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An Interactive Program to Improve Care for Children With CF
Not Recruiting
Trial ID: NCT00185549
Purpose
The purpose of this study is to evaluate the impact of an internet based program for children
and families (CF.DOC) with Cystic Fibrosis on health outcomes. The program provides for
virtual visits, a personal health record, messaging with clinicians and several tools for
monitoring self-care behaviors. We anticipate that this intervention will provide for more
intensive monitoring and feedback of self-care behaviors and will lead to improved health
status and in particular nutritional status
Official Title
An Interactive Program to Improve Care for Children With Cystic Fibrosis
Stanford Investigator(s)
Eligibility
Inclusion Criteria: Patients with Cystic Fibrosis diagnosed by a sweat chloride analysis
and/or testing for the CF gene between the ages of 1 month and 21 years of age. Patients
must also be English speaking -
Exclusion Criteria: Non-English speaking patients
-
Intervention(s):
behavioral: CF. DOC
Not Recruiting
Contact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305