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Navigating Financial and Health-Related Social Needs in Adolescent and Young Adult Cancer Survivors (AYA-NAV)

Navigating Financial and Health-Related Social Needs in Adolescent and Young Adult Cancer Survivors (AYA-NAV): A Digital Intervention Pilot Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06950983
Acronym
AYA-NAV
Enrollment
120
Registered
2025-04-30
Start date
2025-07-23
Completion date
2027-07-31
Last updated
2026-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer in Adolescence

Keywords

Cancer, Adolescents, Young adults, Financial needs, Social needs

Brief summary

Aim 1: Refine the HRSN navigation model to integrate a digital platform (Findhelp.org) to meet the needs of AYAs. The investigators will conduct iterative co-design sessions with AYAs and caregivers to understand their views on the existing Findhelp.org website and the likely need for other human-to-human and digital strategies to augment platform engagement (e.g., text reminders) and to address vocational needs. Aim 2: Evaluate the feasibility and acceptability of the refined hybrid intervention that includes digital + person-to-person HRSN navigation. Aim 3: Explore the preliminary impact of the refined hybrid intervention, compared to elevated usual care (a one-time referral to FindHelp.org alone), on reduction in financial distress (AYA and caregiver) and on AYA global health (i.e., mental, social, physical).

Detailed description

Nearly 90,000 adolescent and young adults (AYA: defined by the National Cancer Institute \[NCI\] as age 15-39 years) are diagnosed with cancer annually in the United States (US), 85% of whom are expected to become long-term survivors. Compared to their peers, these survivors have an increased burden of chronic health conditions. AYAs also face devastating financial toxicity, defined as the negative personal financial impact of healthcare costs, resulting not only from the cost of care, but also from interrupted education, exclusion from the workforce, and developmental disruption in achieving or maintaining independence. In fact, AYA cancer survivors experience disproportionately higher rates of financial toxicity and unemployment, associated with poorer overall survival and bankruptcy, compared to older cancer survivors. Among AYA survivors, those with public insurance, who live in areas of high deprivation, and/or who are Black or Hispanic/Latino (hereafter Hispanic) have lower rates of 5- and 10-year survival, likely due in part to adverse social determinants of health (SDOH) and unmet health-related social needs (HRSN: financial strain, food insecurity, un/underinsurance, unstable housing, and suboptimal education). The research team has studied financial toxicity and HRSN among Spanish- and English-preferring AYAs and their caregivers to develop participant-informed interventions to address unmet HRSN. This study is pilot testing a needs navigation model, adapted from an adult-directed model, among Spanish- and English-speaking AYAs who screen positive for high financial toxicity or unmet HRSN and are receiving care at Columbia University Irving Medical Center (CUIMC) in New York City. This model includes tailored needs navigation delivered over 6 months by a community organization that provides telephone-based case management to people facing life-limiting illness. Though AYA participants are initially interested in this AYA-HRSN navigation model (consent rates \>85%), uptake and sustained engagement are rarely observed. During monthly check-ins with participants, investigators identified two gaps in the current model. First, AYAs do not perceive the model to be acceptable in addressing their needs because it is not accessible digitally. Findhelp.org is an established, digital network of local resources that can be leveraged to address this gap. Second, AYAs and caregivers request support to address educational and vocational needs, a resource not available through our community partner. Informed by these preliminary findings and given that AYAs are digital experts, the objective of this R21 proposal is to adapt the needs navigation model to a digital platform, while adding vocational navigation, to better engage AYAs and address their unmet HRSN. Using mixed methods, the investigators will refine the intervention (Aim 1) and conduct a randomized pilot study to measure its feasibility and acceptability (Aim 2) and compare the impact of the digital HRSN navigation intervention with elevated usual care (Aim 3). This study will enroll and randomize (1:1) 80 English- and Spanish-speaking AYAs who are within 6 months of completing curative-intent cancer treatment.

Interventions

BEHAVIORALAYA-NAV

Support for AYA and vocational navigation sessions from clinical team

Sponsors

Columbia University
Lead SponsorOTHER
National Institute of Nursing Research (NINR)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Focus groups for aim 1. Parallel study model for aim 2 and 3

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Aim 1: * AYAs (age 18-39) who have/had a diagnosis of cancer are eligible to participate. * English or Spanish-speaking Aim 2 and 3: * AYAs (age 15-39) who were diagnosed with cancer or began treatment for cancer within the past 6 months, or those who are still on first treatment for cancer (non-relapse) * English or Spanish-speaking * For AYAs who are \< 18 years, caregiver participation will be required; for AYAs \> 18 years, caregivers may co-participate if desired; the primary unit of focus is the AYA patient.

Exclusion criteria

* Dyad with caregiver or younger AYA that previously participated in study AAAU2405 or AAAY9477 * Unable to complete financial survey questions or contraindicated (as outlined in Protection of Human Subjects) * Dyad with younger AYAs who are enrolled on hospice or receiving other end-of-life care

Design outcomes

Primary

MeasureTime frameDescription
Recruitment rate (feasibility)Up to 6 monthsPercent eligible out of total screened
Consent rate (feasibility)Up to 6 monthsPercent consented out of eligible total
Retention rates (feasibility)Up to 6 monthsPercent of enrolled that completed the 6-month assessment
Comprehensive Score of Financial Toxicity (COST) scorebaseline, 6-monthsThe COST is a patient-reported outcome measure that describes the financial distress experienced by cancer patients. It is a 11-item questionnaire with a score range of 0-44. Lower COST values indicate higher toxicity. Higher scores indicate lower financial toxicity.

Secondary

MeasureTime frameDescription
Patterns of engagementUp to 6 monthsEngaged with an intervention component at least once
Implementation outcomes6 months12-item AIM/IAM/FIM (Acceptability of Intervention Measure; Intervention Appropriateness Measure; Feasibility of Intervention Measure). Each item gets a score of 1-5. A higher score indicates greater acceptability, appropriateness, or feasibility.
Patient-Reported Outcomes Measurement Information System (PROMIS) Global Mental Health MeasureBaseline, 6-monthsPROMIS Global Health measure. Quality of Life Measure (scale 1-5; higher number indicating better QoL)

Countries

United States

Contacts

CONTACTMelissa Beauchemin, PhD, MSN,CPNP-PC, CPO
mmp2123@cumc.columbia.edu212-342-4111
CONTACTRhea Khurana, BS
rk3320@cumc.columbia.edu9173970773

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 24, 2026