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Effects of Functional Recovery Wear on Recovery After High-Load Exercise

Effects of Functional Recovery Wear on Recovery After High-Load Exercise - Effects of Functional Recovery Wear on Recovery After High-Load Exercise

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061910
Enrollment
30
Registered
2026-06-16
Start date
2026-06-17
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy male

Interventions

Sponsors

EUPHORIA Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

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.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
Time-course changes and between-trial comparisons of salivary cortisol levels up to 120 minutes post-exercise.

Secondary

MeasureTime frame
Time-course changes and between-trial comparisons of heart rate variability indices during acute recovery up to 120 minutes post-exercise. Time-course changes and between-trial comparisons of subjective scores using the Visual Analog Scale up to 120 minutes post-exercise. Daily physical conditions and training workload from 7 days prior to the test to the end of the study.

Countries

Japan

Contacts

Public ContactYuki Urushizawa

EUPHORIA Co., Ltd. Corporate Business Division

yuki.urushizawa@eu-phoria.jp03-6388-9260

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026