Breast Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 18 years or older
- People who have a confirmed diagnosis of breast cancer or Ductal Carcinoma In Situ (DCIS), which is an early form of breast cancer found in the milk ducts
- People who currently identify their gender as a woman or female
- People who were assigned female sex at birth
- People who are experiencing at least one barrier to getting healthcare, as identified by a social needs screening tool used in the trial
- People who understand the research nature of this study and are willing to give verbal consent to take part before any study activities begin
Who may not be able to join:
- People who do not have a suspected or confirmed diagnosis of breast cancer or Ductal Carcinoma In Situ (DCIS)
- People who have previously been diagnosed with any type of cancer
- People who were assigned male sex or intersex sex at birth
- People who are unwilling or unable to follow the requirements of the trial
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Kathryn Glaser, Roswell Park Comprehensive Cancer Center
Phone: 716-845-7637
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Enrollment rate; Reasons for refusal; Retention Rate; Reasons for discontinuation
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.