Tokyo, June 16 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061910) titled 'Effects of Functional Recovery Wear on Recovery After High-Load Exercise' on June 16.
Study Type:
Interventional
Study Design:
Basic Design - Cross-over
Randomization - Randomized
Blinding - Double blind -all involved are blinded
Control - Placebo
Primary Sponsor:
Institute - EUPHORIA Co., Ltd.
Condition:
Condition - Healthy male
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To investigate the effects of functional wear on recovery after high-load exercise
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Test wear
Interventions/Control_2 - Control wear
Eligibility:
Age-lower limit - 18
years-old
<=
Age-upper limit - Not applicable
Gender - Male
Key inclusion criteria - 1) Healthy Japanese males aged 18 years or older.
2) Individuals who regularly engage in high-intensity training and are judged to be capable of tolerating the exercise workload of this study based on the results of pre-test maximal oxygen uptake (VO2max) measurement or other evaluations.
3) Individuals who have provided voluntary written informed consent to participate in this study.
4) Individuals judged by the prinipal investigator or sub-investigator to have no problems participating in this study based on the results of screenings or tests.
Key exclusion criteria - 1) Individuals taking medications that affect hemodynamics for the treatment of cardiovascular disease, hypertension, or other conditions.
2) Individuals undergoing medical treatment or taking medication for sleep-related disorders, such as insomnia.
3) Individuals who routinely wear blood-circulation-enhancing garments.
4) Individuals with an underweight or obese body type.
5) Individuals with a smoking habit.
6) Individuals with a daily caffeine intake of 300 mg or more.
7) Individuals with an irregular lifestyle.
8) Individuals who have engaged in night-shift work (after 22:00) within the past 3 months.
9) Individuals who have traveled to a country with a time difference of 3 hours or more within the past 3 months.
10) Individuals who experience events during the study period that could pose a significant confounding effect on the measured outcomes.
11) Individuals otherwise judged to be inappropriate for participation in the study by the principal investigator or sub-investigator.
Target Size - 30
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2026 Year 06 Month 11 Day
Date of IRB - 2026 Year 06 Month 11 Day
Anticipated trial start date - 2026 Year 06 Month 17 Day
Last follow-up date - 2026 Year 09 Month 30 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070839
Disclaimer: Curated by HT Syndication.
