Patient-Provider Tools to Improve the Transition to Adult Care in Sickle Cell Disease

Completed · Not applicable

Conditions studied: Sickle Cell Disease

In brief

The purpose of the study is to develop patient-provider clinical support tools to improve clinical practice, patient self-management, and disease outcomes in sickle cell disease during transition to adult care. The investigators hypothesize that these clinical support tools (patient tool, provider tool, and patient/parent web-based portal) will be feasible, user friendly, and beneficial. The investigators hypothesize that participants will demonstrate better disease self-efficacy at the end of the 6 week intervention and maintain these gains during the follow-up period (up to 1 year post-intervention).

Key facts

Study ID
NCT02200510
Run by
Children's Hospital Medical Center, Cincinnati
People needed
78
Starts
2011-06-01
Expected to finish
2015-08-01
Last updated by the study team
2018-06-15

Who can join

Age: 13 and older, up to 24. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.