NCT04835012

Brief Summary

The goal of this study is to estimate the direct, causal impact of medical debt on health care utilization, mental health, and wellbeing of patients. The investigators will conduct a survey to measure the impact of the debt forgiveness on health care use, mental health, and wellbeing. The survey will be administered to approximately 17,000 subjects of a recent medical financial intervention. In that prior intervention, a non-profit charity, RIP Medical Debt, purchased and abolished medical debt for a randomly selected about 6,000 (out of the 17,000) individuals. In this current protocol, the investigators will administer the survey, and will compare surveyed outcomes of subjects who received and did not receive the intervention.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
15,008

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2020

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 9, 2020

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

March 27, 2021

Completed
12 days until next milestone

First Posted

Study publicly available on registry

April 8, 2021

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2021

Completed
Last Updated

April 30, 2026

Status Verified

April 1, 2026

Enrollment Period

1.1 years

First QC Date

March 27, 2021

Last Update Submit

April 28, 2026

Conditions

Keywords

Health Care UtilizationMental HealthDepressionAnxietySubjective WellbeingMedical Debt

Outcome Measures

Primary Outcomes (1)

  • 8-item Patient Health Questionnaire (PHQ-8) Depression Scale

    Scores on the 8-item Patient Health Questionnaire depression scale range from 0 to 24, with higher scores indicating greater severity of depression.

    An average of 12 months after the intervention.

Secondary Outcomes (9)

  • Received Needed Health Care

    An average of 12 months after the intervention.

  • Received Needed Rx

    An average of 12 months after the intervention.

  • 7-item Generalized Anxiety Disorder (GAD7) Scale

    An average of 12 months after the intervention.

  • Stress

    An average of 12 months after the intervention.

  • General Health

    An average of 12 months after the intervention.

  • +4 more secondary outcomes

Study Arms (2)

Treatment

Subjects in this "treatment" group had their medical debt forgiven by a non-profit charity, RIP Medical Debt. This protocol will administer a survey to measure subjects' health care utilization, mental health, and subjective well-being.

Other: Medical debt forgiveness

Control

No intervention was given to subjects in this "control" group. This protocol will administer a survey to measure subjects' health care utilization, mental health, and subjective well-being.

Interventions

A non-profit charity, RIP Medical Debt, bought and retired medical debt for individuals that were assigned to the treatment group.

Treatment

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

The study population is a probability sample drawn from population of individuals who owe medical debt held by FFAM, a debt collection agency.

You may qualify if:

  • Individuals ages 18 and over who owed medical debt to FFAM, a debt collections agency

You may not qualify if:

  • Excluded individuals who owed less than $500 in medical debt to FFAM
  • Excluded individuals with missing social security numbers

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Wesley Yin

Los Angeles, California, 90095, United States

Location

MeSH Terms

Conditions

Patient Acceptance of Health CareDepressionAnxiety DisordersPsychological Well-Being

Condition Hierarchy (Ancestors)

Treatment Adherence and ComplianceHealth BehaviorBehaviorBehavioral SymptomsMental DisordersPersonal Satisfaction

Study Officials

  • Wesley Yin, PhD

    University of California, Los Angeles

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

March 27, 2021

First Posted

April 8, 2021

Study Start

November 9, 2020

Primary Completion

December 31, 2021

Study Completion

December 31, 2021

Last Updated

April 30, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will share

We will make de-identified and restricted data available to the research community through portals such as the publicly accessible Inter-University Consortium for Political and Social Research (hosted by the University of Michigan). We will preserve the confidentiality of study participants and protect personal health information by stripping the data of personally identifying information and purging it of all personal health information, and any information that is sufficiently fine so that it could identify individuals. We will follow standard protocols, such as converting specific dates to relative dates or date intervals, and aggregating small cells. This will allow us to maximize the data available to researchers while strictly preserving confidentiality and privacy.

Shared Documents
SAP, ICF, ANALYTIC CODE
Time Frame
De-identified and confidential IPD will be made available by the on-line publication date of published research.
Access Criteria
Access will be limited to researchers for non-commercial uses. Users will also need to certify that no attempt will be made to re-identify participants from the de-identified data.

Locations