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A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications

RECRUITINGN/ASponsored by Outliers, Inc.
Actively Recruiting
PhaseN/A
SponsorOutliers, Inc.
Started2025-08-12
Est. completion2026-03
Eligibility
Age18 Years – 55 Years
Healthy vol.Accepted
Locations1 site

Summary

This is a hybrid, two-arm, triple-blind, placebo-controlled, randomized clinical trial evaluating the efficacy of the Stasis supplement on reducing oxidative stress, cortisol levels, and side effects associated with stimulant medications used for ADHD over a three-month period in adults.

Eligibility

Age: 18 Years – 55 YearsHealthy volunteers accepted
Inclusion Criteria:

* Aged 18-55 years
* Currently prescribed stimulant medication for ADHD
* Experiencing: sleep difficulty, irritability, anxiety, brain fog
* Stable medication dose ≥3 months
* Healthy with no uncontrolled chronic conditions
* Stable on supplements ≥3 months if applicable
* US resident
* Willing to maintain current habits

Exclusion Criteria:

* Chronic conditions (e.g. cancer, mental illness)
* Use of psychiatric medications besides stimulants
* Pregnancy, breastfeeding, thyroid, liver, kidney conditions
* Recent smokers or heavy alcohol use
* Night shift workers
* Participation in other clinical trials
* Allergies to product ingredients

Conditions4

ADHDAnxietyBrain FogSleep Disturbance

Locations1 site

Citruslabs
Las Vegas, Nevada, 89118
Patrick Renner, MSc424-245-0284hello@citruslabs.com

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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