Lead Sponsor

University of Maryland, Baltimore

Collaborators

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

•Have completed adjuvant chemotherapy, surgery, and/or radiation for cancer, including chemotherapy for hematologic neoplasms, at least 2 months and not more than 2 years prior to enrolling,
•Have a baseline level of fatigue, as determined by reporting a score of 4 or higher for the question, "In the last week, how bad was your worst fatigue on a scale from 0-10?"
•Be able to speak and/or read and write in English,
•Be at least 18 years old,
•Own a smartphone,
•Be willing and able to adhere to study procedures, including use of a smartphone app, and
•Be able to provide informed consent.

•Already eat all their food within a window that is 10 h or shorter most (6/7) days of the week,
•Be underweight, as defined as a body mass index ≤18.5 kg/m2,
•Have surgery planned during the study duration,
•Have any contraindications to the proposed nutrition intervention as identified by their medical provider, their designee, or the study team (e.g., type 1 diabetes, risk for hypoglycemia, medication requirements, pregnancy, breastfeeding, recent history of an eating disorder),
•Be taking insulin, or
•Be on enteral or parenteral nutrition.

Related studies

NCT07287098 · Breast Neoplasms

NCT07670221 · Chemotherapy-Related Taste Alteration

NCT07669519 · Fatigue, Colon Cancer

NCT07668037 · Non-Small Cell Carcinoma of Lung, Immunotherapy, and more

NCT07666464 · Therapy, Pleural Infections

Time-Restricted Eating to Address Persistent Cancer-Related Fatigue