Recruiting

Breast Cancer Awareness

Sponsor:

Mayo Clinic

Code:

NCT07644702

Conditions

Breast Carcinoma

Eligibility Criteria

Sex: Female

Age: 50 - 70+

Healthy Volunteers: Not accepted

Interventions

Educational Intervention

Patient Navigation

Supportive Care

Study Details

Brief summary:

This clinical trial tests how well the Women's Engagement for Cancer Awareness, Resources, and Education (WE-CARE) community health forums work to increase breast cancer screening and clinical trial participation for rural and low income women. Despite advances in breast cancer diagnosis and treatment in the past decade, rural-dwelling and underserved women, and Black, Indigenous, and people of color continue to experience low rates of breast cancer screening. Since the survival rate for breast cancer is largely dependent on stage at which it is diagnosed, later stage breast cancer is correlated to a poorer prognosis and higher mortality rate. The WE-CARE community health forms address structural barriers through culturally tailored educational sessions on breast cancer risk, screening and clinical trials, survivor storytelling to humanize cancer and research and patient navigation to facilitate mammogram screening and address barriers. The WE-CARE community health forums may be an effective way to increase breast cancer screening and clinical trial participation for rural and low income women.

Conditions

Breast Carcinoma

Study ID

NCT07644702

Start date

Jan 5, 2026

Status verified date

Jun, 2026

Completion date

Jan 30, 2028

Anticipated

Primary completion date

Jan 30, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 50 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Female
  • Be between the ages of 50 and 74 years
  • Have no prior history of breast cancer screening (i.e., who have either never received a mammogram or have not had one in the past five years)
  • Reside in a rural community in Wisconsin or belong to low income (self-reported)
  • Be able to speak and understand English or Spanish
  • Be willing and able to provide informed consent

Exclusion Criteria:

  • Women who have received a mammogram within the past five years
  • Have a current or prior diagnosis of breast cancer
  • Are currently undergoing treatment for any active malignancy
  • Have cognitive or psychiatric impairments that, in the judgment of the study team, would preclude meaningful participation

Study Design

Enrollment

50 participants

Anticipated

Intervention Model

Single group

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

experimental: Health services research (WE-CARE forum)

Patients attend a WE-CARE community forum, over 2 hours. At the forum, patients attend educational sessions on breast cancer risk, screening and clinical trials as well as survivor storytelling sessions by community companions who have participated in clinical research for breast cancer. Patients also receive navigation support to facilitate mammography, address barriers, support scheduling, coordinate follow-up, and provide real-time guidance on screening and matching with clinical trials or registries.

Interventions

Educational Intervention

Attend education sessions at WE-CARE forum

Patient Navigation

Receive navigation support

Supportive Care

Attend storytelling sessions at WE-CARE forum

Primary outcome measure

  • Recruitment yield [ Time Frame: At time of forum ]
  • Exposure reach (community level reach) [ Time Frame: At time of forum ]
  • Retention [ Time Frame: From baseline to 3 months ]
  • Perceived participant satisfaction [ Time Frame: Immediately following completion of forum ]
  • Perceived barriers to engagement and community impact [ Time Frame: Immediately following completion of forum ]
  • Perceived facilitators to engagement and community impact [ Time Frame: Immediately following completion of forum ]
  • Perceived acceptability - AIM [ Time Frame: Immediately following completion of forum ]
  • Perceived appropriateness - IAM [ Time Frame: Immediately following completion of forum ]
  • Perceived feasibility - FIM [ Time Frame: Immediately following completion of forum ]

Central Contacts and Locations

Central contacts

Stephanie Larson

715-838-1976

Locations

Mayo Clinic Health System-Eau Claire Clinic

Recruiting

Eau Claire, Wisconsin, United States, 54701

Contacts

Stephanie Larson

715-838-1976

Principal Investigator:

Pravesh Sharma, MD

More Information

Sponsor

Mayo Clinic

Last update posted

Jun 12, 2026

Last verified

Jun, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Mayo Clinic on 2026-06-12.