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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03839563
Other study ID # NHRI-EX108-10804PI
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 15, 2019
Est. completion date December 31, 2023

Study information

Verified date September 2022
Source Taipei Medical University
Contact Mau-Roung Lin, Professor
Phone 886-2-27361661
Email mrlin@tmu.edu.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The effectiveness of conventional exercise, tai chi chuan and health education/usual physical activity over a 6-month intervention period in improving primary outcomes and secondary outcomes in older mild cognitive impairment adults will be compared. Third, whether changes in serum levels of the brain-derived neurotrophic factor (BDNF), insulin-like growth factor (IGF)-1, and vascular endothelial growth factor (VEGF) and expression of the apolipoprotein E (APOE) ε4 allele parallel changes in gait characteristics and cognitive functions after the intervention will be examined.


Recruitment information / eligibility

Status Recruiting
Enrollment 189
Est. completion date December 31, 2023
Est. primary completion date December 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years to 100 Years
Eligibility Inclusion Criteria: - At least 65 years old - Had an emergency department visit due to a fall at least 3 months prior to the baseline assessment (assuming a full recovery time from a fall to be 3 months) - Can ambulate independently - Has mild cognitive impairment Exclusion Criteria: - Do not live in a community setting - Cannot ambulate independently and communicate with researchers - Have a major unstable cardiopulmonary disease (e.g., ischemic chest pain, shortness of breath, recurrent syncopal episodes, orthopnea, paroxysmal nocturnal dyspnea, palpitations, or tachycardia) - Have a contraindication to physical exercise (e.g., severe osteoarthritis or severe pulmonary hypertension)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Exercise
Each session will last 60 min, consisting of 10 min of warm-up, 45 min of exercise, and a 5-min cool-down.

Locations

Country Name City State
Taiwan Taipei Medical University Taipei

Sponsors (2)

Lead Sponsor Collaborator
Taipei Medical University National Health Research Institutes, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gait characteristics Performance on six gait characteristics (velocity, cadence, stride length, swing time, stride length variability, and swing time variability) will be measured with a 6-m electronic walkway of GAITRite. 12 months
Primary Global cognition Global cognition will be assessed using the Mini-Mental State Examination (MMSE). The MMSE comprises 11 questions, and the score ranges 0~30, with lower scores indicating poorer global cognition. 12 months
Primary Serum levels of BDNF Serum BDNF concentrations will be assessed. 12 months
Primary Serum levels of IGF-1 Serum IGF-1 concentrations will be assessed. 12 months
Primary Serum levels of VEGF Serum VEGF concentrations will be assessed. 12 months
Secondary Tinetti balance The Tinetti balance score ranges 0~26, with a higher score indicating a better balance ability. 12 months
Secondary Mobility The timed up and go test requires subjects to rise from a standard chair, walk a distance of 3 m, turn, walk back to the chair, and sit down. The time to complete the timed up and go will be recorded. 12 months
Secondary Muscle strength Grip strength will be assessed via a handgrip dynamometer and measured in kilograms of isometric force. 12 months
Secondary Falls number of falls and multiple falls 12 months
Secondary Depressive symptoms Depressive symptoms will be assessed using the 15-item Geriatric Depression Scale (GDS). 12 months
Secondary Fear of falling Fear of falling will be assessed using the Falls Efficacy Scale (FES) test. 12 months
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