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Trial Title: Patients At Risk for Sensory Screening (HPARSS) to Enhance Sensory Deficit Screening in Childhood Cancer Survivors

NCT ID: NCT05582551

Condition: Childhood Cancer

Conditions: Keywords:
childhood cancer survivors
electronic medical record
sensory deficit screening
hearing loss
peripheral neuropathy
vestibular
vision

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: Non-Randomized

Intervention model: Parallel Assignment

Primary purpose: Health Services Research

Masking: None (Open Label)

Intervention:

Intervention type: Other
Intervention name: Highlighting Patients at Risk for Sensory Screening (HPARSS)
Description: 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 HPARSS document.
Arm group label: Patients: Highlighting Patients at Risk for Sensory Screening (HPARSS)

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.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Patients with a diagnosis of pediatric cancer (diagnosis at <18 years of age) - Treatment including chemotherapy and/or radiation therapy - Completion of all cancer therapy for at least 6 months and less than 2 years - Followed in the Division of Pediatric Hematology/Oncology Program at the Washington University School of Medicine - Current age between 7 and 17 years of age (age where all of the screening tests are both valid and have been successfully performed by our group) - English speaking Exclusion Criteria: - Undergoing active cancer treatment - Patient 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

Gender: All

Minimum age: 7 Years

Maximum age: 17 Years

Healthy volunteers: No

Locations:

Facility:
Name: St. Louis Children's Hospital - Washington University School of Medicine

Address:
City: Saint Louis
Zip: 63110
Country: United States

Status: Recruiting

Contact:
Last name: Robert J Hayashi, M.D.

Phone: 314-454-6018
Email: hayashi_r@wustl.edu

Investigator:
Last name: Robert J Hayashi, M.D.
Email: Principal Investigator

Investigator:
Last name: Ashley Housten, OTD, MSCI
Email: Sub-Investigator

Investigator:
Last name: Caroline Mohrmann, PNP, Ph.D.
Email: Sub-Investigator

Investigator:
Last name: Thomas Kannampallil, Ph.D.
Email: Sub-Investigator

Investigator:
Last name: Patrick Lyons, M.D., MSc
Email: Sub-Investigator

Investigator:
Last name: Susan Hayashi, MA
Email: Sub-Investigator

Investigator:
Last name: Belinda Sinks, AUD
Email: Sub-Investigator

Investigator:
Last name: Anna Perlmutter, OTR/L
Email: Sub-Investigator

Investigator:
Last name: Feng Gao, M.D., Ph.D., MPH, MS
Email: Sub-Investigator

Start date: August 2, 2023

Completion date: May 31, 2025

Lead sponsor:
Agency: Washington University School of Medicine
Agency class: Other

Collaborator:
Agency: St. Jude Children's Research Hospital
Agency class: Other

Source: Washington University School of Medicine

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05582551
http://www.siteman.wustl.edu

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