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Formulating Expert Consensus Guidelines in Cancer Care Using the Delphi Method

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status

Enrolling

Conditions

Hematopoietic and Lymphoid Cell Neoplasm
Malignant Solid Neoplasm

Treatments

Other: Questionnaire Administration

Study type

Observational

Funder types

Other

Identifiers

NCT05054413
NCI-2021-01928 (Registry Identifier)
2020-1096 (Other Identifier)

Details and patient eligibility

About

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.

Full 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.

Enrollment

10 estimated patients

Sex

All

Ages

21+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

10 participants in 1 patient group

Observational (questionnaire)
Description:
Participants complete 3-4 rounds of questionnaires over 20-30 minutes each over 2 weeks.
Treatment:
Other: Questionnaire Administration

Trial contacts and locations

1

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Central trial contact

Amy C Moreno

Data sourced from clinicaltrials.gov

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