31 Day

Keto Brainz Nootropic Creamer Trial

STUDY TITLE Keto Brainz Nootropic Creamer Trial
Submitted under umbrella

Umbrella Protocol for Efforia Personalized Agentic Hypothesis Discovery & Experiential Proof Trials

Date submitted

Sep 8, 2026

End date

There is no pre-specified end date and sub-studies remain open long-term.

Language

English

Efforia AI IRB approval recommendation

—

Recruitment page preview

Preview

Informed consent

Review

Study author

Mollee Rucker

Principal investigator

Matthew Amsden

Sub-Investigator for Adverse Events

Dr. Viral Patel

Description

Participants will use Keto Brainz Nootropic Creamer 30-Serving once daily for 30 treatment days as part of a consistent beverage routine. The routine focuses on preparing and consuming one serving in the same general way each day, with attention to taste, convenience, and ease of use. The trial is designed around everyday fit, routine adherence, and subjective daily experience without adding extra wellness behaviors.

Participant engagement length

31 Days

Sponsor

This study is made possible by your payment to cover all supplies and expenses required to participate.

Cost to participant

$0

Included products & services

—

Outcome measures

Your Goals & Objective Expectations in this Study

Methodology

Single Arm longitudinal where participants act as their own control

Basic or advanced dissemination plan

Basic

Deviation from recruitment approach

No

Deviation from statistical approach

No

Will study include “more about you questions”

No

ClinicalTrials.gov

Yes

Commitment to list findings on ClinicalTrials.gov

Yes

This document is prepared with the assistance of AI, but is reviewed by a human.

Rational & Study Design

Reason I Created This Protocol:

Coffee add-ins get big promises online: sharper mornings, smoother routines, “main-character” energy. Research on habit formation, caffeine rituals, and self-tracking suggests consistency matters, but real-world fit is the missing piece. I created this study to see how a once-daily Keto Brainz Nootropic Creamer routine performs where it counts: your cup, your schedule, your standards, from Baseline to Day 34.

My Objective For You:

My objective is to help you evaluate whether one daily serving of Keto Brainz Nootropic Creamer fits your life without asking you to overhaul it. You’ll track your goals, expectations, adherence, taste, convenience, and subjective experience so you can see what the routine actually does for you from Baseline to Day 34.

Aims & Objectives:

This study aims to assess how a consistent daily creamer routine influences participant-reported expectations, routine adherence, ease of use, and everyday satisfaction over 30 treatment days through Day 34. You will receive personalized results so you can judge whether this product earns a regular spot in your mug, your morning, and your budget.

Significance & Impact:

This trial matters because wellness products often win attention before they earn trust; this protocol brings structure, consistency, and participant-level data to an everyday beverage habit. Expected outcomes include clearer insight into taste, convenience, adherence, and perceived daily fit, while limitations include subjective reporting, no disease-related claims, and no isolation of effects beyond the creamer routine itself.

The Intervention

Keto/nootropic creamers are popular on social media for claims of focus, energy, and “clean” coffee routines, but clinical evidence for meaningful cognitive benefit is limited and ingredient-dependent. Medical consensus does not support disease or performance claims without stronger trials. Many consumers perceive convenience and satiety benefits; risks may include caffeine sensitivity, GI upset, allergens, added fats/calories, cost, and overexpectation.

Included Products & Services

Study Design & Methodology

Inappropriate Participants & Inclusion/Exclusion

Study Design & Experience

Statistical Analysis Plan

Limitations & Justification

Human Subjects Ethics

Suitability Under Minimal Risk Umbrella Protocol

Suitability for Pay to Participate Model

Human Subjects Protection Questionnaire