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Clinical Trials/NCT05054413
NCT05054413RecruitingNot Applicable

Key Elements for Standardized Reporting in Prostate Cancer Management: An Expert Delphi Consensus Study

M.D. Anderson Cancer Center2 sites in 1 country10 target enrollmentStarted: April 15, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
10
Locations
2
Primary Endpoint
To establish a standardized methods to report key data in electronic health records to better manage cancer patients at time of diagnosis, treatment, follow up, and into survivor-ship.

Study Overview

Brief Summary

This study formulates consensus agreement on clinical key elements related to prostate cancer care that are critical for standardization and global reported using a robust Delphi technique, completely remote and electronic. The goal of this survey study is to have a panel of specialty-specific experts create a consensus agreement on a minimum set of key data elements for use in standardized reports. These recommendations would be used to develop standardized methods to report key data in electronic health records to better manage cancer patients at time of diagnosis, treatment, follow up, and into survivorship.

Detailed Description

PRIMARY OBJECTIVE:

I. To formulate consensus agreement on a minimum set of clinical key elements that should be included in standardized reports in electronic health records when managing patients with prostate cancer.

OUTLINE:

Participants complete 3-4 rounds of questionnaires over 20-30 minutes each over 2 weeks.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age 21 and above
  • Board certification in Radiation Oncology, Radiation Physics, Urology, and/or Medical Oncology
  • Maintenance of an active practice that includes prostate cancer patients
  • English speaking

Exclusion Criteria

  • Medical providers that are not board certified in the professions and/or those who do not treat prostate cancer
  • Prisoners, children, and adults unable to consent to participation will also be excluded
  • No exclusions were made based on sex, age, racial/ethnic background, or pregnancy status

Outcomes

Primary Outcomes

To establish a standardized methods to report key data in electronic health records to better manage cancer patients at time of diagnosis, treatment, follow up, and into survivor-ship.

Time Frame: through study completion, an average of a year.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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