Actively Recruiting
The RolE of Prolonged Nightly faSTing to Improve Sleep and cOgnition in bREast Cancer Survivors
Led by Arizona State University · Updated on 2026-05-01
60
Participants Needed
1
Research Sites
93 weeks
Total Duration
On this page
Sponsors
A
Arizona State University
Lead Sponsor
M
Mayo Clinic
Collaborating Sponsor
AI-Summary
What this Trial Is About
The investigators are interested in finding out how Prolonged Nightly Fasting (PNF) and/or health education may impact health and cancer recovery for breast cancer patients and survivors.
CONDITIONS
Official Title
The RolE of Prolonged Nightly faSTing to Improve Sleep and cOgnition in bREast Cancer Survivors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years old or older
- Diagnosed with breast cancer at any stage
- At least 3 months past neoadjuvant or adjuvant chemotherapy (including maintenance or palliative therapy)
- Score of 30 or lower on the Patient Reported Outcome Measurement Information System Cognitive Function Short Form 8a
- Able to speak and understand English
- Have access to a computer and Wi-Fi
- Live in the United States
- Identify as female
- Willing and able to fully participate in the study
You will not qualify if you...
- Type 1 diabetes
- Currently enrolled in a formal diet or weight loss program
- History of bariatric surgery
- History of eating disorders
- Working night shifts
- Pregnant, breastfeeding, or trying to become pregnant
- Diagnosed with dementia, psychological, psychiatric, or neurological disorders
- Active brain or central nervous system disease
- Current or prior use of memory enhancing medications
- History or current brain radiation
- Frequently fasting for 12 or more hours every night
- History of hypoglycemia
- Depression screening score of 20 or greater on PHQ9 or any score other than 0 on question 9
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Arizona State University
Phoenix, Arizona, United States, 85004
Actively Recruiting
Research Team
J
Jen Project Coordinator
CONTACT
D
Dorothy Sears, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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