Effects of the Combining Physical Exercise and Cognitive Training for the Community-based Elderly
Primary Purpose
Cognitively-normal, Mild Cognitive Impairment, Subjective Cognitive Decline
Status
Not yet recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
perform physical exercise
cognitive training
control group
Sponsored by

About this trial
This is an interventional supportive care trial for Cognitively-normal focused on measuring aerobic exercise, cognitive training
Eligibility Criteria
cognitively-normal elderly
Inclusion Criteria:
- age≥60
- able to follow instruction
- MoCA>26
- not SCD or MCI or Dementia
Exclusion Criteria:
- concomitant neurological conditions such as dementia, Parkinson's disease, brain tumor, brain injury and other brain diseases (such as intracranial hypertension or cerebral edema);
- have unstable cardiovascular status such as uncontrolled hypertension
SCD
Inclusion Criteria:
- age>=60
- SCD(from Ecog-12)
- MoCA≥26
- not MCI or Dementia
Exclusion Criteria:
- concomitant neurological conditions such as dementia, Parkinson's disease, brain tumor, brain injury and other brain diseases (such as intracranial hypertension or cerebral edema);
- have unstable cardiovascular status such as uncontrolled hypertension
MCI
Inclusion Criteria:
(1)age>=60 (2)20 ≦MoCA < 26 (3)MCI (3)not Dementia
Exclusion Criteria:
- concomitant neurological conditions such as dementia, Parkinson's disease, brain tumor, brain injury and other brain diseases (such as intracranial hypertension or cerebral edema);
- have unstable cardiovascular status such as uncontrolled hypertension
Sites / Locations
- Chang Gung Memotial Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
sequential training
simultaneous training
control group
Arm Description
first perform physical exercise followed by cognitive training
perform physical exercise and cognitive tasks simultaneously
perform body stretching and health education courses
Outcomes
Primary Outcome Measures
Change scores of the Montreal Cognitive Assessment (MoCA).
The Montreal Cognitive Assessment (MoCA) will be used to assess general cognitive functions. It examines several cognitive domains with a total score of 30 and higher values indicate better cognitive functions. The MoCA has been shown to be a valid and promising tool to evaluate the global cognitive function in patients with stroke. The psychometric properties of MoCA are good to excellent for patients with cerebrovascular diseases.
Change scores of Wechsler Memory Scale (WMS)
including Faces Recognition (total scale=48), Verbal Paired Associates (total scale = 32), Word Lists (total scale = 48), and Spatial Span (total scale=32) will be used to assess the immediate, delayed, and working memory tests. For each subtest, a higher number indicates better performance in memory function. The raw score of subtests will also be transferred to standardized Z scores and summed to represent an index of general memory function.
Change scores of Stroop test
The participants will be tested under congruent and incongruent conditions. In the congruent condition, the participant will name the color ink of a word which is consistent with the written color name; whereas in the incongruent condition the participant will name the color ink differs from the written color name. The time to complete the task will be calculated for each condition
Change scores of Color trials test
For Part 1, the respondent uses a pencil to rapidly connect circles numbered 1-25 in sequence. For Part 2, the respondent rapidly connects numbered circles in sequence, but alternates between pink and yellow. The length of time to complete each trial is recorded, along with qualitative features of performance indicative of brain dysfunction, such as near-misses, prompts, number sequence errors, and color sequence errors.
Secondary Outcome Measures
Change scores of Verbal fluency tests
Verbal fluency tests are a kind of psychological test in which participants have to produce as many words as possible from a category in a given time (usually 60 seconds).
Change scores of Wechsler Adult Intelligence Scale; WAIS
The digit symbol test involves a key consisting of the numbers 1-9, each paired with a unique, easy-to-draw symbol such as a "V", "+" or ">".
Matrix Reasoning
This is a nonverbal reasoning task in which individuals are asked to identify patterns in designs. This subtest measures:
non-verbal reasoning skills
broad visual intelligence
perceptual organization skills
Change scores of the short (12-item) form of the Everyday Cognition Scale (ECog-12)
The short (12-item) form of the Everyday Cognition Scale (ECog-12), which was developed as an informant-rated report of cognitively mediated functional abilities in older adults. The ECog-12 asks participants to rate their current ability to perform cognitively mediated daily tasks related to everyday memory, language, visuospatial abilities, and executive functions compared with their ability to do the same task 10 years ago. Items are rated on a scale of 1-4, with 1 = Better or no change and 4 = Consistently much worse. The global, executive, and memory ECog-12 sub-domain scores were generated by averaging over the component items (sum of items/number of items) to maintain a range of 1 to 4 (with higher scores reflecting greater self-reported SCD).
Change scores of Dual-task tests
The dual-task test evaluates the ability to shift attention between one task and another. Participants will sit and perform the box and block test (BBT) or walk 10 meters while doing secondary cognitive or motor tasks. Two cognitive secondary tasks will be performed by the participants: (1) arithmetic task: participants will be asked to perform serial subtractions by 7 starting from 100 or random two-digit numbers (e.g., Baetens et al., 2013); (2) tone discrimination task: participants will be presented a number of low and high-pitched tones and they will respond to either the high or low-pitched tones during the trial. Both cognitive task performances will be recorded and the results will be compared to single cognitive task performance. In addition to the cognitive dual-task, participants will perform a motor task (e.g., holding a cup of water) while walking.
Change scores of Six-minute walk test,6MWT
The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance. T
Change scores of Timed up and go (TUG)
The TUG assesses the dynamic balance ability and mobility. The participants will be required to stand up from a chair, walk 3 meters, turn around, walk back to the chair, and sit down. The time to complete the TUG test has been shown to be a good indicator to detect potential fallers in frail elderly (Podsiadlo & Richardson, 1991). The test-retest reliability of TUG on individuals with cognitive impairment was excellent (Blankevoort, van Heuvelen, & Scherder, 2013).
Change scores of 30 second chair stand test,CST
The 30 second sit-to-stand will be assessed to indicate the strength and endurance level of the lower extremities. The participants will be asked to stand up from a standardized chair and then sit down as many times as possible within 30 seconds. The feasibility and reliability of using sit-to-stand test in people with cognitive impairment have been established to be good (Blankevoort et al., 2013).
Change scores of International Physical Activity Questionnaires (IPAQ)
The Chinese version of the International Physical Activity Questionnaires (IPAQ) is an international measure for health-related physical activity. A short form of IPAQ will be used to assess changes in physical activity before and after intervention in this study. The reliability and validity of IPAQ has been established across 12 countries .
The self-report, short-form IPAQ , consists of three questions about days and time of vigorous, moderate, and walking activity in bouts of 10 min, with one question about daily sedentary time in the preceding seven days. The questionnaire was preceded by completion instructions and three questions about the types of vigorous, moderate, and light activity undertaken .
Change scores of Grip strength
The investigator will use hand dynamometer to measure grip strength of both hands while the participant is seated, with the elbow at 90-degree flexion. The investigator will record the mean value of 3 attempts.
Grip strength was measured using a digital dynamometers method, which is a tool with an adjustable grip span, ranging from 3.5 to 7 cm and weighing from 5 to 100 kg with minimal difference around 0.1 kg . All the participants were in a sitting position with fully extended elbows . Then, the investigator measured Grip strength on the dominant hand after 2-3 minutes of resting.
Change scores of short physical performance battery,SPPB
The Short Physical Performance Battery (SPPB) is an objective assessment tool for evaluating lower extremity functioning in older persons. The short physical performance battery (SPPB) is a group of measures that combines the results of the gait speed, chair stand and balance tests . It has been used as a predictive tool for possible disability and can aid in the monitoring of function in older people. The scores range from 0 (worst performance) to 12 (best performance). The SPPB has been shown to have predictive validity showing a gradient of risk for mortality, nursing home admission, and disability.
Change scores of The Clinical Frailty Scale (CFS)
The aim of this scoping review is to identify and document the nature and extent of research evidence related to the Clinical Frailty Scale (CFS). The association of Clinical Frailty Scale (CFS) score with clinical outcomes highlights its utility in the care of the aging population.
The Clinical Frailty Scale (CFS) is a judgement-based frailty tool that evaluates specific domains including comorbidity, function, and cognition to generate a frailty score ranging from 1 (very fit) to 9 (terminally ill).
Change scores of Reported Edmonton Frail Scale (REFS)
Reported Edmonton Frail Scale is an adaptation of Edmonton Frail Scale, that can be performed in less than 10 min by any healthcare professional. Reported Edmonton Frail Scale substitutes the last domain on Edmonton Frail Scale, the physical performance measure, with three self-assessed physical performance questions . This is ideal for use in busy cardiology clinics when patients are being assessed for suitability for intervention.Scoring for the Reported Edmonton Frail Scale range is 0 to18. Not Frail:0-5 ;Apparently Vulnerable:6-7; Mildly Frail:8-9;Moderate Frailty:10-11;Sever Frailty:12-18.
Change scores of Amsterdam Instrumental Activity of Daily Living,A-IADL
The Amsterdam Instrumental Activity of Daily Living (A-IADL) is an adaptive and computerized questionnaire designed to assess impairments in instrumental activities of daily living (IADL) in (early) dementia. The questionnaire is completed by a caregiver, such as a relative or friend.
Each item has a 5-point scale response option (scored 0-4). The scoring of the Amsterdam Instrumental Activity of Daily Living is calculated using item response theory .Lower scores indicating poorer performance.
Change scores of the World Health Organization Quality of Life-Old(WHOQOL-OLD)
The World Health Organization Quality of Life-Old questionnaires demonstrate acceptable psychometric performance in a convenience sample of Taiwan older people. It are valuable measures of Quality of Life-Old for use with older people.Time frame for assessment is the past two weeks.
The items are distributed into 4 domains (physical; psychological, social and environmental health) and 25 facets.
Change scores of Geriatric Depression Scale,GDS
The Geriatric Depression Scale (GDS) is a screening test originally developed by J.A. Yesavage and colleagues in 1982 that is used to identify symptoms of depression in older adults. The scale is a 30-item, self-report instrument that uses a "Yes/No" format.
Change scores of Community Integration Questionnaire, CIQ
The community integration questionnaire (CIQ) was designed to assess home integration, social integration and productive activity in persons with acquired brain injury. The instrument consists of 15 items and can be completed by self report or with the assistance of a family member or caregiver familiar with the person's health status and social activities.
Full Information
NCT ID
NCT05225181
First Posted
January 23, 2022
Last Updated
February 8, 2022
Sponsor
Chang Gung Memorial Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05225181
Brief Title
Effects of the Combining Physical Exercise and Cognitive Training for the Community-based Elderly
Official Title
Effects of the Combining Physical Exercise and Cognitive Training for the Community-based Elderly
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2022 (Anticipated)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chang Gung Memorial Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims to (1) determine the intervention effects of sequential and simultaneous training on cognitive function and health-related function for cognitively-normal elderly and elderly with Mild Cognitive Impairment(MCI) and Subjective Cognitive Decline(SCD); (2) compare which combination approach is more advantageous for improvement on outcome measures.
Detailed Description
The investigators will recruit 30 cognitively-normal elderly and 30 elderly with Mild Cognitive Impairment(MCI) and 30 elderly with Subjective Cognitive Decline(SCD). Participants will be randomly assigned to one of three groups: sequential training (first perform physical exercise followed by cognitive training), simultaneous training (perform physical exercise and cognitive tasks simultaneously), and control group (perform body stretching and health education courses). All participants will receive trainings for 120 minutes per day, one day per week for 12 weeks. The outcome will include measurements that evaluate the cognitive, physical, daily functions, quality of life, and social participation. Participants will be assessed at baseline, after the intervention, and at 3-month follow-up. Repeated measures of analysis of variance (ANOVA) will be used to evaluate the changes in outcome measures at three different time points for the elderly with cognitively-normal, Mild Cognitive Impairment(MCI) and Subjective Cognitive Decline(SCD), respectively. The investigators also use the analysis of covariance (ANCOVA) to investigate the differences between the Mild Cognitive Impairment(MCI) and Subjective Cognitive Decline(SCD) groups on the outcome measures.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitively-normal, Mild Cognitive Impairment, Subjective Cognitive Decline
Keywords
aerobic exercise, cognitive training
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
sequential training
Arm Type
Experimental
Arm Description
first perform physical exercise followed by cognitive training
Arm Title
simultaneous training
Arm Type
Experimental
Arm Description
perform physical exercise and cognitive tasks simultaneously
Arm Title
control group
Arm Type
Active Comparator
Arm Description
perform body stretching and health education courses
Intervention Type
Behavioral
Intervention Name(s)
perform physical exercise
Intervention Description
one 60-min session of physical training
Intervention Type
Behavioral
Intervention Name(s)
cognitive training
Intervention Description
one 60-min session of cognitive training
Intervention Type
Behavioral
Intervention Name(s)
control group
Intervention Description
perform body stretching(15min) and health education courses(90min)
Primary Outcome Measure Information:
Title
Change scores of the Montreal Cognitive Assessment (MoCA).
Description
The Montreal Cognitive Assessment (MoCA) will be used to assess general cognitive functions. It examines several cognitive domains with a total score of 30 and higher values indicate better cognitive functions. The MoCA has been shown to be a valid and promising tool to evaluate the global cognitive function in patients with stroke. The psychometric properties of MoCA are good to excellent for patients with cerebrovascular diseases.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Wechsler Memory Scale (WMS)
Description
including Faces Recognition (total scale=48), Verbal Paired Associates (total scale = 32), Word Lists (total scale = 48), and Spatial Span (total scale=32) will be used to assess the immediate, delayed, and working memory tests. For each subtest, a higher number indicates better performance in memory function. The raw score of subtests will also be transferred to standardized Z scores and summed to represent an index of general memory function.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Stroop test
Description
The participants will be tested under congruent and incongruent conditions. In the congruent condition, the participant will name the color ink of a word which is consistent with the written color name; whereas in the incongruent condition the participant will name the color ink differs from the written color name. The time to complete the task will be calculated for each condition
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Color trials test
Description
For Part 1, the respondent uses a pencil to rapidly connect circles numbered 1-25 in sequence. For Part 2, the respondent rapidly connects numbered circles in sequence, but alternates between pink and yellow. The length of time to complete each trial is recorded, along with qualitative features of performance indicative of brain dysfunction, such as near-misses, prompts, number sequence errors, and color sequence errors.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Secondary Outcome Measure Information:
Title
Change scores of Verbal fluency tests
Description
Verbal fluency tests are a kind of psychological test in which participants have to produce as many words as possible from a category in a given time (usually 60 seconds).
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Wechsler Adult Intelligence Scale; WAIS
Description
The digit symbol test involves a key consisting of the numbers 1-9, each paired with a unique, easy-to-draw symbol such as a "V", "+" or ">".
Matrix Reasoning
This is a nonverbal reasoning task in which individuals are asked to identify patterns in designs. This subtest measures:
non-verbal reasoning skills
broad visual intelligence
perceptual organization skills
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of the short (12-item) form of the Everyday Cognition Scale (ECog-12)
Description
The short (12-item) form of the Everyday Cognition Scale (ECog-12), which was developed as an informant-rated report of cognitively mediated functional abilities in older adults. The ECog-12 asks participants to rate their current ability to perform cognitively mediated daily tasks related to everyday memory, language, visuospatial abilities, and executive functions compared with their ability to do the same task 10 years ago. Items are rated on a scale of 1-4, with 1 = Better or no change and 4 = Consistently much worse. The global, executive, and memory ECog-12 sub-domain scores were generated by averaging over the component items (sum of items/number of items) to maintain a range of 1 to 4 (with higher scores reflecting greater self-reported SCD).
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Dual-task tests
Description
The dual-task test evaluates the ability to shift attention between one task and another. Participants will sit and perform the box and block test (BBT) or walk 10 meters while doing secondary cognitive or motor tasks. Two cognitive secondary tasks will be performed by the participants: (1) arithmetic task: participants will be asked to perform serial subtractions by 7 starting from 100 or random two-digit numbers (e.g., Baetens et al., 2013); (2) tone discrimination task: participants will be presented a number of low and high-pitched tones and they will respond to either the high or low-pitched tones during the trial. Both cognitive task performances will be recorded and the results will be compared to single cognitive task performance. In addition to the cognitive dual-task, participants will perform a motor task (e.g., holding a cup of water) while walking.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Six-minute walk test,6MWT
Description
The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance. T
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Timed up and go (TUG)
Description
The TUG assesses the dynamic balance ability and mobility. The participants will be required to stand up from a chair, walk 3 meters, turn around, walk back to the chair, and sit down. The time to complete the TUG test has been shown to be a good indicator to detect potential fallers in frail elderly (Podsiadlo & Richardson, 1991). The test-retest reliability of TUG on individuals with cognitive impairment was excellent (Blankevoort, van Heuvelen, & Scherder, 2013).
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of 30 second chair stand test,CST
Description
The 30 second sit-to-stand will be assessed to indicate the strength and endurance level of the lower extremities. The participants will be asked to stand up from a standardized chair and then sit down as many times as possible within 30 seconds. The feasibility and reliability of using sit-to-stand test in people with cognitive impairment have been established to be good (Blankevoort et al., 2013).
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of International Physical Activity Questionnaires (IPAQ)
Description
The Chinese version of the International Physical Activity Questionnaires (IPAQ) is an international measure for health-related physical activity. A short form of IPAQ will be used to assess changes in physical activity before and after intervention in this study. The reliability and validity of IPAQ has been established across 12 countries .
The self-report, short-form IPAQ , consists of three questions about days and time of vigorous, moderate, and walking activity in bouts of 10 min, with one question about daily sedentary time in the preceding seven days. The questionnaire was preceded by completion instructions and three questions about the types of vigorous, moderate, and light activity undertaken .
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Grip strength
Description
The investigator will use hand dynamometer to measure grip strength of both hands while the participant is seated, with the elbow at 90-degree flexion. The investigator will record the mean value of 3 attempts.
Grip strength was measured using a digital dynamometers method, which is a tool with an adjustable grip span, ranging from 3.5 to 7 cm and weighing from 5 to 100 kg with minimal difference around 0.1 kg . All the participants were in a sitting position with fully extended elbows . Then, the investigator measured Grip strength on the dominant hand after 2-3 minutes of resting.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of short physical performance battery,SPPB
Description
The Short Physical Performance Battery (SPPB) is an objective assessment tool for evaluating lower extremity functioning in older persons. The short physical performance battery (SPPB) is a group of measures that combines the results of the gait speed, chair stand and balance tests . It has been used as a predictive tool for possible disability and can aid in the monitoring of function in older people. The scores range from 0 (worst performance) to 12 (best performance). The SPPB has been shown to have predictive validity showing a gradient of risk for mortality, nursing home admission, and disability.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of The Clinical Frailty Scale (CFS)
Description
The aim of this scoping review is to identify and document the nature and extent of research evidence related to the Clinical Frailty Scale (CFS). The association of Clinical Frailty Scale (CFS) score with clinical outcomes highlights its utility in the care of the aging population.
The Clinical Frailty Scale (CFS) is a judgement-based frailty tool that evaluates specific domains including comorbidity, function, and cognition to generate a frailty score ranging from 1 (very fit) to 9 (terminally ill).
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Reported Edmonton Frail Scale (REFS)
Description
Reported Edmonton Frail Scale is an adaptation of Edmonton Frail Scale, that can be performed in less than 10 min by any healthcare professional. Reported Edmonton Frail Scale substitutes the last domain on Edmonton Frail Scale, the physical performance measure, with three self-assessed physical performance questions . This is ideal for use in busy cardiology clinics when patients are being assessed for suitability for intervention.Scoring for the Reported Edmonton Frail Scale range is 0 to18. Not Frail:0-5 ;Apparently Vulnerable:6-7; Mildly Frail:8-9;Moderate Frailty:10-11;Sever Frailty:12-18.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Amsterdam Instrumental Activity of Daily Living,A-IADL
Description
The Amsterdam Instrumental Activity of Daily Living (A-IADL) is an adaptive and computerized questionnaire designed to assess impairments in instrumental activities of daily living (IADL) in (early) dementia. The questionnaire is completed by a caregiver, such as a relative or friend.
Each item has a 5-point scale response option (scored 0-4). The scoring of the Amsterdam Instrumental Activity of Daily Living is calculated using item response theory .Lower scores indicating poorer performance.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of the World Health Organization Quality of Life-Old(WHOQOL-OLD)
Description
The World Health Organization Quality of Life-Old questionnaires demonstrate acceptable psychometric performance in a convenience sample of Taiwan older people. It are valuable measures of Quality of Life-Old for use with older people.Time frame for assessment is the past two weeks.
The items are distributed into 4 domains (physical; psychological, social and environmental health) and 25 facets.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Geriatric Depression Scale,GDS
Description
The Geriatric Depression Scale (GDS) is a screening test originally developed by J.A. Yesavage and colleagues in 1982 that is used to identify symptoms of depression in older adults. The scale is a 30-item, self-report instrument that uses a "Yes/No" format.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
Title
Change scores of Community Integration Questionnaire, CIQ
Description
The community integration questionnaire (CIQ) was designed to assess home integration, social integration and productive activity in persons with acquired brain injury. The instrument consists of 15 items and can be completed by self report or with the assistance of a family member or caregiver familiar with the person's health status and social activities.
Time Frame
baseline, after the intervention eight weeks, and at 3-month follow-up.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
cognitively-normal elderly
Inclusion Criteria:
age≥60
able to follow instruction
MoCA>26
not SCD or MCI or Dementia
Exclusion Criteria:
concomitant neurological conditions such as dementia, Parkinson's disease, brain tumor, brain injury and other brain diseases (such as intracranial hypertension or cerebral edema);
have unstable cardiovascular status such as uncontrolled hypertension
SCD
Inclusion Criteria:
age>=60
SCD(from Ecog-12)
MoCA≥26
not MCI or Dementia
Exclusion Criteria:
concomitant neurological conditions such as dementia, Parkinson's disease, brain tumor, brain injury and other brain diseases (such as intracranial hypertension or cerebral edema);
have unstable cardiovascular status such as uncontrolled hypertension
MCI
Inclusion Criteria:
(1)age>=60 (2)20 ≦MoCA < 26 (3)MCI (3)not Dementia
Exclusion Criteria:
concomitant neurological conditions such as dementia, Parkinson's disease, brain tumor, brain injury and other brain diseases (such as intracranial hypertension or cerebral edema);
have unstable cardiovascular status such as uncontrolled hypertension
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ching-yi Wu, ScD
Phone
#886-3-2118800
Ext
5761
Email
cywu@mail.cgu.edu.tw
Facility Information:
Facility Name
Chang Gung Memotial Hospital
City
Taoyuan
ZIP/Postal Code
333
Country
Taiwan
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ching-Yi Wu, ScD
Phone
+886-3-2118800
Ext
5761
Email
cywu@mail.cgu.edu.tw
12. IPD Sharing Statement
Learn more about this trial
Effects of the Combining Physical Exercise and Cognitive Training for the Community-based Elderly
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