker). Left-handedness.

Other

  • Severe or repeated head injury.

Who the study is looking for

  • Intact cognitive performance as assessed by cognitive evaluation.
  • Subjects with possible or probable mild cognitive impairment with Lewy bodies (MCI-LB).

Age in the registry: 60 years to 75 years · Sex: All · Accepts 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
CEITEC Masaryk University
Coordinator of this site? Confirm its status
BrnoCzechiaUnknown status

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