About this trial
This is a randomized, double-blind, placebo-controlled pilot study designed to evaluate the effect of an oral nutritional supplement containing Melissa officinalis formulated in phospholipids on mood and cortisol levels in healthy adults. Participants will be randomly assigned to receive either the active supplement or a placebo daily for 3 weeks. The primary outcome measures include changes in mood well-being, perceived stress, and salivary cortisol levels. The study aims to assess both efficacy and safety of the supplement in modulating stress response and emotional balance.
Eligibility criteria
Qualifiers
Age between 18 and 65 years
Healthy volunteers as assessed by medical history and physical examination
Willingness to comply with the study procedures
Disqualifiers
Current use of medications or supplements that may affect mood or cortisol levels
Known allergy or sensitivity to Melissa officinalis or phospholipids
History of psychiatric disorders (e.g., major depression, anxiety disorders)
Significant comorbidities (e.g., cardiovascular, hepatic, renal diseases)
Trial design
Treatments tested in this trial
- Melissa officinalis supplement