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
Who can participate
Age range17 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion 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 CA, CT, MA, ME, NH, NJ, NY or RI
✓. Provider approval for permission to approach
✓. Child undergoing allogeneic HSCT for treatment of cancer
Exclusion criteria
✕. 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, DFCI 25-001). Co-enrollment on a poverty intervention study would confound the specified endpoints of these open trial correlative studies
✕. Planned transfer of child to a non-DFCI, non-Columbia, or non UCSF 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, DFCI 25-001). Co-enrollment on a poverty intervention study would confound the specified endpoints of these open trial correlative studies