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Not Yet Recruiting NCT07529353

Feasibility of 'Exercise for CAncer Patients and Healthy EAting Timeframes' .

Conditions: Breast Cancer, Cancer Related Fatigue

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 20
Sponsor: University of Rochester

Location: Wilmot Cancer Institute Rochester New York

Summary

This study evaluates the feasibility and preliminary effects of a home based exercise and activity program for individuals with cancer. Participants will engage in a structured intervention designed to support physical activity and symptom management. The study will assess changes in patient reported outcomes, functional measures, and overall adherence to the program. Findings will help determine whether this approach is practical and potentially beneficial for improving health related outcomes in this population.

Eligibility Criteria

Inclusion Criteria: * Must be aged 18 years or older * Must have a confirmed diagnosis of breast cancer (stage I-IIIC) * Must have completed adjuvant chemotherapy, surgery, and/or radiation for cancer at least 2 - 120 months prior to enrolling, * Must be prescribed adjuvant endocrine therapy, * Must have a baseline level of fatigue, as determined by reporting a score of 4 or higher on the Symptom Inventory * Must have a body mass index greater than or equal to 25 kg per meter squared * Must have the ability to ambulate independently * Must be willing and able to participate in home-based exercise and eating timeframe intervention * Must have the ability to read and understand the English language, Exclusion Criteria: * Must not have metastatic or recurrent breast cancer * Must not be currently receiving chemotherapy or radiation therapy * Must not have a medical condition that would preclude safe participation in intervention or study procedures * Must not be pregnant, or planning to become pregnant during the study period * Must not be in the active or maintenance stage of exercise behavior as assessed by the Exercise Stages of Change Short Form, * Must not have any condition that in the opinion of the investigator would interfere with participation or safety * Must not be currently using, or plan to initiate use of prescription or over-the-counter weight-loss medications

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07529353). StuddyBuddy aggregates publicly available trial information.