Creating guidelines for prostate cancer care using expert opinions

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to establish consensus guidelines for key clinical elements in prostate cancer care through a remote Delphi method. A panel of certified experts in relevant fields will participate in multiple rounds of questionnaires to identify essential data elements for standardized reporting in electronic health records. The goal is to enhance the management of prostate cancer patients from diagnosis through survivorship by ensuring consistency in the information recorded. The study emphasizes the importance of expert input in developing these guidelines to improve patient care.

Why it matters

Who can join: the full rules

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

Where it's running

• M D Anderson Cancer Center
  Houston, Texas, United States Recruiting

Study contacts

• Principal investigator: Amy C Moreno — M.D. Anderson Cancer Center
• Study coordinator: Amy C Moreno
• Email: akmoreno@mdanderson.org
• Phone: 713-745-4590

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.