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Sleep Status Verification Study Through Continuous Intake of Test Food

Sleep Status Verification Study Through Continuous Intake of Test Food: a randomized, double blind, placebo-controlled study - Sleep Status Verification Study Through Continuous Intake of Test Food

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060557
Enrollment
40
Registered
2026-02-03
Start date
2026-02-03
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 adult

Interventions

Continuous intake of one packet of the test article A daily before bedtime for 8 weeks. Continuous intake of one packet of the test article B daily before bedtime for 8 weeks. Continuous intake of one

Sponsors

Japan Clinical Trial Association
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects dissatisfied with or concerned about their sleep quality 2. Subjects experiencing fatigue in daily life 3. Subjects with a BMI between 19 and 26 4. Subjects who use a smartphone and can download and use an app.

Exclusion criteria

Exclusion criteria: 1. Subjects satisfied with their sleep quality, somewhat satisfied, or neither satisfied nor dissatisfied 2. Pregnant women, breastfeeding individuals, or those who may be pregnant 3. Subjects working night shifts or rotating day-night shifts 4. Subjects currently receiving medical treatment or taking prescription medication 5. Subjects diagnosed by a physician with sleep disorders such as insomnia 6. Subjects taking sleeping pills or sleep supplements (e.g., melatonin) 7. Subjects undergoing hormone replacement therapy 8. Subjects who participated in another human trial within the past month or are currently participating in one 9. Subjects whose trial date falls within 2 weeks of their most recent vaccination

Design outcomes

Primary

MeasureTime frame
OSA sleep inventory MA version, VAS, Instrumental measurement

Countries

Japan

Contacts

Public ContactTakeshi Kaneko

Japan Clinical Trial Association N.A.

info@yakujihou.org0364574666

Outcome results

None listed

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