Cost Talk: Discussing Cancer Care Costs

  • STATUS
    Recruiting
  • participants needed
    200
  • sponsor
    Washington University School of Medicine
Updated on 19 February 2024
prostate specific antigen
cancer care

Summary

The purpose of this study is to investigate whether an encounter decision aid (used during a consultation) containing cost information about options, combined with clinician training about cost discussions and available financial resources, influence surgeon-patient cost conversations, referrals to address costs, patients' financial stress, and high-quality decision-making for patients with slow-growing prostate cancer.

Description

The study will use a stepped wedge design to evaluate the encounter decision aid. Each participating urologic surgeon will begin in the usual care arm of the study. Subsequently, the surgeons will be randomized to the intervention arm at staggered time points to undergo training and begin using the decision aid intervention with patients who are diagnosed with slow-growing prostate cancer. This study will consist of two aims. The first aim is to examine the use of an encounter decision aid with cost information on the presence and impact of out-of-pocket cost conversations. The investigators will train participating clinicians on how to use the decision aid intervention and available financial resources. With patient and clinician consent, the investigators will audio record clinical encounters and measure cost conversations using a previously-developed checklist to code transcripts derived from the audio recordings. Patients can still participate if they do not consent to audio recording as these topics will be assessed in the self-report survey after their clinic or virtual visit. The second aim will examine the impact of an encounter decision aid with cost information on high-quality decision-making. The investigators will collect a post-visit questionnaire from participating patients, including patient-reported measures of decisional conflict, decision regret, and the shared decision-making process. Participants will be sent a follow-up questionnaire 3 months after their initial study enrollment to assess decision regret and financial toxicity.

Details
Condition Malignant neoplasm of prostate, Prostatic disorder
Age 18-100 years
Treatment Option Grid Decision Aid
Clinical Study IdentifierNCT04397016
SponsorWashington University School of Medicine
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

At least 18 years of age
Visiting a participating urologist/urologic surgeon to discuss treatment options
Slow growing prostate cancer defined as Gleason score of 6 or 7 (3+4) and/or PSA (prostate-specific antigen) level less than 10ng/ml
Must be patients of one of the participating providers

Exclusion Criteria

Patients who cannot give informed consent due to cognitive or emotional barriers
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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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