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40Hz tACS in Treating Cognitive Function and Modulating Neurophysiology of Patients With Alzheimer's Disease

C

Che-Sheng Chu

Status

Enrolling

Conditions

Alzheimer Disease

Treatments

Device: sham tACS
Device: active tACS

Study type

Interventional

Funder types

Other

Identifiers

NCT05723172
VGHKS-112-01

Details and patient eligibility

About

Gamma brain activity is crucial for cognitive function and intra-brain communication. Gamma frequency stimulation via transcranial alternating current stimulation(tACS) might alleviate memory deficits on both animal models of Alzheimer's disease (AD) and clinical trial. The study aims to assess the safety and efficacy of tACS on cognitive function and modulating neurophysiology in patients with AD.

Full description

Gamma brain activity is crucial for cognitive function and intra-brain communication. Gamma frequency stimulation via transcranial alternating current stimulation(tACS) might alleviate memory deficits on both animal models of Alzheimer's disease (AD) and clinical trial. The study aims to assess the safety and efficacy of tACS on cognitive function and modulating neurophysiology in patients with AD.

40mins 10Hz-tACS for daily consecutive sessions will be given.

Enrollment

48 estimated patients

Sex

All

Ages

60 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged 60- to 90-year-old
  • clinical dementia rating scale (CDR) of 1 or mini-mental state examination (MMSE) score of 18 to 26.
  • Participants were allowed to maintain their anti-dementia medications without changes from at 3 months before and throughout the study.

Exclusion criteria

  • having contraindications for tACS, e.g., implanted brain medical devices or mental in the head, having arrhythmia and with pacemaker implantation, having history of seizures, having history of intracranial neoplasms or surgery, or severe head injuries or cerebrovascular diseases
  • clinical depression measured by Hamilton depression rating scale score equal and over 17

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

48 participants in 2 patient groups

active tACS
Active Comparator group
Description:
40 mins tACS for 10 consecutive daily sessions
Treatment:
Device: active tACS
sham tACS
Sham Comparator group
Description:
40 mins sham tACS for 10 consecutive daily sessions
Treatment:
Device: sham tACS

Trial contacts and locations

1

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Central trial contact

Che-Sheng Chu

Data sourced from clinicaltrials.gov

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