Efficacy Assessment of Probiotics in Improving Sleep Indices

Status Recruiting

Clinical Trial Summary

To determine whether PS150 (1) reduces insomnia symptoms, (2) improves sleep quality, (3) adjusts autonomic nervous system functioning, (4) reduces the severity of anxiety and depressive symptoms, and (5) adjusts microbiome and endocrine functions.

Clinical Trial Description

One-hundred-forty participants with self-reported insomnia (PSQI≥ 7 & 22 > ISI ≥ 12) aged between 20 and 60 years old are estimated to be recruited and randomly assigned to two arms, the PS150 group and the placebo group, under the double-blinded trial. Participants take one capsule of probiotics or placebo after dinner for 30 days. Study measures include polysomnography (PSG), subjective sleep, depressive, and anxiety questionnaires, sleep diary, fecal sampling, saliva testing, and urine testing. ;

Study Design

Related Conditions & MeSH terms

Insomnia

Clinical Trial Details

NCT number	NCT06361368
Study type	Interventional
Source	National Yang Ming Chiao Tung University
Contact	Yu En Kuo, Master
Phone	+886 975231262
Email	iankuo1106@gmail.com
Status	Recruiting
Phase	N/A
Start date	April 11, 2024
Completion date	March 2026

View Details

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