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Recruiting NCT07018986

NCT07018986 The MIND-BC Study: MIND Diet for Breast Cancer Cognition

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Clinical Trial Summary
NCT ID NCT07018986
Status Recruiting
Phase
Sponsor H. Lee Moffitt Cancer Center and Research Institute
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2025-07-09
Primary Completion 2029-03

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
MIND DietUsual Diet

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 200 participants in total. It began in 2025-07-09 with a primary completion date of 2029-03.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Previously diagnosed with stage I-III breast cancer. * Able to speak and read English. * Able to consume foods orally. * \>18 years of age. * Able to provide informed consent. * Have no documented or observable psychiatric or neurological disorder that would interfere with study participation (e.g., schizophrenia). * Report 'somewhat' to 'very much' cognitive impairment in the past week (i.e., a score ≥ 2 on a 0-4 scale) that they attribute to cancer or its treatment. * Report a MIND diet score \< 10 (range 0 to 14, higher score equates to higher diet quality). * Willing to consume the MIND diet. * Completed adjuvant treatment 6 months to three years previously. Exclusion Criteria: * Not meeting all of the inclusion criteria.

Contact & Investigator

Central Contact

Crystal Bryant

✉ Crystal.Bryant@moffitt.org

📞 813-745-2168

Principal Investigator

Sylvia Crowder

PRINCIPAL INVESTIGATOR

Moffitt Cancer Center

Frequently Asked Questions

Who can join the NCT07018986 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07018986 currently recruiting?

Yes, NCT07018986 is actively recruiting participants. Contact the research team at Crystal.Bryant@moffitt.org for enrollment information.

Where is the NCT07018986 trial being conducted?

This trial is being conducted at Tampa, United States.

Who is sponsoring the NCT07018986 clinical trial?

NCT07018986 is sponsored by H. Lee Moffitt Cancer Center and Research Institute. The principal investigator is Sylvia Crowder at Moffitt Cancer Center. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology