Proactive Costs of Care Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCedars-Sinai Medical Center

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Individuals 18 years old or older are included.

Individuals diagnosed with gynecologic cancer

On active systemic therapy within 30 days of enrollment

Receiving treatment at Cedars-Sinai Medical Center

Disqualifiers

Any patients whose records are flagged "break the glass" or "research opt out."

Cannot speak, read, or understand English

Not willing to participate in the intervention or complete surveys

Trial design

Design model

Single group

Treatments tested in this trial

  • Educational Intervention

    Behavioral

    Participants will receive the Proactive Costs of Care Guide that covers health insurance, employment, and finding personal and community support. They will also receive the Proactive Costs of Care Cost Tracker to help track medical costs. This one-time intervention can be completed in-person, by video, or by phone. A trained lay educator will spend approximately 30 minutes reviewing health insurance and discussing the 2-3 topics most relevant to the participant. All of the materials are available in a paper version or electronic version.

Treatment groups

36 Participants
are divided into 1 treatment group
Group A: Patient and Caregiver Arm of Proactive Costs of Care StudyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Participant Completion Rate of Educational Intervention

The number of participants who completed the intervention divided by the total number of participants who consented to the study

Time frame
From enrollment to 2 months

Secondary outcomes

1

Change in Self-Efficacy using PROMIS Self-Efficacy

Scores range from 10-50, with higher scores indicating more self-efficacy

Time frame
From intervention to 3 months
2

Change in financial distress using InCharge Financial Distress/Financial Well-Being Scale

Scores range from 1-10, with higher scores indicating less financial distress

Time frame
From intervention to 3 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Cedars-Sinai Medical Center

Lead sponsor

Merck Sharp & Dohme LLC

Collaborator

Foundation for Women's Cancers

Collaborator