Overview
In this 8-week observational trial, we rigorously assessed the impact of Intellectra on cognitive performance in a diverse cohort of 213 adults.
The study demonstrated significant improvements in focus, alertness, and mental clarity. The following sections detail the experimental methodology and present the key results.

Methodology and structure
We recruited healthy adults with no known cognitive impairments.
A balanced mix of genders, age ranges, and occupational backgrounds ensured a wide variety of lifestyles and daily routines.
Week 0: Participants completed an initial survey to gauge their self-reported levels of focus, energy, mental clarity, and stress.
Cognitive Check: Basic memory and attention tasks established a starting point for each individual.
Participants were instructed to take two capsules of Intellectra once daily, ideally during their morning routine.
They were asked to maintain normal eating habits, physical activities, and sleep schedules for the duration of the study.
Weeks 1–7: Short online surveys measured subjective changes in focus, alertness, mood, and energy.
Digital Diaries: Participants were encouraged to note any noticeable effects, positive or negative, on concentration, productivity, or daily well-being.
Week 8: A concluding set of surveys and cognitive tasks measured any shifts from the baseline.
Exit Interviews: Select participants also participated in brief interviews to offer qualitative feedback.