Attention Deficit/Hyperactivity Disorder Internet Survey Study in a College Student Population

This is an investigator-blinded, prospective study of subjects diagnosed with
ADHD.Forty-four subjects ages 18 years and older will be enrolled. An Internet-based survey
will be piloted to evaluate its effect on adherence to oral ADHD medication. Subjects
randomized in a 1:1 ratio to the Internet-survey group will log their impression of the
state of their disease on a weekly basis. Subjects in both the intervention and control
groups will receive standard-of-care medication, stimulants. Adherence to the medication
will be assessed using Medication Event Monitoring System (MEMS®) caps, electronic monitors
affixed to the medication containers. Investigators and subjects will be blinded to the
adherence data until the final (Month 2) treatment visit.

Inclusion Criteria:

- Any male or female 18 years or older of age with a diagnosis of mild to severe ADHD
by a psychiatrist at Wake Forest University Student Health Clinic

- Use of the Wake Forest University Student Health Clinic Pharmacy to fill medication
for ADHD

- Subject is a good candidate to receive a stimulant for the treatment of their ADHD

- Subject is capable of understanding and willing to provide a signed and dated written
voluntary informed consent before any protocol specific procedures are performed

- The subject is able to complete the study and comply with study instructions,
including attending all study visits

- Will be filling a prescription for ADHD

Exclusion Criteria:

- Subject is less than 18 years of age

- Inability to complete all study-related visits or inability to complete the Internet
survey due to inadequate Internet access

- Patients who are homicidal, suicidal, or psychotic

- Female patients whose medications may be harmful during pregnancy must be on an
acceptable form of birth control, otherwise they will not be eligible for
participation