UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000062940 |
|---|---|
| Receipt number | R000072058 |
| Scientific Title | Effects of dual-task training combining face-to-face and online delivery in community-dwelling older adults: a randomised crossover trial |
| Date of disclosure of the study information | 2026/09/27 |
| Last modified on | 2026/09/20 12:46:59 |
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Basic information
Public title
Effects of dual-task training combining face-to-face and online delivery in community-dwelling older adults: a randomised crossover trial
Acronym
Effects of dual-task training combining face-to-face and online delivery in community-dwelling older adults: a randomised crossover trial
Scientific Title
Effects of dual-task training combining face-to-face and online delivery in community-dwelling older adults: a randomised crossover trial
Scientific Title:Acronym
Effects of dual-task training combining face-to-face and online delivery in community-dwelling older adults: a randomised crossover trial
Region
| Japan |
Condition
Condition
Community-dwelling older adults
Classification by specialty
| Not applicable | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To investigate the effects of dual-task training combining face-to-face and online delivery in community-dwelling older adults
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Dual-task performance (Dual-task Timed Up and Go test)
Key secondary outcomes
Attentional function (Trail making test Japanese: TMT-J)
General cognition (The Japanese version of the Montreal Cognitive Assessment: MoCA-J)
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -but assessor(s) are blinded
Control
No treatment
Stratification
YES
Dynamic allocation
Institution consideration
Blocking
YES
Concealment
Intervention
No. of arms
2
Purpose of intervention
Prevention
Type of intervention
| Behavior,custom |
Interventions/Control_1
Participants will receive dual-task training combining face-to-face and online delivery for 1 hour per session, twice a week for 4 weeks.
Interventions/Control_2
Participants continue their usual daily life for 4 weeks.
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| 65 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
(1) individuals aged 65 years and over
(2) individuals who understand the study and are able to provide informed consent to participate voluntarily.
Key exclusion criteria
(1) individuals who have been advised by a physician to restrict exercise, including those with conditions such as severe hypertension, cardiac diseases, or undergoing treatment for fractures that require exercise limitation
(2) individuals with cognitive impairment that the principal investigator considers would make participation in the study difficult.
Target sample size
60
Research contact person
Name of lead principal investigator
| 1st name | Maki |
| Middle name | |
| Last name | Ogasawara |
Organization
Fukushima Medical University
Division name
Department of Occupational Therapy, School of Health Sciences
Zip code
960-8516
Address
10-6 Sakaemachi, Fukushima City, Fukushima
TEL
024(581)5553
oga-maki@fmu.ac.jp
Public contact
Name of contact person
| 1st name | Maki |
| Middle name | |
| Last name | Ogasawara |
Organization
Fukushima Medical University
Division name
Department of Occupational Therapy, School of Health Sciences
Zip code
960-8516
Address
10-6 Sakaemachi, Fukushima City, Fukushima
TEL
024(581)5553
Homepage URL
oga-maki@fmu.ac.jp
Sponsor or person
Institute
Fukushima Medical University
Institute
Department
Personal name
Funding Source
Organization
Japan Society for the Promotion of Science
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Japan
Other related organizations
Co-sponsor
Name of secondary funder(s)
Kagamiishi Town
IRB Contact (For public release)
Organization
Fukushima Medical University General Ethics Committee
Address
1 Hikariga-oka, Fukushima City, Fukushima
Tel
024(547)1825
fmurec@fmu.ac.jp
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 09 | Month | 27 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Preinitiation
Date of protocol fixation
| 2026 | Year | 05 | Month | 28 | Day |
Date of IRB
| 2026 | Year | 09 | Month | 15 | Day |
Anticipated trial start date
| 2026 | Year | 10 | Month | 01 | Day |
Last follow-up date
| 2026 | Year | 11 | Month | 27 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2026 | Year | 09 | Month | 16 | Day |
Last modified on
| 2026 | Year | 09 | Month | 20 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000072058
