Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07217262

Proactive Costs of Care Study

Led by Cedars-Sinai Medical Center · Updated on 2026-02-10

36

Participants Needed

1

Research Sites

66 weeks

Total Duration

On this page

Sponsors

C

Cedars-Sinai Medical Center

Lead Sponsor

M

Merck Sharp & Dohme LLC

Collaborating Sponsor

AI-Summary

What this Trial Is About

The Proactive Costs of Care intervention is an educational intervention designed to help patients deal with the cost of cancer care. The main goal of this trial is to evaluate whether the Proactive Costs of Care intervention can be successfully delivered to cancer patients who are starting a new treatment and their caregivers by looking at how many participants complete the intervention. The other questions the trial aims to answer are whether the intervention can: * Improve confidence in solving problems related to costs of care * Reduce distress related to finances Participants will complete the Proactive Costs of Care intervention, which is an approximately 30-minute one-time session with a lay educator reviewing the Proactive Costs of Care Guide and Cost Tracker. The intervention can be completed in person, by video, and by phone. Participants will also complete two surveys- one to be completed before the intervention and one to be completed 3 months after the intervention.

CONDITIONS

Official Title

Proactive Costs of Care Study

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals 18 years old or older
  • Diagnosed with gynecologic cancer
  • On active systemic therapy within 30 days of enrollment
  • Receiving treatment at Cedars-Sinai Medical Center
  • Can speak, read, and understand English
  • Caregivers to eligible patients
Not Eligible

You will not qualify if you...

  • Patients with records flagged as "break the glass" or "research opt out"
  • Cannot speak, read, or understand English
  • Unwilling to participate in the intervention or complete surveys

AI-Screening

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Trial Site Locations

Total: 1 location

1

Cedars-Sinai Medical Center

Los Angeles, California, United States, 90048

Actively Recruiting

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Research Team

S

Shu-Fan Chen, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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