The effect verification of singing on karaoke in the stressful society and preliminary study for elder contents development -A study of the improving effects of singing on karaoke in stress, immunity and oral functions targeting those who suffer from stress -

The effect verification of singing on karaoke in the stressful society and preliminary study for elder contents development -A study of the improving effects of singing on karaoke in stress, immunity and oral functions targeting those who suffer from stress - - The effect verification of singing on karaoke in the stressful society and preliminary study for elder contents development

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000028992

Enrollment

Registered

2017-09-04

Start date

2013-03-15

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

Male and female aged 20 years over

Interventions

Singing on karaoke on karaoke using DAM (Daiichikosyo Amusement Multimedia) four times a week (for one hour a day) for 8 weeks

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1)Male and female who aged 20 or older at the time of consent acquisition (2)Subjects who can sing on karaoke singing about four times a week (1 hour per time) (3)Subjects who show understanding of the study procedures and agreement with participating the study by written informed consent prior to the study

Exclusion criteria

Exclusion criteria: (1)Subjects who have previous and/or current medical history of serious heart, lung, kidney, digestive organ (including gastrectomy), blood, endocrine, or metabolic disease or current treatment for these diseases (2)Subjects who regularly use health foods for modulating stress or immunity (3)Subjects who are administered medicines related to respiratory, cardiac and vascular diseases (4)Subjects who are difficult to visit the hospital (5)Subjects who are depressed and unstable in mental condition or have ahigh psychogenic response (6)Subjects who have been determined ineligible by principal investigator or sub-investigator

Design outcomes

Primary

Measure	Time frame
* VAS questionnaire	—

Secondary

Measure	Time frame
Saliva test Swallowing function test Blood test Urinaly test *POMS	—

Countries

Japan

Contacts

Public ContactKatsuhisa Sakano

CPCC Co., Ltd. Clinical Research Planning Department

cpcc-contact@cpcc.co.jp03-5297-3112

Outcome results

None listed

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