N/A
N=26
Characterizing and Addressing Financial Toxicity in AYAs With Cancer
Cancer in Adolescence
Bottom Line
View on ClinicalTrials.gov: NCT06072833 ↗Enrolled (actual)
26
Serious AEs
0.0%
Results posted
Mar 2026
Primary outcome: Primary: Number of Participants Who Completed the Intervention — 21 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Patient Financial Education / Navigation (Behavioral)
- Age
- Pediatric, Adult · 15+ yrs
- Sex
- All
- Sponsor
- Columbia University
- Primary completion
- Feb 2025
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Who Completed the Intervention |
21 | — |
| PRIMARY Number of Eligible Participants Who Received the Intervention |
23 | — |
| SECONDARY Comprehensive Score of Financial Toxicity (COST Measure) Score |
10.47; 16.53 | — |
Summary
The overall aims of this study are to address two important gaps in care for AYA cancer patients: 1) a financial toxicity measurement tool to assess AYA-specific needs, and 2) an intervention for mitigating financial toxicity in this population. Aim 1 involves adapting the COSTA measure and assessing the psychometric properties of the measure for a racial/ethnically diverse group of AYAs. Aim 2 and 3 involve the development and pilot testing of our novel financial education/ navigation (FE/FN) intervention.
Eligibility Criteria
Inclusion Criteria
AYA patient participants:
- Age 15 - 39 years old
- English or Spanish-speaking
- Diagnosed with cancer that required treatment within past 18 months
- Not currently on hospice care
Caregiver/financial partner participants:
- Parent or financially-responsible adult of non-adult AYA (<18 years) OR
- Identified by the AYA as caregiver, parent, or partner who is financially-responsible or a financial partner for AYA
Exclusion Criteria
- Unable to complete financial survey questions or contraindicated (as outlined in Protection of Human Subjects)
Data sourced from ClinicalTrials.gov (NCT06072833). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.