PediCARE Health Equity Intervention in High-Risk Neuroblastoma

Not Applicable

Withdrawn

• Conditions: Poverty; High-risk Neuroblastoma; Neuroblastoma; Disparities; Financial Stress; Pediatric Cancer
• Interventions: Behavioral: PediCARE Intervention

• Registration Number: NCT06335745
• Lead Sponsor: Dana-Farber Cancer Institute

Brief Summary

This is a randomized Phase II trial evaluating the addition of the Pediatric Cancer Resource Equity (PediCARE) health equity intervention to usual supportive care for poverty-exposed children with newly diagnosed high-risk neuroblastoma.

The names of the intervention groups in this research study are:

* Usual supportive care

* PediCARE + usual supportive care

Detailed Description

This is a randomized Phase II trial evaluating the addition of the Pediatric Cancer Resource Equity (PediCARE) health equity intervention to usual supportive care for poverty-exposed children with newly diagnosed high-risk neuroblastoma.

Participants will be randomized into one of two groups: Usual Supportive Care vs. PediCARE + Usual Supportive Care. Randomization means a participant is placed into a group by chance.

Participation in this research study is expected to last 6-months.

It is expected about 130 people will participate in this research study.

Study Timeline

• Study First Submitted: 2024-03-14
• Study First Submitted QC: 2024-03-21
• Study First Posted: 2024-03-28
• Status Verified: 2024-08
• Last Update Submitted: 2024-08-02
• Last Update Posted: 2024-08-05
• Study Start: 2024-09
• Primary Completion: 2028-09
• Study Completion: 2028-09

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Patient must have a new diagnosis of high-risk neuroblastoma.

• Patient must be enrolled on APEC14B1 and must have consented to future contact on APEC14B1.

• Patient must be enrolled on ANBL2131.

• Patient aged 0-17 years at the time of consent to ANBL2131.

• Patient must have opted-in to embedded optional ANBL2131 Household Survey.

• Family screened positive for HMH or low-income on ANBL2131 Household Survey. *

• Patient has not yet initiated Induction Cycle 3 on ANBL2131.

• Patient being treated at a U.S. site.

• Patients of all languages are eligible to participate.

  • Eligibility based on Household Survey will be determined by central study team review. HMH exposure will be operationalized as the report of at least one of the following four concrete resource insecurities: (1) Food insecurity, (2) Housing Insecurity, (3) Utility Insecurity, (4) Transportation Insecurity. Low-income will be defined as reported annual household income of less than 200% federal poverty level (FPL).

Exclusion Criteria

-Patient has transferred to ANBL1531 Arm E.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Arm 1: PediCARE + Usual Supportive Care Experimental	PediCARE Intervention	Participants will be randomized in a 1:1 ratio and stratified according to treatment group and household material hardship (HMH) severity group and participant parents/guardians will complete: * Remote baseline visit with introduction to PediCARE intervention by central study team * Parent completion of baseline survey. * Receipt of monthly PediCARE resource provisions x 6-months. * Parent completion of 3-month follow-up survey. * Parent completion of 6-month follow up survey and end of intervention period.

Primary Outcome Measures

Name	Time	Method
Change in Kessler-6 Psychological Distress Scale Score	At baseline and 3 months	As measured by the Kessler-6 Psychological Distress Scale (K6), a 6-item measure for the level of psychological distress in the past month. Responses are scored on a 5-point Likert scare with answers ranging from 0 "None of the time" to 4 "All of the time," and with a total score range of 0 - 4. Scores \> or = 7 suggest "high" distressed and those \> or = 13 meet criteria for serious or debilitating psychological distress. A t-test of differences in mean change scores of parent/guardian psychological distress from T1 (baseline) to T2 (3 months) will be used to compare across PediCARE and usual supportive care arms. The distribution of parent psychological distress scores across PediCARE and usual supportive care arms will also be descriptively characterized. The descriptive analyses will be intention-to-treat, defined as all randomized participants with at least one post-baseline contact or follow-up measure.

Secondary Outcome Measures

Name	Time	Method
Proportion of Enrolled Participants (Feasibility)	5 years	Feasibility of conducting a centrally-administered companion health equity intervention study among COG trial-enrolled participants will be described using proportions and 95% confidence intervals. Successful feasibility is defined as \>75% consent to participation and randomization and \<20% attrition. Feasibility metrics will be collected and monitored in real time throughout the duration of the study (about 5 years). An interim analysis for early stopping will also be conducted halfway through accrual (n=40 participants) to assess futility of the feasibility endpoint.
Change in Mean Household Material Hardship (HMH) Score	At baseline and 3-months	Household Material Hardship (HMH) information will via parent/guardian-completed survey instruments using standardized measures of housing, food, utility, and transportation insecurity. HMH scores will be calculated based on parent/guardian responses and will range from 0-4 based on the number of discrete areas of insecurity endorsed by participants. A t-test of differences in mean HMH change scores from T1 (baseline) to T2 (month 3) will be used to compare across PediCARE and usual supportive care arms. Investigators will also characterize the distribution between T1 and T2 HMH scores across PediCARE and usual supportive care arms on the ordinal scale from 0 to 4 using a chi-square test.