- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05384639
Dual-task Cycling System on Cognitive Function for the Elderly
Simultaneous Dual-Task Cycling Exercise Training on Cognitive Function for the Elderly
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.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
- Navn: Raymond Tong, PhD
- Telefonnummer: +85239438454
- E-mail: kytong@cuhk.edu.hk
Studiesteder
-
-
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Shatin, Hong Kong
- Rekruttering
- Department of Biomedical Engineering, The Chinese University of Hong Kong
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
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
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Dual-task Group
|
Participant will cycle and perform cognitive training simultaneously.
|
Aktiv komparator: Cycling Group
|
Participant will cycle only.
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Aktiv komparator: Cognitive Group
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Participant will perform cognitive training only.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
The Montreal Cognitive Assessment, Hong Kong Version (HK-MoCA)
Tidsramme: Within one month after the last training session
|
Within one month after the last training session
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Trail Making Test
Tidsramme: Within one month after the last training session
|
Within one month after the last training session
|
6 Minutes Walk Test
Tidsramme: Within one month after the last training session
|
Within one month after the last training session
|
5 times Sit to Stand
Tidsramme: Within one month after the last training session
|
Within one month after the last training session
|
10 meters walk Test
Tidsramme: Within one month after the last training session
|
Within one month after the last training session
|
Graded Heart-rate Assessment
Tidsramme: Within one month after the last training session
|
Within one month after the last training session
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Raymond Tong, PhD, Department of Biomedical Engineering, The Chinese University of Hong Kong
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2020.319
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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