Piloting Y-AMBIENT: A Quality of Life Intervention for Young African American Breast Cancer Survivors

Stopped early · Not applicable

Conditions studied: Breast Cancer, Anatomic Stage I Breast Cancer AJCC v8, Anatomic Stage IA Breast Cancer AJCC v8, Anatomic Stage IB Breast Cancer AJCC v8, Anatomic Stage II Breast Cancer AJCC v8, Anatomic Stage IIA Breast Cancer AJCC v8, Anatomic Stage IIB Breast Cancer AJCC v8, Anatomic Stage III Breast Cancer AJCC v8, Anatomic Stage IIIA Breast Cancer AJCC v8, Anatomic Stage IIIB Breast Cancer AJCC v8, Anatomic Stage IIIC Breast Cancer AJCC v8, Prognostic Stage I Breast Cancer AJCC v8, Prognostic Stage IA Breast Cancer AJCC v8, Prognostic Stage IB Breast Cancer AJCC v8, Prognostic Stage II Breast Cancer AJCC v8, Prognostic Stage IIA Breast Cancer AJCC v8, Prognostic Stage IIB Breast Cancer AJCC v8, Prognostic Stage III Breast Cancer AJCC v8, Prognostic Stage IIIA Breast Cancer AJCC v8, Prognostic Stage IIIB Breast Cancer AJCC v8, Prognostic Stage IIIC Breast Cancer AJCC v8

In brief

The purpose of this two-arm pilot RCT is to evaluate processes and preliminary outcomes of a targeted QOL intervention vs. an attention control among young AA survivors post-treatment for early (I-II) \& late (III) stage breast cancer.

Key facts

Study ID

NCT05452681

Run by

University of Alabama at Birmingham

People needed

27

Starts

2022-06-01

Expected to finish

2025-12-31

Last updated by the study team

2026-05-07

Who can join

Age: 18 and older, up to 44. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Biologically born women
• Self-identify as AA
• Are aged 18 to 44 years on study entry
• Are diagnosed with breast cancer stage I-III
• Have completed treatment with chemotherapy and/or radiation for stage I-III breast cancer prior to study entry
• Are English- speaking
• Have telephone and internet access

You may not qualify if…

• Participation in formal survivorship navigation programs because they are associated with improved health- related outcomes, which could be a confounder

Where it is running

• Ohio State University Comprehensive Cancer Center — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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