MedTrace Logo

Investigation of Dietary Supplement Liquid Shot Products on Mental Energy, Cognition (Acuity),and Mood

NCT06384586 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2024-04-25

No results posted yet for this study

Summary

This is a single center, randomized, double blind, placebo-controlled, crossover study to determine the acute effect of a developmental dietary supplement liquid shot product on cognitive task performance and perceived effect measures related to mood and mental energy. The study will be conducted in healthy participants.

Conditions

  • Cognition
  • Mental Fatigue
  • Mood

Interventions

DIETARY_SUPPLEMENT

Placebo shot

60ml shot served in an amber bottle and consumed after 40 minutes of baseline assessments

DIETARY_SUPPLEMENT

Functional energy shot

60ml shot served in an amber bottle and consumed after 40 minutes of baseline assessments

Sponsors & Collaborators

  • HCD Research

    collaborator INDUSTRY

  • British American Tobacco (Investments) Limited

    collaborator INDUSTRY

  • The Water Street Collective

    lead INDUSTRY

Principal Investigators

  • Michelle M Niedziela, PhD · HCD Research

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-11-17
Primary Completion
2022-12-22
Completion
2022-12-22

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06384586 on ClinicalTrials.gov