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

Proper Wild, Inc.

Status: Completed

Conditions: Caffeine; Attention Difficulties; Mood; Anxiety; ADHD

Treatments: Other: Proper Wild energy shot

Study type: Interventional

Funder types: Industry

Identifiers

NCT05857956

20290

Details and patient eligibility

About

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.

Enrollment: 40 patients

Sex: All

Ages: 18 to 55 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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40 participants in 1 patient group

Proper Wild energy shot

Experimental group

Description:

Participants will take one bottle daily of Proper Wild Energy shot in the morning. Participants will be advised to drink one bottle in the morning, with or without a meal, depending on their preference, as a replacement for their usual first caffeinated beverage of the day.

Treatment:

Other: Proper Wild energy shot