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NCT05440929Recruiting

Evaluation of the Acceptability, Appropriateness, and Feasibility/Usability of a Metastatic Breast-cancer Specific Prognostic Calculator Among Clinicians

Source: ClinicalTrials.gov · Last updated 28 Sept 2026

Brief summary (registry, in English)

I this qualitative study, Investigators will conduct semi-structured interviews with clinicians that are involved in the care of patients with breast cancer to evaluate the acceptability, appropriateness, and feasibility/usability of a metastatic breast cancer-specific prognostic tool. These interviews will be conducted by the UNC CHAI Core and will continue until thematic saturation (estimated 10 participants). The investigators will code the qualitative data using emerging themes, guided by a well-established implementation science theory, the Consolidated Framework for Implementation Research (CFIR). The information gained from these studies will inform an implementation approach to increase the usability and acceptability of a novel prognostic tool to assist oncologists in the prognosis of patients with metastatic breast cancer.

Status (registry)
Recruiting
Study type
Observational
Enrollment
15 (estimated)
First submitted
21 Jun 2022
Start date
7 Jul 2022
Primary completion date
10 Aug 2027
Lead sponsor
UNC Lineberger Comprehensive Cancer Center
NCT number
NCT05440929

What you commit to

  • Study type: Observational
  • Planned participants: 15
  • From 7 Jul 2022 to the primary completion date, 10 Aug 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Non-English Speaking

Who the study is looking for

  • Verbal informed consent obtained to participate in the study.
  • Subject is willing and able to comply with study procedures based on the judgement of the investigator or protocol designee.
  • Physician, nurse practitioner, physician assistant, or nurse navigator
  • At least 6 months of experience in the clinical care of patients with metastatic breast cancer in the United States.

Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
University of North Carolina
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Chapel HillUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.