There are three basic steps to participation in the PROS Febrile Infant Study:
| Step 1. | Identify an On-site Research Coordinator |
| | Identify an on-site research coordinator(s) to manage day-to-day study activities and communicate with PROS Central. |
| Step 2. | Determine Eligibility of All Patients | |
| | Age: | | Under three months. |
| | Fever: | | A rectal, axillary or tympanic temperature greater than or equal to 38.0 degrees C or greater than or equal to 100.4 degrees F in the office. |
| | Practitioner: | | Initial clinical assessment and management done by a PROS member. |
| | Consent: | | No parental consent is needed for this study. |
| Step 3. | Enroll Consecutive Study-Eligible Patients |
| | Record all study-eligible patients in patient information log. |
| | Complete data collection forms as required: Medical Examination Form, Hospital Follow-Up Form, and Outpatient Follow-Up Form. |
| | Mail completed patient envelopes back to PROS Central. |
IMPORTANT NOTE: There is reimbursement for participation in this study! Practitioners will be paid $100 for the first patient enrolled and $10 for every patient enrolled thereafter. Reimbursements will be paid approximately every 3 months for complete enrollments as defined above.