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Study on the stress-relieving effects of Sea Buckthorn juice consumption.

Study on the stress-relieving effects of Sea Buckthorn juice consumption. - Study on the stress-relieving effects of Sea Buckthorn juice consumption.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055157
Enrollment
60
Registered
2024-12-31
Start date
2024-08-05
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

Healthy Adults

Interventions

Sponsors

Kansai University of Welfare Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) People who are temporarily fatigued or have reduced vitality due to desk-based work. (2) Men and women who can be judged to be healthy by the investigator based on medical examination data within the past three months. (3) Those with a BMI of less than 30 kg/m2 (4) Persons who can give written voluntary consent to participate in the trial. (5) Those who are able to drink Seabuckthorn Juice on a continuous basis.

Exclusion criteria

Exclusion criteria: (1) Persons currently receiving drugs for any disease (2) Persons who are consuming food or health food containing the ingredients of this test food. (3) Persons with serious diseases or psychiatric disorders of the glucose metabolism, lipid metabolism, liver function, renal function, heart, circulatory system, respiratory system, endocrine system, immune system, nervous system (4) Persons with a history of such diseases. (4) Persons with a history of abnormal laboratory values, which may be considered problematic for participation in the study (5) Persons with a disease undergoing treatment or with a history of a serious disease requiring medication (6) Persons at risk of developing allergies related to the study (7) Persons who are judged to be unsuitable as subjects based on the results of the lifestyle questionnaire (8) Those who are participating in other clinical studies at the start of the study (9) Those who are pregnant or plan to become pregnant or breastfeed during the study period (10) Persons who are deemed unsuitable to participate in the study by the study investigator (or the study manager).

Design outcomes

Primary

MeasureTime frame
Changes in stress states using the VAS method.

Secondary

MeasureTime frame
POMS2, Brief job Stress Questionnaire (BJSQ)

Countries

Japan

Contacts

Public ContactRyuji Takeda

Kansai University of Welfare Sciences Department of Nutritional Sciences for Welll-being Faculty of Health Science for Welfare

rtakeda@tamateyama.ac.jp072-978-0088

Outcome results

None listed

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