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NCT05127850 | Active, not recruiting | Prostate Cancer


MENCORE-2: Audio Recordings to Improve Decision-making in Advanced Prostate Cancer
Sponsor:

University of California, San Francisco

Brief Summary:

This is a single-arm hybrid implementation trial of men with metastatic castrate-resistant prostate cancer (mCRPC) involving a patient-administered mobile app for consultation audio recordings.

Condition or disease

Prostate Cancer

Metastatic Prostate Cancer

Metastatic Castration-resistant Prostate Cancer

Intervention/treatment

Consultation audio recording app

Phase

Not Applicable

Detailed Description:

PRIMARY OBJECTIVE: 1. To evaluate change in participant informed decision-making after provision of a consultation audio recording application. SECONDARY OBJECTIVES: Reach. To evaluate the percentage of invited participants who enroll. Reasons for not enrolling will be assessed. Adoption. To evaluate the percentage of providers who agree to be recorded. Adoption. To evaluate the percentage of participants who create an audio recording. Adoption. To evaluate the percentage of participants who listen to the audio recording or read its automatically generated transcript. Implementation. To evaluate the percentage of participants who report receiving instructions on how to record. To evaluate participant-reported shared decision-making effort. To evaluate whether participant-reported anxiety changes after provision of a consultation audio recording app. To evaluate barriers, facilitators, and experiences of recording app use, particularly in the context of treatment decision-making by conducting participant interviews, provider surveys, and interviews with providers. Treatment received. EXPLORATORY OBJECTIVES: To evaluate whether provision of a consultation audio recording app improves participant-reported knowledge retention of docetaxel. To evaluate accuracy of app auto-generated transcription. To evaluate degree of provider decision support and communication skills. Participants are set up with an application prior to the first physician visit and then followed-up 7 days, 28 days and 60 days after their physician encounter.

Study Type : Interventional
Estimated Enrollment : 51 participants
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: Mhealth ElectroNic COnsultation REcording (MENCORE-2): an Implementation Trial to Improve Informed Treatment Decision-making in Men With Advanced Prostate Cancer
Actual Study Start Date : March 22, 2022
Estimated Primary Completion Date : February 18, 2024
Estimated Study Completion Date : April 30, 2024
Arm Intervention/treatment

Experimental: Consultation audio recording

Instructions on installation and detailed use of chosen application will be provided before an upcoming oncology visit. Research staff will contact the participant and encourage a "practice" recording session. 15-30 minutes prior to the consultation, research staff will send an anonymous text message to the participants' mobile device with a reminder to record the visit. Three days after the consultation, research staff will send an anonymous text reminder message to the participants' mobile device to listen to the recording.

Behavioral: Consultation audio recording app

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: Male
Accepts Healthy Volunteers: No
Criteria
Inclusion Criteria
  • Metastatic castration-resistant prostate cancer (mCRPC) with progression per any Prostate Cancer Working Group 3 (PCWG3) criterion (Prostate-specific antigen (PSA), clinical, or radiographic)
  • Has never received any chemotherapy for prostate cancer.
  • Current or prior receipt of at least one androgen-signaling inhibitors (ASI) (abiraterone, enzalutamide, apalutamide, or darolutamide), with progression on it.
  • Eligible for docetaxel chemotherapy at any dose level (treating provider's discretion).
  • Has an upcoming genitourinary (GU) medical oncology appointment (in-person, telephone, or Zoom video visit) at University of California, San Francisco (UCSF) within 7-60 days of enrollment, during which next-line treatment options are anticipated to be discussed (treating provider's discretion).
  • 18 years of age or older.
  • Able to read, speak, and write in English (the application is in English only)
  • Has access to and ability to use an iOS or Android smartphone or tablet.
  • For video visits only: has access to and ability to use a second device (e.g., desktop, laptop, smartphone, tablet, etc.) that will run a Zoom video visit.
  • Patient's provider of the upcoming appointment in #5 agrees to be recorded.
  • Inclusion criteria (provider participants)
    • 1. UCSF GU medical oncology providers (medical doctor (MD), nurse practitioner (NP), or physician's assistant (PA)), regardless of whether their patient was enrolled
    Exclusion Criteria
    • Lack of decision-making capacity to provide consent to this trial.
    • Uncorrectable hearing or visual impairment hindering the ability to perform necessary tasks in the trial.
    • Any neurocognitive or psychiatric disorder hindering the ability to perform necessary tasks in the trial.
    • Prior participation in Mobile Health ElectroNic COnsultation REcording (mENCORE) (participants have already received the intervention).

MENCORE-2: Audio Recordings to Improve Decision-making in Advanced Prostate Cancer

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MENCORE-2: Audio Recordings to Improve Decision-making in Advanced Prostate Cancer

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Locations


Not yet recruiting

United States, California

University of California, San Francisco

San Francisco, California, United States, 94143

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