Actively Recruiting

Phase Not Applicable
Age: 0 - 17Years
All Genders
NCT06283251

PediRISE Feasibility

Led by Dana-Farber Cancer Institute · Updated on 2026-02-10

40

Participants Needed

4

Research Sites

163 weeks

Total Duration

On this page

Sponsors

D

Dana-Farber Cancer Institute

Lead Sponsor

A

American Cancer Society, Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

PediRISE Feasibility

Who Can Participate

Age: 0 - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Child diagnosed with new cancer
  • Child has started cancer treatment at a study site within the past 2 months
  • Child planned to receive at least 4 months of cancer treatment at the study site
  • Child is younger than 18 years at enrollment
  • Parent or guardian reports household income below 200% of the Federal Poverty Level
  • Family lives in CA, CT, MA, ME, NH, NJ, NY, or RI
  • Provider approval to approach the family
  • Child undergoing allogeneic HSCT for cancer treatment
  • Child is between 30 days before planned HSCT conditioning and day +7 of HSCT at enrollment
  • Child planned to receive follow-up care at the study site after HSCT discharge
Not Eligible

You will not qualify if you...

  • Planned transfer of child to a non-DFCI, non-Columbia, or non-UCSF facility for cancer treatment
  • Family is a foreign national receiving care as an Embassy-pay patient
  • Child enrolled in other clinical drug trials focused on poverty data that would conflict with this study
  • Child or household member receiving Supplemental Security Income (SSI)
  • Child previously received the RISE intervention

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

University of California San Francisco

San Francisco, California, United States, 94143

Actively Recruiting

2

Boston Children's Hospital

Boston, Massachusetts, United States, 02215

Actively Recruiting

3

Dana Farber Cancer Institute

Boston, Massachusetts, United States, 02215

Actively Recruiting

4

Columbia University Medical Center

New York, New York, United States, 10032

Actively Recruiting

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Research Team

K

Kira Bona, MD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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