UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000061782 |
|---|---|
| Receipt number | R000070702 |
| Scientific Title | Examination of the appropriate stimulation intensity and duration of foam rolling to improve foot flexibility |
| Date of disclosure of the study information | 2026/06/03 |
| Last modified on | 2026/06/03 16:33:28 |
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Basic information
Public title
Examination of the appropriate stimulation intensity and duration of foam rolling to improve foot flexibility
Acronym
Examination of the appropriate protocol for foam rolling aimed at improving foot flexibility
Scientific Title
Examination of the appropriate stimulation intensity and duration of foam rolling to improve foot flexibility
Scientific Title:Acronym
Examination of the appropriate protocol for foam rolling aimed at improving foot flexibility
Region
| Japan |
Condition
Condition
Healthy adult
Classification by specialty
| Orthopedics | Rehabilitation medicine | Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to clarify the appropriate stimulation intensity and duration of foam rolling to improve foot flexibility, and to establish a more effective implementation protocol.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Foot kinematics under load
Key secondary outcomes
Foot morphology
Ground reaction force characteristics during movement
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -but assessor(s) are blinded
Control
Placebo
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
3
Purpose of intervention
Treatment
Type of intervention
| Other |
Interventions/Control_1
Foam rolling on the plantar surface of the feet (low intensity or short duration)
Interventions/Control_2
Foam rolling on the plantar surface of the feet (high intensity or long duration)
Interventions/Control_3
Sham stimulation or medium time
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
| 18 | years-old | <= |
Age-upper limit
| 40 | years-old | > |
Gender
Male and Female
Key inclusion criteria
Those whose foot flexibility falls into the range of normal to rigid.
Key exclusion criteria
Those who have flexible feet.
History of lower limb injury within 3 months prior to participation in the experiment.
History of lower limb surgery.
Pain during walking or running.
Skin diseases of the feet.
Target sample size
23
Research contact person
Name of lead principal investigator
| 1st name | Kazunori |
| Middle name | |
| Last name | Okamura |
Organization
Prefectural University of Hiroshima
Division name
Faculty of Health and Welfare
Zip code
7230053
Address
1-1 Gakuen-cho, Mihara-shi, Hiroshima
TEL
0848601177
k-okamura@pu-hiroshima.ac.jp
Public contact
Name of contact person
| 1st name | Kazunori |
| Middle name | |
| Last name | Okamura |
Organization
Prefectural University of Hiroshima
Division name
Faculty of Health and Welfare
Zip code
723-0053
Address
1-1 Gakuen-cho, Mihara-shi, Hiroshima
TEL
0848601177
Homepage URL
k-okamura@pu-hiroshima.ac.jp
Sponsor or person
Institute
Prefectural University of Hiroshima
Institute
Department
Personal name
Funding Source
Organization
Ministry of education
Organization
Division
Category of Funding Organization
Japanese Governmental office
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
The Ethics Committee of the prefectural university of hiroshima
Address
1-1 Gakuen-cho, Mihara-shi, Hiroshima
Tel
0848-60-1120
k-okamura@pu-hiroshima.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 | 06 | Month | 03 | 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 | 06 | Month | 03 | Day |
Date of IRB
| 2026 | Year | 06 | Month | 01 | Day |
Anticipated trial start date
| 2026 | Year | 06 | Month | 03 | Day |
Last follow-up date
| 2026 | Year | 07 | Month | 31 | 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 | 06 | Month | 03 | Day |
Last modified on
| 2026 | Year | 06 | Month | 03 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000070702
