Clinical Trials Directory

Trials / Completed

CompletedNCT05857956

A Clinical Trial to Assess the Efficacy of a Plant-based Energy Shot on Focus and ADHD-like Symptoms

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Proper Wild, Inc. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

This is a virtual, single-arm clinical trial that will last 28 days. Participants will drink 1 bottle of Proper Wild energy shot daily and complete questionnaires at baseline, day 1, day 14, and day 28. Attention deficit hyperactivity disorder (ADHD)-like symptoms, such as concentration, focus, and attention, will be evaluated at baseline and at each check-in. Likert scale responses will be examined from baseline to each check-in. Participant responses on product feedback will be presented as % scores.

Conditions

Interventions

TypeNameDescription
OTHERProper Wild energy shot100% plant-based energy shot containing natural caffeine, L-Theanine, purified water, pineapple juice concentrate, natural flavors, kiwi juice concentrate, organic lemon juice concentrate, organic strawberry juice concentrate, monk fruit juice concentrate, pink himalayan sea salt.

Timeline

Start date
2023-02-24
Primary completion
2023-04-07
Completion
2023-04-11
First posted
2023-05-15
Last updated
2023-05-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05857956. Inclusion in this directory is not an endorsement.