Therapeutic Efficacy of Categorical Language Fluency Smartphone Game Application
Primary Purpose
Mild Cognitive Impairment, Alzheimer's Disease
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Categorical Language Fluency Smartphone Application
Sponsored by
About this trial
This is an interventional treatment trial for Mild Cognitive Impairment focused on measuring Mild cognitive impairment, Cognitive rehabilitation, Cognitive therapy, Alzheimer's disease, Memory enhancement, Categorical language fluency
Eligibility Criteria
Inclusion Criteria:
- Aged above 55
Confirmed literacy
- Diagnosed to mild cognitive impairment by International Working Group on Mild Cognitive Impairment and Clinical Dementia Rating(CDR) of 0 or 0.5.
- Diagnosed to possible or probable Alzheimer's dementia by NINCDS-ADRDA and Clinical Dementia Rating(CDR) of 1 or below.
Exclusion Criteria:
- Evidence of delirium, confusion
- Any neurological conditions causing cognitive decline such as Parkinson's disease, brain hemorrhage, brain tumor, normal pressure hydrocephalus
- Evidence of severe cerebrovascular pathology
- History of loss-of-consciousness over 1 hour due to head trauma or repetitive head trauma of mild severity
- History of substance abuse or dependence such as alcohol
- Presence of depressive symptoms that could influence cognitive function
- Presence of medical comorbidities that could result in cognitive decline
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Categorical Language Fluency Smartphone Application
Arm Description
Smartphone game application specifically aimed at training categorical language fluency
Outcomes
Primary Outcome Measures
Application usage log
Log to assess compliance of participant(by describing frequency and duration of training by using application)
Secondary Outcome Measures
Subjective Memory Complaint Questionnaire
to evaluate efficacy of application
Geriatric Depression Scale
to evaluate efficacy of application
Korean version of MMSE for dementia screening
to evaluate efficacy of application
Full Information
NCT ID
NCT02848404
First Posted
July 20, 2016
Last Updated
March 23, 2020
Sponsor
Seoul National University Bundang Hospital
Collaborators
Seoul National University, Ministry of Science, ICT and Future Planning
1. Study Identification
Unique Protocol Identification Number
NCT02848404
Brief Title
Therapeutic Efficacy of Categorical Language Fluency Smartphone Game Application
Official Title
A Study of Therapeutic Efficacy of Categorical Language Fluency Smartphone Game Application in Mild Cognitive Impairment and Mild Alzheimer's Dementia (Baseline Study)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
June 2016 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
February 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Bundang Hospital
Collaborators
Seoul National University, Ministry of Science, ICT and Future Planning
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to examine therapeutic efficacy of categorical language fluency smartphone game application in mild cognitive impairment and mild Alzheimer's dementia.
Detailed Description
The Categorical Language Fluency Smartphone Game Application was developed based on the semantic distance training, which was effective in improving categorical language fluency of mild cognitive impairment and mild Alzheimer's dementia. 10 patients with mild cognitive impairment and another 10 patients with mild Alzheimer's dementia were recruited to examine therapeutic efficacy of the application.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Cognitive Impairment, Alzheimer's Disease
Keywords
Mild cognitive impairment, Cognitive rehabilitation, Cognitive therapy, Alzheimer's disease, Memory enhancement, Categorical language fluency
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Categorical Language Fluency Smartphone Application
Arm Type
Experimental
Arm Description
Smartphone game application specifically aimed at training categorical language fluency
Intervention Type
Device
Intervention Name(s)
Categorical Language Fluency Smartphone Application
Intervention Description
4 weeks' training
Primary Outcome Measure Information:
Title
Application usage log
Description
Log to assess compliance of participant(by describing frequency and duration of training by using application)
Time Frame
4-weeks treatment
Secondary Outcome Measure Information:
Title
Subjective Memory Complaint Questionnaire
Description
to evaluate efficacy of application
Time Frame
after 4-weeks treatment
Title
Geriatric Depression Scale
Description
to evaluate efficacy of application
Time Frame
after 4-weeks treatment
Title
Korean version of MMSE for dementia screening
Description
to evaluate efficacy of application
Time Frame
after 4-weeks treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged above 55
Confirmed literacy
Diagnosed to mild cognitive impairment by International Working Group on Mild Cognitive Impairment and Clinical Dementia Rating(CDR) of 0 or 0.5.
Diagnosed to possible or probable Alzheimer's dementia by NINCDS-ADRDA and Clinical Dementia Rating(CDR) of 1 or below.
Exclusion Criteria:
Evidence of delirium, confusion
Any neurological conditions causing cognitive decline such as Parkinson's disease, brain hemorrhage, brain tumor, normal pressure hydrocephalus
Evidence of severe cerebrovascular pathology
History of loss-of-consciousness over 1 hour due to head trauma or repetitive head trauma of mild severity
History of substance abuse or dependence such as alcohol
Presence of depressive symptoms that could influence cognitive function
Presence of medical comorbidities that could result in cognitive decline
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ki Woong Kim, M.D., Ph.D.
Organizational Affiliation
Seoul National University Bundang Hospital, Seong-nam, Korea
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Therapeutic Efficacy of Categorical Language Fluency Smartphone Game Application
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