Actively Recruiting
A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications
Led by Outliers, Inc. · Updated on 2026-02-02
90
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
O
Outliers, Inc.
Lead Sponsor
C
Citruslabs
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the effects of the Stasis dietary supplement on reducing oxidative stress, cortisol levels, and side effects related to stimulant medications used for ADHD in adults aged 18 to 55. This randomized, triple-blind, placebo-controlled clinical trial aims to understand how the supplement may help with symptoms like sleep difficulties, irritability, anxiety, and brain fog over a three-month period. The study is sponsored by Outliers, Inc. and includes participants who are stable on stimulant medication and supplements. Participants are randomly assigned to either the Stasis supplement group or a placebo group. The Stasis supplement is taken twice daily: the daytime dose with stimulant medication and food, and the nighttime dose 30 minutes before bedtime on an empty stomach. The placebo is designed to match the supplement in taste and appearance. The trial lasts three months, during which both groups follow their usual stimulant medication and habits. During the study, researchers will measure changes in oxidative stress and cortisol levels at the beginning and end of the trial. They will also assess sleep quality, irritability, focus, sociability, mood, stress, appetite, and blood levels of Vitamin C and CoQ10 monthly. Safety and adherence will be monitored throughout. Participants are expected to maintain stable medication and supplement use and will be followed for the full three-month duration.
CONDITIONS
Brief Title
A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18-55 years
- Currently prescribed stimulant medication for ADHD
- Experiencing sleep difficulty, irritability, anxiety, or brain fog
- Stable medication dose for at least 3 months
- Generally healthy with no uncontrolled chronic conditions
- Stable on supplements for at least 3 months if applicable
- US resident
- Willing to maintain current habits during the study
You will not qualify if you...
- Chronic conditions such as cancer or mental illness
- Use of psychiatric medications other than stimulants
- Pregnancy or breastfeeding
- Thyroid, liver, or kidney conditions
- Recent smoking or heavy alcohol use
- Night shift work
- Participation in other clinical trials
- Allergies to ingredients in the study product
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 months
Participants take the supplement or placebo daily alongside their stimulant medication to evaluate effects on side effects associated with stimulant use.
Visits at baseline, Month 1, Month 2, and Month 3
Trial Site Locations
Total: 1 location
1
Citruslabs
Las Vegas, Nevada, United States, 89118
Actively Recruiting
Research Team
P
Patrick Renner, MSc
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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