RECRUITING

PediRISE Feasibility

Description

The goal of this research study is to learn whether investigators can successfully give the PediRISE program to families-in other words, whether most families are interested in participating in a study about the PediRISE program, including a 50-50 chance of receiving standard usual care, and a 50-50 chance of receiving the PediRISE support program. The names of the study groups in this research study are: * PediRISE Program Group * Usual Care Group

Conditions

Pediatric CancerFinancial StressFinancial HardshipDisparities
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Related Conditions:

Pediatric CancerFinancial StressFinancial HardshipDisparities

Study Overview

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Study Details

Study overview

The goal of this research study is to learn whether investigators can successfully give the PediRISE program to families-in other words, whether most families are interested in participating in a study about the PediRISE program, including a 50-50 chance of receiving standard usual care, and a 50-50 chance of receiving the PediRISE support program. The names of the study groups in this research study are: * PediRISE Program Group * Usual Care Group

Pilot Randomized Pediatric RISE (Resource Intervention to Support Equity) Feasibility Study

PediRISE Feasibility

Condition
Pediatric Cancer
Intervention / Treatment

-

Contacts and Locations

Boston

Boston Children's Hospital, Boston, Massachusetts, United States, 02215

Boston

Dana Farber Cancer Institute, Boston, Massachusetts, United States, 02215

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Child diagnosed with de novo cancer
  • * Child has established care at a study site and initiated cancer-directed therapy in the prior 2-months
  • * Child planned to receive at least 4-months of cancer-directed therapy at study site from time of diagnosis per initial cancer treatment plan
  • * Child is \<18 years at time of enrollment
  • * Parent/guardian screened positive for self-reported low-income (\<200% FPL).
  • * Family primary residence in MA, NY or NJ
  • * Provider approval for permission to approach
  • * Planned transfer of child to a non-DFCI or non-Columbia facility for cancer-directed therapy
  • * Foreign national family receiving care as an Embassy-pay patient
  • * Child is enrolled on embedded correlative health equity aims of open or upcoming clinical drug trials which are powered on descriptive parent-reported poverty data (e.g. AALL1731, AHOD2131, ANBL2131, DFCI 23-001).
  • * Child or household member receiving SSI.

Ages Eligible for Study

to 17 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Dana-Farber Cancer Institute,

Kira Bona, MD, MPH, PRINCIPAL_INVESTIGATOR, Dana-Farber Cancer Institute

Study Record Dates

2024-12-31