RecruitingNot ApplicableNCT07380412
A Study to Evaluate the Effects of a Supplement on the Side Effects Associated With Stimulant Medications
Sponsor
Outliers, Inc.
Enrollment
90 participants
Start Date
Aug 12, 2025
Study Type
INTERVENTIONAL
Conditions
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
Min Age: 18 YearsMax Age: 55 Years
Inclusion Criteria8
- 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 Criteria7
- 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
Interventions
DIETARY_SUPPLEMENTStasis Daytime and Nighttime
Daytime taken with stimulant medication and food. Nighttime taken 30 minutes before bedtime on an empty stomach.
DIETARY_SUPPLEMENTPlacebo
Matched placebo product in taste and appearance.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07380412
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