Effects of Combined 40 Hz Audio-visual Stimulation and Cognitive Games on Alzheimer's Disease

NCT ID: NCT06595511

Last Updated: 2024-09-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-10-01

Study Completion Date

2025-04-30

Brief Summary

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In addition to ongoing drug treatments for Alzheimer Disease (AD), protective approaches that can halt the progression of the disease are of particular importance. This project aims to develop a digital application that can monitor cognitive impairment, using EEG findings proven effective at the clinical level in Alzheimer and various types of dementia, including sensory entrainment and digital cognitive games.

To this end, a collaboration between Istanbul Medipol University and Güven Future Health Technologies Inc. will develop a device featuring audio-visual sensory entrainment and digital cognitive games. This device will be made available to Alzheimer patients, and the differences between patients who use the application for three months, patients who do not use the application, and healthy controls will be evaluated through neurological examinations, neuropsychological tests, and EEG recordings indicating cognitive functions by the neurologist, project coordinator, and bursars. Monthly assessments, including EEG recordings, will also continue at home, and an application will be created to evaluate changes in cognitive functions through EEG data.

By the end of the project, an application that includes sensory entrainment and digital cognitive games, proven effective at the clinical level using EEG findings for Alzheimer dementia patients, will be developed. Additionally, a health kit capable of temporal monitoring of cognitive function changes through EEG data will have been developed.

Detailed Description

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This study aims to recruit early and middle-stage Alzheimer patients aged between 60 and 75, along with age and gender-matched healthy older adults. Two different Alzheimer groups will be created: one group will utilize a 40 Hz sensory entrainment-integrated cognitive game kit at home, while the other group will not receive any treatment. The treatment group will comprise 10 Alzheimer patients who will engage with the 40 Hz sensory entrainment-integrated cognitive game kit for 1 hour a day, at least five days a week, for three months. Comprehensive neuropsychological assessments and electroencephalography (EEG) recordings will be conducted in the laboratory on the first day, followed by mobile EEG recordings at home at the end of the first and second months. After three months of using the sensory entrainment/cognitive game kit, the participants will again undergo neuropsychological assessment and EEG recording in the laboratory. The second Alzheimer group (n=10) will not be administered any treatment and will undergo the same assessment protocol as the treatment group. Furthermore, in addition to these two groups, a healthy older adult group (n=10) will also be included in the study, with assessments scheduled only on the first day and at the end of the third month.

Conditions

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Alzheimer's Disease 40 Hz Stimulation EEG Brain Oscillations

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Alzheimer's Disease Treatment Group

The group will engage with the 40 Hz sensory entrainment-integrated cognitive game kit for one hour a day, five days a week, for three months.

Group Type ACTIVE_COMPARATOR

Sensory Entrainment-Integrated Cognitive Game Kit

Intervention Type DEVICE

Active comparator group will engage with the 40 Hz sensory entrainment-integrated cognitive game kit for one hour a day, at least five days a week, for three months.

Alzheimer's Disease Control Group

Group Type NO_INTERVENTION

No interventions assigned to this group

Healthy Older Adult Group

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Sensory Entrainment-Integrated Cognitive Game Kit

Active comparator group will engage with the 40 Hz sensory entrainment-integrated cognitive game kit for one hour a day, at least five days a week, for three months.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Diagnosed with AD according to DSM-IV and NINCDS-ADRDA criteria,
* Impaired activities of daily living,
* Having a CDR score of 1-2 and an SMMT score of 15-26,
* Stable use of psychoactive medications, including acetylcholinesterase inhibitors or other medications that enhance cognitive functions,
* Individuals aged 60-86 with at least 5 years of education.


* Between the ages of 60-86
* Without any neurological abnormalities or general cognitive impairment (MMSE above 25),
* Not diagnosed with a neurological and/or psychiatric disease,
* Not using neurological and/or psychiatric medication

Exclusion Criteria

* Having frontotemporal dementia, vascular dementia, Lewy body dementia or other types of dementia,
* Parkinsonism, clinical depression, other mental disorders, epilepsy, drug addiction, alcohol addiction, and traumatic brain injury



* Having clinical signs of cognitive impairment, such as mild cognitive impairment, Alzheimer disease, Parkinson disease, Lewy body dementia, frontotemporal dementia, etc.
* Epilepsy, alcohol and/or drug addiction, use of medications that affect cognitive functions, and traumatic brain injury
Minimum Eligible Age

60 Years

Maximum Eligible Age

86 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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The Scientific and Technological Research Council of Turkey

OTHER

Sponsor Role collaborator

Guven Health Group

OTHER

Sponsor Role collaborator

Istanbul Medipol University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Bahar Güntekin

Prof. Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Istanbul Medipol University

Istanbul, Beykoz, Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Bahar Güntekin, PhD

Role: CONTACT

+90 5326031560

Facility Contacts

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Bahar Güntekin, PhD

Role: primary

+90 5326031560

Other Identifiers

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E-10840098-772.02-6692

Identifier Type: -

Identifier Source: org_study_id

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