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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05384639
Other study ID # 2020.319
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 27, 2021
Est. completion date July 1, 2022

Study information

Verified date May 2022
Source Chinese University of Hong Kong
Contact Raymond Tong, PhD
Phone +85239438454
Email kytong@cuhk.edu.hk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project aims to develop a new dual-task stationary cycling system that can monitor and provide feedback on the aerobic exercise intensity, while administrating appropriate cognitive trainings targeting various cognitive sub domains through a screen in front of the user. The proposed system is designed to train the brain with cognitive tasks and the body with aerobic exercises at the same time. The difficulties of the cognitive tasks are controlled by the users' previous performances on these tasks so that they wouldn't be too easy nor too difficult. Similarly, the intensity of the aerobic exercise will be monitored through an optical encoder for the cycling cadence, two power meters for the force output on the two pedals, as well as a heart rate monitor for the users' physiological response. Constant feedback is being provided to the users so that they will exercise at the correct intensity to provide the greater cardiovascular and cognitive benefits.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date July 1, 2022
Est. primary completion date July 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years to 80 Years
Eligibility Inclusion Criteria: - Clinical diagnosis of MCI or cutoff at 2 < n < 16 th percentile MoCA score according to the level of education and age - Sufficient cognitive ability to follow simple instructions - Able to understand content and purpose of the study - Conscious and in stable physical condition Exclusion Criteria: - Any additional medical or psychological condition that would affect their ability to comply with the study protocol, e.g., a significant orthopaedic or chronic pain condition; or - Severe hip, knee or ankle contracture that would preclude the passive range of motion of the leg - Uncontrolled Cardiac issues

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Dual-task Group
Participant will cycle and perform cognitive training simultaneously.
Cycling Group
Participant will cycle only.
Cognitive Group
Participant will perform cognitive training only.

Locations

Country Name City State
Hong Kong Department of Biomedical Engineering, The Chinese University of Hong Kong Shatin

Sponsors (2)

Lead Sponsor Collaborator
Chinese University of Hong Kong Innovation and Technology Commission, Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary The Montreal Cognitive Assessment, Hong Kong Version (HK-MoCA) Within one month after the last training session
Secondary Trail Making Test Within one month after the last training session
Secondary 6 Minutes Walk Test Within one month after the last training session
Secondary 5 times Sit to Stand Within one month after the last training session
Secondary 10 meters walk Test Within one month after the last training session
Secondary Graded Heart-rate Assessment Within one month after the last training session
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