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A study on the effect of the intake of fermented ginseng-containing food on stress

A study on the effect of the intake of fermented ginseng-containing food on stress - A study on the effect of the intake of fermented ginseng-containing food on stress

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022943
Enrollment
40
Registered
2016-08-05
Start date
2016-08-06
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 adult

Interventions

Ingestion of test food containing fermented ginseng for 8 consecutive weeks Ingestion of placebo without fermented ginseng for 8 consecutive weeks

Sponsors

TTC Co.,Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Male and female workers from 30 to 60 years old 2) POMS2-AS FI T score is 50 and more, and VA T score is 50 and less

Exclusion criteria

Exclusion criteria: 1)Subjects who routinely use food or medicine containing of ginsenosides 2)Subjects who perform an act for the improvement of the fatigue, the quality of the sleep and stress 3)Subjects who wake after sleep onset for nocturia twice and more than twice a week 4)Night and day shift worker or manual laborer 5)Subjects who have a disease on treatment or are judged to that medical treatment are necessary by the doctor 6)Subjects who are under treatment or a history of sleep apnea syndrome or are strongly suspected of having sleep apnea syndrome 7)Subjects diagnosed with chronic fatigue syndrome 8)Subjects who were under treatment or have a history of serious diseases (e.g., diabetes, liver disease, kidney disease, or heart disease) 9)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire and other questionnaires 10)Subjects having possibilities for emerging allergy related to the study 11)Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination 12)Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study 13)Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating 14)Subjects who are judged as unsuitable for the study by the investigator for other reason

Design outcomes

Primary

MeasureTime frame
Stress:POMS2-AS Sleep:AIS, PSQI-j

Countries

Japan

Contacts

Public ContactEtsushi Yamamoto

TTC Co.,Ltd. Clinical Research Planning Department

e.yamamoto@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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