Study Details

 

 

Looking for participants for a 7-week treatment study investigating effectiveness of a nutritional supplement on ADHD verses placebo. 

 

Participants will receive $200 at the conclusion of the study.

 

Interested participants will be screened.

 

A total of 6 office visits will be required to complete study, which includes screening visit, baseline visit, four follow-up visits and a final short telephone consult. Participants will be allowed to cross-over into a different treatment group after week 2. 

 

There are no charges for the office visits or nutritional product supplied; participants will be compensated $200 at last office visit.  

 

 

Study participants must:

• Be between 18-55 years old. 

• Been diagnosed with ADHD and/or meets the DSM-IV-TR diagnostic criteria for ADHD. 

• Have washout period from ADHD medication of at least 7-day (for stimulant treatments) or 28-day (for nonstimulant treatments) prior to the second office visit. 

• Participants can not be pregnant. 

• Overall good health, including healthy kidney function.

 

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You are ineligible for the study if you:

• Are a shift worker

• Suffer from a psychiatric disorder

• Have a neurological disorder

• Taking antidepressant, antipsychotic or an anticonvulsant medication

• If you suffer from a disorder where stimulants are contraindicated, e.g.  hypertension, cardiac disease, Tourette syndrome.

• If you have HIV or active Hepatitis C.

• Subject with history of significant gastrointestinal disease.