- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Forventet)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Raymond Tong, PhD
- Telefonnummer: +85239438454
- E-post: kytong@cuhk.edu.hk
Studiesteder
-
-
-
Shatin, Hong Kong
- Rekruttering
- Department of Biomedical Engineering, The Chinese University of Hong Kong
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
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 studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Dual-task Group
|
Participant will cycle and perform cognitive training simultaneously.
|
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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.
|
Hva måler studien?
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
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Raymond Tong, PhD, Department of Biomedical Engineering, The Chinese University of Hong Kong
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2020.319
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
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