Longitudinal Study to Investigate Different Transcranial Electrical Stimulation (tES)

University of Manitoba

Status: Enrolling

Conditions: Dementia; Degenerative, Dementia Mixed

Treatments: Device: 90 Hz Transcranial Alternating Current Stimulation (tACS); Device: 70 Hz Transcranial Alternating Current Stimulation (tACS); Device: Transcranial Random Noise Stimulation (tRNS); Device: 30 Hz Transcranial Alternating Current Stimulation (tACS); Device: Transcranial Direct Current Stimulation (tDCS); Device: 50 Hz Transcranial Alternating Current Stimulation (tACS)

Study type: Interventional

Funder types: Other

Identifiers

NCT06877312

B2021:089

Details and patient eligibility

About

This research investigates the effect of different frequencies of tACS (0 Hz, 30 Hz, 50 Hz, 70 Hz, 90 Hz) and tRNS with cognitive exercises in a regimen protocol of weeks, everyday. The study design is a longitudinal study design in which participants receive different tES randomly ordered. Treatments occur for 4 weeks, then 12 weeks of no treatment (wash-out period), repeated for each tES treatment type. Participants have the option of having their choice of music in the background while they perform cognitive exercise.

Full description

This research will investigate the effect of applying transcranial electrical stimulation (tES) with different parameters when paired with cognitive exercises with optional background music on older adults in a longitudinal study. In addition, the investigators will investigate and explore novel technological methods not only to monitor the plausible changes due to intervention. Since most technological intervention on dementia have a demanding and costly protocol, it would be of great interest to personalized optimum treatment strategy. The investigators will use Egocentric Spatial Assessment using our Virtual Reality Navigation (VRN) and functional near infrared spectroscopy (fNIRS) measurements and analysis to develop the monitoring technologies. VRN measures how people orient themselves in a non-familiar environment; the investigators hypothesize it is deteriorated significantly in Alzheimer's even at its onset. fNIRS measures oxygenated and deoxygenated blood flow to the brain and it may help to understand neuronal changes due to intervention.

Enrollment: 200 estimated patients

Sex: All

Ages: 50 to 95 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• ability to read, write and speak English fluently
• MoCA score between 5 and 24

Exclusion criteria

• Being diagnosed with Parkinson's, Parkinsonian dementia, Huntington disease, speech significant aphasia and intellectual disability, major depression/anxiety, bipolar disorder, schizophrenia or any other major mood disorder.
• Having a Hhistory of epileptic seizures or epilepsy
• Inability to adequately communicate in English
• Impaired vision or hearing severe enough to impair performance in cognitive tests
• Current substance abuse disorder
• Currently participating in another therapeutic study for dementia
• Plan to change the medication during any treatment period (5 weeks including the pre-post assessments)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: None (Open label)

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200 participants in 6 patient groups

Transcranial Direct Current Stimulation (tDCS)

Experimental group

Description:

Participants will receive active tDCS simultaneously with cognitive exercises. Optional for participants to have their choice of music playing in the background.

Treatment:

Device: Transcranial Direct Current Stimulation (tDCS)

30 Hz Transcranial Alternating Current Stimulation (tACS)

Experimental group

Description:

Participants will receive active tACS at 30 Hz simultaneously with cognitive exercises. Optional for participants to have their choice of music playing in the background.

Treatment:

Device: 30 Hz Transcranial Alternating Current Stimulation (tACS)

50 Hz Transcranial Alternating Current Stimulation (tACS)

Experimental group

Description:

Participants will receive active tACS at 50 Hz simultaneously with cognitive exercises. Optional for participants to have their choice of music playing in the background.

Treatment:

Device: 50 Hz Transcranial Alternating Current Stimulation (tACS)

70 Hz Transcranial Alternating Current Stimulation (tACS)

Experimental group

Description:

Participants will receive active tACS at 70 Hz simultaneously with cognitive exercises. Optional for participants to have their choice of music playing in the background.

Treatment:

Device: 70 Hz Transcranial Alternating Current Stimulation (tACS)

90 Hz Transcranial Alternating Current Stimulation (tACS)

Experimental group

Description:

Participants will receive active tACS at 90 Hz simultaneously with cognitive exercises. Optional for participants to have their choice of music playing in the background.

Treatment:

Device: 90 Hz Transcranial Alternating Current Stimulation (tACS)

Transcranial Random Noise Stimulation (tRNS)

Experimental group

Description:

Participants will receive active tRNS simultaneously with cognitive exercises. Optional for participants to have their choice of music playing in the background.

Treatment:

Device: Transcranial Random Noise Stimulation (tRNS)