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NCT06283251Recruiting

PediRISE Feasibility

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

Source: ClinicalTrials.gov · Last updated 5 Oct 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
22 Feb 2024
Start date
15 May 2024
Primary completion date
30 Jun 2027
Lead sponsor
Dana-Farber Cancer Institute
NCT number
NCT06283251

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 15 May 2024 to the primary completion date, 30 Jun 2027
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Cohort 1: Poverty-exposed children with cancer receiving front-line 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
  • Child or household member receiving SSI
    • Cohort 2: Poverty-exposed children with cancer undergoing HSCT
  • 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
  • Child previously received RISE intervention
  • Child or household member receiving SSI

Other illness

  • Planned transfer of child to a non-DFCI or non-Columbia facility for cancer-directed therapy
  • Planned transfer of child to a non-DFCI, non-Columbia, or non UCSF facility for cancer-directed therapy

Who the study is looking for

  • Cohort 1: Poverty-exposed children with cancer receiving front-line cancer-directed therapy
  • 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
    • Cohort 2: Poverty-exposed children with cancer undergoing HSCT
  • Child undergoing allogeneic HSCT for treatment of cancer
  • Child has established care at a study site and is between 30 days prior to start of planned conditioning through day +7 of HSCT at time of enrollment
  • Child planned to receive follow-up care after discharge for HSCT at study site
  • Child is \<18 years at the time of enrollment
  • Parent/guardian screen 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

Age in the registry: - to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Dana-Farber Cancer Institute
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting
Boston Children's Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting
Columbia University Medical Center
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
University of California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.