Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT05438511

A Formative Evaluation For Improving Breast Cancer Hormone Receptor Testing in Tanzania

Led by Memorial Sloan Kettering Cancer Center · Updated on 2025-08-05

85

Participants Needed

2

Research Sites

154 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to learn more about the challenges with breast cancer diagnosis in Tanzania and the support available to improve this process.

CONDITIONS

Official Title

A Formative Evaluation For Improving Breast Cancer Hormone Receptor Testing in Tanzania

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Breast cancer survivor, patient advocate, or key healthcare personnel involved in breast cancer care
  • Key healthcare personnel includes hospital and laboratory leaders, pathologists, laboratory scientists and technicians, oncologists, nurses, and surgeons with over 12 months of employment at the affiliated institution
  • Administrative or clinical involvement in delivering breast cancer care services
  • Age 18 years and above
  • Permanent resident or citizen of Tanzania
  • Participant or legally authorized representative willing and able to consent
  • Fluent in Swahili and/or English by self-report
  • Received breast cancer diagnosis for chart review participants
Not Eligible

You will not qualify if you...

  • Key stakeholders not residing at their institutions during data collection
  • Participants under 18 years of age for chart review

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Memorial Sloan Kettering Cancer Center (All Protocol Activities)

New York, New York, United States, 10065

Actively Recruiting

2

Muhimbili University of Health and Allied Sciences

Dar es Salaam, Tanzania

Actively Recruiting

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Research Team

D

Diana Ng, MD

CONTACT

T

T. Peter Kingham, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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