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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05857956
Other study ID # 20290
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 24, 2023
Est. completion date April 11, 2023

Study information

Verified date May 2023
Source Proper Wild, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date April 11, 2023
Est. primary completion date April 7, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - Currently experiencing symptoms associated with ADHD, including: Impulsiveness. Disorganization and problems prioritizing Poor time management skills Problems focusing on a task Trouble multitasking Excessive activity or restlessness Poor planning - Age 18-55 - Self-reported issues with focus and/or productivity - Generally healthy - don't live with any uncontrolled chronic disease Exclusion Criteria: - Currently taking prescription medication for ADHD - Currently supplementing with L-Theanine. - Known to respond negatively to caffeine (no effect, makes them sleepy or feel unwell) - People with a high caffeine tolerance defined as regular consumption of >400mg of caffeine (>4 coffees) per day. - Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders. - Anyone with known severe allergic reactions. - Women who are pregnant, breastfeeding, or attempting to become pregnant - Unwilling to follow the study protocol.

Study Design


Related Conditions & MeSH terms


Intervention

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.

Locations

Country Name City State
United States Citruslabs Santa Monica California

Sponsors (2)

Lead Sponsor Collaborator
Proper Wild, Inc. Citruslabs

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Attention-deficit/hyperactivity disorder (ADHD)-like symptoms. [Time Frame: Baseline to Day 28] Survey-based assessment (0-5) scale of changes in symptoms associated with ADHD. Parameters explored include focus & concentration, productivity, mood, and "brain fog". 28 days
Secondary Assess the product as a replacement for coffee or caffeinated beverages. [Time Frame: Baseline to Day 28] Survey-based assessment regarding changes in daily coffee/beverage consumption, stress, anxiety, jitters, energy crash, and gastrointestinal upset. Responses will be statistically analyzed and reported as % of subject responses. 28 days
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