RecruitingPhase 2NCT06113016

Prevention of Frailty With Fisetin and Exercise in Breast Cancer Survivors

A Phase II Randomized Placebo-Controlled Study of Fisetin and Exercise to Prevent Frailty in Breast Cancer Survivors


Sponsor

Jonsson Comprehensive Cancer Center

Enrollment

164 participants

Start Date

Jul 23, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This phase II trial tests how well fisetin and exercise works in preventing frailty in breast cancer survivors. Fisetin is a natural substance found in strawberries and other foods and is available as a nutritional supplement. Nutritional supplements may be useful in eliminating cells that have undergone a process called senescence. Senescence is when a cell ages and permanently stops dividing but does not die. Over time, large numbers of these cells build up in tissues throughout the body and can release harmful substances that cause inflammation and damage nearby healthy cells. Giving fisetin may eliminate senescent cells in patients with breast cancer undergoing physical activity.


Eligibility

Sex: FEMALE

Plain Language Summary

Simplified for easier understanding

This study tests whether a natural plant compound called fisetin, combined with exercise, can prevent frailty and physical decline in postmenopausal women who have survived early-stage breast cancer. Frailty is a common side effect of cancer treatment that makes people weaker and more vulnerable. **You may be eligible if:** - You are a postmenopausal woman (either naturally or through treatment) - You have been diagnosed with early-stage breast cancer (stage I or II) - You have completed primary cancer treatment - You show signs of physical frailty or pre-frailty - You are 18 or older **You may NOT be eligible if:** - You are currently on cytotoxic chemotherapy - You have advanced (metastatic) breast cancer - You have certain other serious health conditions - You are taking certain medications that could interact with fisetin Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREBiospecimen Collection

Undergo collection of blood samples

OTHEREducational Intervention

Receive handout on physical activity

OTHERExercise Intervention

Receive individually tailored exercise intervention

DRUGFisetin

Given PO

OTHERPhysical Performance Testing

Ancillary studies

DRUGPlacebo Administration

Given PO

OTHERQuality-of-Life Assessment

Ancillary studies

OTHERQuestionnaire Administration

Ancillary studies


Locations(6)

UCLA Health Cancer Care in Alhambra

Alhambra, California, United States

UCLA Health Beverly Hills Primary & Specialty Care

Beverly Hills, California, United States

UCLA Health Burbank Primary & Specialty Care

Burbank, California, United States

UCLA / Jonsson Comprehensive Cancer Center

Los Angeles, California, United States

UCLA Health Primary Care in Marina del Rey

Marina del Rey, California, United States

UCLA Health Primary Care in Pasadena

Pasadena, California, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

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NCT06113016


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