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Clinical Trials/NCT06611982
NCT06611982
Active, Not Recruiting
N/A

Guaranteed Income and Financial Treatment Trial

Meredith Doherty, PhD, LCSW3 sites in 1 country250 target enrollmentApril 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cancer
Sponsor
Meredith Doherty, PhD, LCSW
Enrollment
250
Locations
3
Primary Endpoint
Financial Toxicity
Status
Active, Not Recruiting
Last Updated
9 months ago

Overview

Brief Summary

The goal of this clinical trial is to learn if providing advanced cancer patients with $1000/month for 12 months will improve cancer outcomes. The main questions it aims to answer are:

To what extent does receiving $1000/month additional income reduce financial hardship? To what extent does receiving $1000/month additional income improve quality of life? Does receiving $1000/month additional income improve survival outcomes?

Participants will:

Receive $1000/month for 12 months Complete a survey every 3 months for 12 months If selected, participate in semi-structured interviews about their financial behaviors

Detailed Description

Cancer-related financial hardship (i.e., financial toxicity) has been associated with anxiety and depression, greater pain and symptom burden, treatment nonadherence, and mortality. Out-of-pocket healthcare costs and lost income are primary drivers of financial toxicity, however, income loss is a pronounced risk factor for cancer patients with low incomes. There has been little progress in developing an income intervention to alleviate financial toxicity cancer patients with low incomes. Unconditional cash transfers (UCT), or guaranteed income, have produced positive health effects in experiments with general low-income populations, but have not yet been evaluated in people with cancer. The Guaranteed Income and Financial Treatment (GIFT) Trial will use a two-arm randomized controlled trial to compare the efficacy of a 12-month UCT intervention providing $1000/month to treatment as usual on financial toxicity, health-related quality of life and treatment adherence in people with cancer who have low-incomes. The study will recruit 250 Medicaid beneficiaries with advanced cancer from two comprehensive cancer centers in Philadelphia, obtain informed consent, and randomize patients to one of two conditions: (1) $1,000/month UCT or (2) treatment as usual. Both arms will receive information on financial toxicity and the contact information for their hospital social worker or financial advocate upon enrollment. Participants will complete online surveys at baseline, 3, 6, 9, and 12 months from enrollment to collect patient-reported data on primary (i.e., financial toxicity, health-related quality of life, and treatment adherence) and secondary outcomes (i.e., anxiety, depression, food insecurity, housing stability). Social security records will be used to explore the effect on mortality at 2, 3, and 5 years post-enrollment. Linear mixed-models will be used to analyze all primary and secondary continuous outcomes over time and general estimating equations with a logit link and binary distribution for all binary outcomes over time. Differences between treatment and control groups and treatment effects will be determined using models that control for age, gender, race, baseline food security, baseline housing stability, and baseline ECOG. Findings from this study will have significant implications for the development and implementation of programs and policies that address the financial burden of cancer and other serious illnesses.

Registry
clinicaltrials.gov
Start Date
April 1, 2023
End Date
July 30, 2026
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Meredith Doherty, PhD, LCSW
Responsible Party
Sponsor Investigator
Principal Investigator

Meredith Doherty, PhD, LCSW

Assistant Professor

Abramson Cancer Center at Penn Medicine

Eligibility Criteria

Inclusion Criteria

  • Age = 18 or older
  • Newly diagnosed or recurrent advanced cancer (Stage 3 or 4)
  • Receiving chemotherapy or immunotherapy (with or without radiation) at one of the recruitment sites
  • Within 12 months of receiving systemic therapy and on surveillance at one of the recruitment sites
  • ECOG performance status of 1 - 2
  • A Pennsylvania Medicaid beneficiary
  • A Pennsylvania resident

Exclusion Criteria

  • Eligible for hospice (i.e. determined by provider to have a prognosis of 6 months or less) at time of randomization
  • Unable to communicate in English, Spanish, or Mandarin

Outcomes

Primary Outcomes

Financial Toxicity

Time Frame: 6 and 12 months from enrollment

COmprehensive Score for Financial Toxicity (COST)

Treatment adherence

Time Frame: 6 and 12 months from enrollment

Number of missed appointments in last 30 days

Secondary Outcomes

  • Health-related quality of life(6 and 12 months from enrollment)
  • Anxiety and Depression(6 and 12 months from enrollment)

Study Sites (3)

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