NCT05054413

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for all trials

Timeline
50mo left

Started Apr 2021

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress56%
Apr 2021Aug 2030

First Submitted

Initial submission to the registry

March 21, 2021

Completed
25 days until next milestone

Study Start

First participant enrolled

April 15, 2021

Completed
5 months until next milestone

First Posted

Study publicly available on registry

September 23, 2021

Completed
8.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2030

Last Updated

May 26, 2026

Status Verified

May 1, 2026

Enrollment Period

9.3 years

First QC Date

March 21, 2021

Last Update Submit

May 22, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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.

    through study completion, an average of a year.

Study Arms (1)

Observational (questionnaire)

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

Other: Questionnaire Administration

Interventions

Complete questionnaires

Observational (questionnaire)

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Participants with board certification in Radiation Oncology, Radiation Physics, Urology, and/or Medical Oncology

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

M D Anderson Cancer Center

Houston, Texas, 77030, United States

RECRUITING

Related Links

MeSH Terms

Conditions

Hematologic Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsHematologic DiseasesHemic and Lymphatic Diseases

Study Officials

  • Amy C Moreno

    M.D. Anderson Cancer Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 21, 2021

First Posted

September 23, 2021

Study Start

April 15, 2021

Primary Completion (Estimated)

August 1, 2030

Study Completion (Estimated)

August 1, 2030

Last Updated

May 26, 2026

Record last verified: 2026-05

Locations