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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04258085
Other study ID # 2014P002688a
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2020
Est. completion date March 25, 2022

Study information

Verified date March 2022
Source Brigham and Women's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This observational study evaluates scale-up of a breast cancer early detection program in Rwanda that was initially piloted in a single district. Specifically investigators will examine patient volume, service delivery, loss-to-follow-up rates, and cancer detection rates noted following implementation of scale-up to 3 additional districts. For scaleup, breast cancer screening with CBE was added to a cervical cancer screening initiative, in a combined Women's Cancer Early Detection Program (WCEDP).


Description:

Investigators previously conducted a cluster randomized controlled trial of a clinician training program to facilitate prompt evaluation of women with breast symptoms in one rural district of Rwanda. Subsequently, Rwanda Biomedical Centre (RBC) has scaled up the curriculum in 3 districts, adapting the program to integrate CBE screening into a cervical cancer screening initiative. In this study, we will evaluate implementation of this combined screening initiative. Investigators will assess patient volume, services, diagnoses, and loss to follow up.


Recruitment information / eligibility

Status Completed
Enrollment 17379
Est. completion date March 25, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - All women and men who are evaluated for a breast concern or receive breast cancer screening through implementation of the nationally-led early detection programs Exclusion Criteria: - None

Study Design


Intervention

Other:
Early diagnosis program combined with electronic medical record
Implementation of early diagnosis approach targeting symptomatic women, combined with use of electronic medical record to facilitate documentation, patient tracking across levels of the health care system, and patient contact

Locations

Country Name City State
Rwanda Rwanda Biomedical Centre Kigali

Sponsors (4)

Lead Sponsor Collaborator
Brigham and Women's Hospital Breast Cancer Research Foundation, Partners in Health, Rwanda Biomedical Centre

Country where clinical trial is conducted

Rwanda, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cancer detection rate Proportion of patients presenting to health centers who are ultimately diagnosed with cancer; proportion of patients who receive biopsy who are ultimately diagnosed with cancer; proportion of individuals diagnosed with cancer who initially presented with versus without breast symptoms 2 years
Primary Loss to follow-up Rates of loss-to-follow up before and after implementation of electronic medical record in districts utilizing breast cancer screening approach; and loss to follow up in districts implementing early diagnosis approach and EMR one year
Primary Patient volume and services received Number of patients presenting at the health centers, district hospital and referral hospitals two years
Secondary Breast cancer stage Among women diagnosed with breast cancer, distribution of cancer stage among women who participated in the WCEDP. 2 years
Secondary Patients' costs out-of-pocket costs borne by patients while undergoing evaluation for an abnormal clinical breast exam 6 months
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