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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02480738
Other study ID # 10035434
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2012
Est. completion date July 2013

Study information

Verified date May 2019
Source Seoul National University Bundang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is to investigate the effectiveness of computerized cognitive training, and corresponding neural substrates through multimodal neuroimaging assessment, in the elderly with normal cognition, subjective cognitive impairment, and mild cognitive impairment.


Description:

Computerized cognitive training has the advantage of easy accessibility for community-dwelling elderly. It can be much cheaper than traditional neuropsychological training methods, which require trained neuropsychologists. Furthermore, it may be more fun and easier to be optimized to an individual patients' cognitive status than other traditional methods.

Clinical efficacy of these kinds of cognitive training applications has been validated through several studies. A recent systematic review reported that the domains of working memory, executive function, and processing speed benefited the most by classic computerized cognitive training tasks, and that these benefits were comparable with traditional cognitive training methods. Apart from neuropsychological data, neuroimaging studies focusing on the effectiveness of computerized cognitive training are scant.

There have been no previous studies investigating the possible neural substrates of computerized cognitive training using multimodal neuroimaging modalities simultaneously. Thus, we aimed to investigate the effectiveness of computerized cognitive training and corresponding neural substrates in subjects with mild cognitive impairment, subjective memory impairment, and normal controls through a multimodal approach.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date July 2013
Est. primary completion date April 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 51 Years to 70 Years
Eligibility Inclusion Criteria:

- Ages >50 to =70

- Years of education = 6 years

- No physical barrier preventing the dominant hand from using the computer mouse

Exclusion Criteria:

- Subjects who had any structural lesions or psychiatric disorders that explained the memory deficits

- Subjects had to be able to undergo pre- and post-training evaluations such as electroencephalography (EEG), FDG-PET, and magnetic resonance imaging (MRI)

- Subjects who had scalp lesions, severe back pain, or claustrophobia that precluded pre- and post-training evaluations.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Computerized Cognitive Training Apparatus
CoCoTA was developed through collaborative research with the Korean Institute of Science and Technology (KIST) and Primpo Co. Ltd. (www.primpo.com). It was designed to stimulate numerous cognitive domains simultaneously by using sounds and objects familiar to Korean elderly. Training themes and scenarios were developed and evaluated by six board-certified neurologists and three neuropsychologists who specialize in dementia. Each subject participated in a total of 24 sessions of cognitive training, which consisted of 40 minutes of training, twice per week. To assure the consistency of cognitive training, trained personnel stayed nearby the subjects to help throughout the training process.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Bundang Hospital

References & Publications (1)

Na HR, Lim JS, Kim WJ, Jang JW, Baek MJ, Kim J, Park YH, Park SY, Kim S. Multimodal Assessment of Neural Substrates in Computerized Cognitive Training: A Preliminary Study. J Clin Neurol. 2018 Oct;14(4):454-463. doi: 10.3988/jcn.2018.14.4.454. Epub 2018 J — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical improvement in the follow-up neuropsychological tests changes in memory and frontal domain subscores between the baseline and follow-up 12 weeks
Secondary Cortical thickness changes between baseline and follow-up volumetric MRI surface-based morphometry using freesurfer software 12 weeks
Secondary White matter integrities changes between baseline and follow-up diffusion tensor imaging tract-based spatial statistics using fsl software 12 weeks
Secondary Spectral ratio changes between baseline and follow-up EEG EEG spectral ratio analysis 12 weeks
Secondary local activation pattern changes between baseline and follow-up Fludeoxyglucose PET local activation pattern analysis using SPM 12 weeks
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