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Health Insurance Literacy Intervention for Cancer Survivors (CHAT-S Trial)

N/A
Waitlist Available
Research Sponsored by University of Utah
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 18 months
Awards & highlights

CHAT-S Trial Summary

This trial will test a virtual health insurance intervention to help young adult cancer survivors ages 26-39 gain knowledge, reduce financial burden, and improve surveillance for recurrence. Cost-effectiveness and budget impact analyses will be used to measure sustainability.

Who is the study for?
This trial is for young adult cancer survivors aged 26 to 45, who have been treated for breast, testicular, lymphoma, sarcoma, or colorectal cancer within the last year. Participants must speak English and be patients at specific Utah healthcare institutions.Check my eligibility
What is being tested?
The study tests a virtual health insurance navigation program called CHAT-S against usual care. It aims to improve insurance knowledge, reduce financial stress and enhance monitoring for cancer recurrence in participants through four sessions.See study design
What are the potential side effects?
Since this intervention involves education and counseling rather than medical treatment, traditional physical side effects are not expected. However, participants may experience emotional or cognitive discomfort while discussing sensitive topics like finances and health.

CHAT-S Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~18 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 18 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
COmprehensive Score for financial Toxicity (COST)
Health Insurance Literacy Measure
Health Insurance Literacy Measure (HILM)
Secondary outcome measures
Acceptability
COVID-19 Health Care Impacts
Cost related literacy
+6 more

CHAT-S Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: CHAT-SExperimental Treatment1 Intervention
CHAT-S consists of 4 bi-weekly 35-45 minute videoconferencing sessions with a patient navigator and a patient booklet on insurance, costs, and survivorship care.
Group II: Usual CarePlacebo Group1 Intervention
Usual care will consist of a resource list sent by the navigator.

Find a Location

Who is running the clinical trial?

University of UtahLead Sponsor
1,095 Previous Clinical Trials
1,775,285 Total Patients Enrolled
Intermountain HealthUNKNOWN
Massachusetts General HospitalOTHER
2,928 Previous Clinical Trials
13,198,055 Total Patients Enrolled

Media Library

CHAT-S Clinical Trial Eligibility Overview. Trial Name: NCT05829070 — N/A
Cancer Research Study Groups: CHAT-S, Usual Care
Cancer Clinical Trial 2023: CHAT-S Highlights & Side Effects. Trial Name: NCT05829070 — N/A
CHAT-S 2023 Treatment Timeline for Medical Study. Trial Name: NCT05829070 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is enrollment accessible to those over 55 years of age in this research study?

"This research study is seeking participants between the ages of 26 and 45."

Answered by AI

What criteria must I meet in order to qualify for participation in this clinical trial?

"Individuals between 26 and 45 years old who have a cancer diagnosis are eligible to participate in this study. This trial currently seeks approximately 300 participants for enrollment."

Answered by AI

Are there any open spots in this clinical research?

"According to the clinicaltrials.gov database, this experiment is not accepting volunteers at present time. The trial was first posted on July 1st 2023 and last revised on April 12th of the same year. Nonetheless, there are many other trials that require participants in lieu of this one; 526 studies are actively searching for subjects as we speak."

Answered by AI

What results are investigators hoping to observe from this trial?

"The primary measure of success in this trial will be the COST score, collected at Baseline. Secondary outcomes include Survivorship Care Receipt (gathering information on visits to both PCPs and Oncologists), Insurance Coverage (public/private policyholder details) and consequences of the pandemic on medical care access and finances (working status changes)."

Answered by AI
~200 spots leftby Oct 2027