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Preliminary study about the association of the quality improvement of the sleep and health status

Preliminary study about the association of the quality improvement of the sleep and health status - Preliminary study about the association of the quality improvement of the sleep and health status

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000043805
Enrollment
100
Registered
2021-04-01
Start date
2021-01-26
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

Intake of test food daily intake, for 12 weeks. Participate in a sleep improvement program for 12 weeks.

Sponsors

EP Mediate Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Subjects who agree in writing to study participation and can inspect on predetermined inspection day (2) Subjects who are smartphone user, and use the bedclothing to get sleep data

Exclusion criteria

Exclusion criteria: (1) Subjects who were under treatment or have a history of serious diseases(e.g., diabetes, liver disease, kidney disease, or heart disease) (2) Subjects who have a disease that requires constant medication, subjects with serious diseases that require medication, and subjects who have history (3) Subjects who have history of mental illness (depression, etc.), chronic fatigue syndrome, insomnia, hypersomnia, circadian rhythm sleep disorder, parasomnia, etc (4) Subjects who are under treatment of sleep apnea syndrome (5) Subjects who are judged as unsuitable for the use environment based on the results of sleep improvement program (6) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (7) Subjects who have experienced abnormal clinical test values or cardiopulmonary function and have been judged to have problems participating in the study (8) Subjects at risk of developing allergy in relation to the study (9) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (10) Subjects who have participated in other clinical study within the last one month prior to the current study (11) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating (12) Subjects who are judged as unsuitable for the study by the investigator for other reason

Design outcomes

Primary

MeasureTime frame
Quality of the sleep by the sleep improvement program (awake time, deep sleep %)

Countries

Japan

Contacts

Public ContactSaki Fukuchi

EP Mediate Co., Ltd. Development Business Headquarters, TTC Center, Trial Planning Department

fukuchi473@eps.co.jp03-5657-4983

Outcome results

None listed

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