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Clinical Trial Summary

The overall goal of this study is to attempt to overcome the organizational barriers that impede prompt screening for at-risk sensory deficits in childhood cancer survivors (CCS). Using a cross sectional design study, collaborators in the Informatics Research branch of the Institute of Informatics at the Washington University School of Medicine will identify CCS at risk for sensory deficits based upon their therapy exposure to generate the highlighting patients at risk for sensory screening (HPARSS) document. The investigators will utilize the HPARSS that will link therapy related risks for sensory deficits to specific screening procedures prompting the primary oncology provider to implement screening, diagnostic testing, and therapy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05582551
Study type Interventional
Source Washington University School of Medicine
Contact Robert J Hayashi, M.D.
Phone 314-454-6018
Email hayashi_r@wustl.edu
Status Recruiting
Phase N/A
Start date August 2, 2023
Completion date May 31, 2025

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