Actively Recruiting
The MIND-BC Study: MIND Diet for Breast Cancer Cognition
Led by H. Lee Moffitt Cancer Center and Research Institute · Updated on 2026-02-05
200
Participants Needed
1
Research Sites
242 weeks
Total Duration
On this page
Sponsors
H
H. Lee Moffitt Cancer Center and Research Institute
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This fully, powered efficacy RCT, the MIND diet for Breast Cancer Cognition (MIND-BC), will evaluate the MIND diet in a rigorous, highly controlled academic cancer center. We will recruit breast cancer survivors reporting CRCI with a MIND diet score \< 8, based on a previously devised 14-item diet questionnaire designed to detect inadequate diet with respect to brain health (scores range from 0 to 14, with lower scores indicating a less adequate diet).14 Breast cancer survivors will have recently completed adjuvant treatment (i.e., 6 months to three years previously), to ensure that perceived cognitive impairment is likely chronic and due to cancer. To achieve maximal effect, the study consists of two 12-week phases 1) intervention phase, 2) maintenance phase.
CONDITIONS
Official Title
The MIND-BC Study: MIND Diet for Breast Cancer Cognition
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Previously diagnosed with stage I-III breast cancer
- Able to speak and read English
- Able to consume foods orally
- Older than 18 years of age
- Able to provide informed consent
- No documented or observable psychiatric or neurological disorder that would interfere with participation (e.g., schizophrenia)
- Report cognitive impairment in the past week with a score of 2 or higher on a 0-4 scale attributed to cancer or its treatment
- Have a MIND diet score less than 10 on a 0 to 14 scale
- Willing to consume the MIND diet
- Completed adjuvant treatment 6 months to three years previously
You will not qualify if you...
- Not meeting all of the inclusion criteria
AI-Screening
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Trial Site Locations
Total: 1 location
1
Moffitt Cancer Center
Tampa, Florida, United States, 33612
Actively Recruiting
Research Team
C
Crystal Bryant
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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