Tokyo, June 4 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061782) titled 'Examination of the appropriate stimulation intensity and duration of foam rolling to improve foot flexibility' on June 3.
Study Type:
Interventional
Study Design:
Basic Design - Cross-over
Randomization - Randomized
Blinding - Open -but assessor(s) are blinded
Control - Placebo
Primary Sponsor:
Institute - Prefectural University of Hiroshima
Condition:
Condition - Healthy adult
Classification by malignancy - Others
Genomic information - NO
Objective:
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
Intervention:
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)
Eligibility:
Age-lower limit - 18
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 Size - 23
Recruitment Status:
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
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070702
Disclaimer: Curated by HT Syndication.
