Actively Recruiting
Patients At Risk for Sensory Screening (HPARSS) to Enhance Sensory Deficit Screening in Childhood Cancer Survivors
Led by Washington University School of Medicine · Updated on 2025-12-22
146
Participants Needed
1
Research Sites
147 weeks
Total Duration
On this page
Sponsors
W
Washington University School of Medicine
Lead Sponsor
S
St. Jude Children's Research Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Patients At Risk for Sensory Screening (HPARSS) to Enhance Sensory Deficit Screening in Childhood Cancer Survivors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients diagnosed with pediatric cancer before 18 years of age
- Received treatment including chemotherapy and/or radiation therapy
- Completed all cancer therapy at least 6 months ago but less than 2 years ago
- Followed in the Division of Pediatric Hematology/Oncology Program at Washington University School of Medicine
- Current age between 7 and 17 years
- English speaking
You will not qualify if you...
- Undergoing active cancer treatment
- Under the care of the Late Effects Program at St. Louis Children's Hospital
- Received previous diagnostic testing or rehabilitative therapy for a secondary deficit eligible for screening
- Parents and/or patient illiteracy
- No contact with treatment team in the past two years
- In foster care or without a legal guardian
AI-Screening
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Trial Site Locations
Total: 1 location
1
St. Louis Children's Hospital - Washington University School of Medicine
St Louis, Missouri, United States, 63110
Actively Recruiting
Research Team
R
Robert J Hayashi, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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