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Clinical Trial Summary

The study will use a cross-sectional study design with a follow-up 2-arm randomized controlled trial with that has assessments at baseline, post-intervention (i.e., Week 12), and 3-months post-intervention (i.e., Week 24). The 2 arms are the 12-week intervention and a health education control among 60 Black breast cancer survivors.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06100263
Study type Interventional
Source University of Michigan Rogel Cancer Center
Contact Cancer AnswerLine
Phone 1-800-865-1125
Email CancerAnswerLine@med.umich.edu
Status Not yet recruiting
Phase N/A
Start date June 2024
Completion date December 2026

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