Randomized controlled trial to reduce stress

Randomized controlled trial to reduce stress - Randomized controlled trial to reduce stress

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000023903

Enrollment

Registered

2016-09-05

Start date

2014-09-24

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

None listed

Interventions

Self-help stress care program and functional peptide drink for 6 weeks everyday Self-help stress care program for 6 weeks everyday Placebo program for 6 weeks everyday

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Healthy males and females aged 20 years or more. 2) Subjects who can make self-judgment and agree to participate this trial.

Exclusion criteria

Exclusion criteria: 1)Subjects who take continuous medical treatment. 2)Subjects who are pregnant or have possibility to become pregnant or planning to become pregnant during the study or breast-feeding woman. 3)Subjects who have allergic reaction to food. 4)Subjects who are judged as unsuitable for the study by the principal investigator for other reasons.

Design outcomes

Primary

Measure	Time frame
Stress reaction, administered before and after the trial (6W); the Tension-Anxiety (TA), Depression (D), and Fatigue (F) subscales of the POMS	—

Secondary

Measure	Time frame
Somatosensory Amplification Scale , Medical Symptom Checklist, General Self Efficacy Scale	—

Countries

Japan

Contacts

Public ContactYuji Nonaka

Suntory Global Innovation Center Ltd. Innovation Development Department

Yuji_Nonaka@suntory.co.jp050-3182-0587

Outcome results