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
| Type | Name | Description |
|---|---|---|
| OTHER | Proper Wild energy shot | 100% 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.