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Investigation of a Dietary Supplement Liquid Shot Product on Aspects of Mood Both At Rest and During a Laboratory Stressor Task.

NCT06785142 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2025-01-21

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 of aspect of mood both at rest and during laboratory stressor task. The study will be conducted in healthy adult participants.

Conditions

  • Mood
  • Stress
  • Alertness

Interventions

DIETARY_SUPPLEMENT

Functional Shot

60ml functional energy shot contained a proprietary blend of L-theanine, chamomile, lemon balm, ginseng and vitamins

DIETARY_SUPPLEMENT

Placebo Shot

Placebo 60 ml Shot, matched in volume, taste and colour and but did not contain any active ingredients

Sponsors & Collaborators

  • HCD Research

    collaborator INDUSTRY

  • British American Tobacco (Investments) Limited

    collaborator INDUSTRY

  • The Water Street Collective

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
29 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-01-14
Primary Completion
2023-03-22
Completion
2023-03-22

Countries

  • United Kingdom

Study Locations

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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 NCT06785142 on ClinicalTrials.gov