L-theanine improves sleep quality and reduces stress markers in individuals with mild to moderate sleep disturbances
This study protocol describes a randomized, double-blind, placebo-controlled trial evaluating the effects of L-theanine (100mg, 200mg, 400mg) on sleep and stress markers in 60 healthy adults aged 18-65 with mild to moderate sleep disturbances. The primary outcomes are changes in objective and subjective sleep quality parameters and secondary outcomes include biochemical, physiological, and subjective stress markers after a 14-day intervention. The trial aims to determine the optimal dose of L-theanine for improving sleep and stress.
Evidence Score
Study Evidence
Study 1. The effect of green tea amino acid L-theanine formulation on markers of stress and quality of sleep (THESleep project) - a study protocol for a pilot randomised control trial.
observationalBulman A, McKune A, Georgousopoulou E, Sergi D, Naumovski N ยท Contemporary clinical trials (2026)
Result:
Mechanism Graph
Limitations
- โ This is a study protocol, not results; no data on actual effects are reported
- โ Small sample size (n=60) may limit generalizability
- โ Short intervention period (14 days) may not capture long-term effects
Frequently Asked Questions
What is L-theanine?โผ
L-theanine is a non-proteinogenic amino acid found primarily in tea leaves (Camellia sinensis) and is known for potential nootropic effects.
What doses of L-theanine are being tested?โผ
The study tests three doses: 100mg, 200mg, and 400mg per day in a functional beverage.
Who can participate in this study?โผ
Healthy adults aged 18-65 with mild to moderate sleep disturbances are eligible.
What outcomes are being measured?โผ
The study measures objective and subjective sleep quality, as well as biochemical, physiological, and subjective stress markers.
Products
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References
- 1.Bulman A, McKune A, Georgousopoulou E, Sergi D, Naumovski N. "The effect of green tea amino acid L-theanine formulation on markers of stress and quality of sleep (THESleep project) - a study protocol for a pilot randomised control trial.." Contemporary clinical trials, 2026. PMID: 41991056 DOI: 10.1016/j.cct.2026.108306