Dietary Supplement Participants in this arm will receive a daily dose of a dietary supplement for 60 consecutive days. The supplements are administered orally and aims to improve cognitive performance in university students. Participants will also complete cognitive assessments before starting supplementation, 30 days after, and at the end of the intervention.

Participants in this arm will receive a daily dose of an inert placebo that matches the supplement in appearance, taken orally for 60 consecutive days. The placebo is used as a control to compare the effects of the dietary supplement on cognitive performance. Participants will undergo the same cognitive assessments as the experimental groups.

Dietary Supplements Participants in this arm will receive a daily dose of two dietary supplement for 60 consecutive days. The supplements are administered orally and aims to improve cognitive performance in university students. Participants will also complete cognitive assessments before starting supplementation, 30 days after, and at the end of the intervention

Change in cognitive performance measured Self-efficacy scale in higher education before starting supplementation, 30 days after, and at the end of the intervention. For reference, scores in the different dimensions (academic, higher education regulation, and social interaction) equal to or less than 3 indicate low levels of self-efficacy in the respective dimension. In turn, scores equal to or greater than 5 correspond to robust self-efficacy beliefs.

Change in mood is measured by DASS before starting supplementation, 30 days after, and at the end of the intervention. In the DASS, the scores are presented as a total score (between 0 and 63) and a score for the three subscales (between 0 and 21). The scores for each subscale are categorized into five degrees of severity: normal, mild, moderate, severe, and extremely severe. The higher the score, the greater the degree of severity.

Psychological pathology assessment is measured by BSI before starting supplementation, 30 days after, and at the end of the intervention. BSI is assessed by calculating the Overall Severity Index (OSI), adding up all items on the BSI-18. OSI values ≥ 63 indicate psychological pathology.

The shorter version of the Nutrition Council Appetite Assessment Questionnaire-the Simplified Appetite Nutrition Questionnaire (SANQ)-is being used in this study as a tool for measuring appetite in the group of participants. The SANQ consists of four items, grouped into a single domain. When added together, they generate the total questionnaire score, which can range from 4 to 20. The lower the score, the greater the risk of weight loss. In the original instrument, scores lower than or equal to 14 indicate a risk of weight loss of at least 5% in six months. Participants will be assessed before taking the dietary supplement and 60 days after.