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Effects of exercise and tea catechin intake on physical and mental function in middle-aged adults

Effects of exercise and tea catechin intake on physical and mental function in middle-aged adults - Effectiveness of exercise and tea catechin intake in middle-aged adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061326
Enrollment
100
Registered
2026-05-08
Start date
2026-05-10
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Middle-aged adults

Interventions

Intervention group: 24-week intervention period Tea catechin powder intake Resistance training (recommended: at least twice per week) Control group: 24-week intervention period Consumption of pla

Sponsors

Kagoshima University
Lead Sponsor
Central Research Institute, ITO EN Ltd
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Individuals without regular exercise habits 2) Men and women aged 40 to 64 years

Exclusion criteria

Exclusion criteria: 1) Those who do not intend to exercise during the period. 2) Those who drink green tea frequently (more than 4 cups per day) 3) Currently taking medication or receiving outpatient treatment for a serious medical condition 4) Those currently under medical supervision for exercise or diet therapy 5) Individuals for whom exercise is contraindicated by a physician's judgment 6) People who have ever felt unwell after the consumption of green tea 7) Individuals with a current or past history of drug or alcohol addiction 8) Individuals who are currently receiving outpatient treatment for mental disorders (e.g. depression) or sleep disorders, or who have a history of mental illness 9) Individuals with extremely irregular lifestyles and rhythms, such as eating and sleeping patterns 10) Pacemaker users 11) Individuals who have participated in other clinical trials (research) within 3 months prior to the date of consent, or who plan to participate in other clinical trials (research) during the study period 12) Persons who are unable to comply with the recording of compliance with the various survey forms 13) People with allergies to green tea, barley grass or starch 14) Individuals who are otherwise deemed ineligible

Design outcomes

Primary

MeasureTime frame
Physical function (handgrip strength, knee extension strength, chair stand test), body composition, and quadriceps muscle cross-sectional area

Secondary

MeasureTime frame
Physical activity, sleep quality, sleep duration, and sleep efficiency

Countries

Japan

Contacts

Public ContactDaijo Shiratsuchi

Kagoshima University Department of Physical Therapy, School of Health Sciences, Faculty of Medicine

shiratsuchi@health.nop.kagoshima-u.ac.jp099-275-5111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026