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| Name | Class |
|---|---|
| St. Jude Children's Research Hospital | OTHER |
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients: Highlighting Patients at Risk for Sensory Screening (HPARSS) | Experimental |
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| Providers: Highlighting Patients at Risk for Sensory Screening (HPARSS) | No Intervention | -Providers will complete a survey regarding their views of the HPARSS. The Acceptability of Intervention Measure has 4 questions and the Feasibility of Intervention Measure has 4 questions. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Highlighting Patients at Risk for Sensory Screening (HPARSS) | Other | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of patients with at risk for sensory deficits identified by HPARSS | Through completion of enrollment for all patients (estimated to be 9 months) | |
| Percentage of at risk patients who fail the assigned screening test | Through completion of enrollment for all patients (estimated to be 9 months) | |
| Percentage of patients in need of referral for screen test results who participate in formal diagnostic testing and/or treatment | Through 1 year after the completion of screening test for all participants (estimated to be 1 year and 9 months) |
| Measure | Description | Time Frame |
|---|---|---|
| Number and types of barriers to participation in formal diagnostic testing and therapy in CCS failing to engage in sensory screening | At approximately 2 months following the patient's screening | |
| Number and types of facilitators to participation in formal diagnostic testing and therapy in CCS failing to engage in sensory screening |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Robert J Hayashi, M.D. | Contact | 314-454-6018 | hayashi_r@wustl.edu |
| Name | Affiliation | Role |
|---|---|---|
| Robert J Hayashi, M.D. | Washington University School of Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| St. Louis Children's Hospital - Washington University School of Medicine | Recruiting | St Louis | Missouri | 63110 | United States |
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| Label | URL |
|---|---|
| Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine | View source |
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|
| At approximately 2 months following the patient's screening |
| Acceptability of HPARSS as measured by the Acceptability of Intervention Measure (AIM) | -4 questions inquiring about the acceptability of HPARSS with answers ranging from completely disagree=1 to completely agree=5. The higher the score indicates higher acceptability of the HPARSS. | To be completed at the time of enrollment completion (approximately 9 months) |
| Feasibility of intervention as measured by Feasibility of Intervention Measure (FIM) | -4 questions inquiring about the feasibility of HPARSS with answers ranging from completely disagree=1 to completely agree=5. The higher the score indicates higher feasibility of the HPARSS. | To be completed at the time of enrollment completion (approximately 9 months) |
| ID | Term |
|---|---|
| D009369 | Neoplasms |
| D034381 | Hearing Loss |
| D010523 | Peripheral Nervous System Diseases |
| ID | Term |
|---|---|
| D006311 | Hearing Disorders |
| D004427 | Ear Diseases |
| D010038 | Otorhinolaryngologic Diseases |
| D012678 | Sensation Disorders |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009468 | Neuromuscular Diseases |
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