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Cancer Care Companion

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The Washington University

Status

Enrolling

Conditions

Pediatric Cancer

Treatments

Other: Cancer Care Companion

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07278778
1R21CA290223-01A1 (U.S. NIH Grant/Contract)
202601022

Details and patient eligibility

About

This study invites parents of children with cancer to use an electronic health record (EHR)-based communication tool, called the Cancer Care Companion, and assess the acceptability, appropriateness, and feasibility of the tool.

Full description

High-quality communication between clinicians and parents is critical to providing optimal care for pediatric cancer. This study engages parents of children with cancer to use an electronic health record (EHR)-based communication tool, called the Cancer Care Companion, and assess the acceptability, appropriateness, and feasibility of the tool. Parent participants will be given 3 months of access to Cancer Care Companion, after which the participant(s) will complete a semi-structured interview. Participants will also complete a survey of validated measures before and after the intervention.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Eligibility Criteria for Parents:

Parents of children with cancer will be enrolled if they meet the following criteria:

  • They are a legal guardian of a child diagnosed with cancer in the prior 4 weeks.
  • The child plans to receive or currently receives cancer directed therapy at St. Louis Children's Hospital.
  • The parent or legal guardian has access to internet through a computer or smart phone.
  • Speaks and reads in English
  • The parent or legal guardian agrees to enroll in Epic MyChart to access a proxy portal for their child.

Eligibility Criteria for Clinicians:

  • Clinicians with patients who have parents participating may be enrolled. Clinician participants will be employed at SLCH or Washington University School of Medicine (WUSM). The clinicians will include physicians, nurse practitioners, and nurse coordinators from the leukemia/lymphoma, brain tumor, and solid tumor teams in order to represent the breadth of pediatric cancer diagnoses.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

All Participants
Experimental group
Description:
All participants receive the Cancer Care Companion program. There is no control or comparison group.
Treatment:
Other: Cancer Care Companion

Trial contacts and locations

1

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Central trial contact

Bryan A Sisk, MD, MSCI

Data sourced from clinicaltrials.gov

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