Time-Restricted Eating for Fatigue in Cancer Patients

(THYME Trial)

AK
Overseen ByAmber Kleckner, PhD
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: University of Maryland, Baltimore
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

Treatments for advanced and metastatic cancer can cause fatigue and accelerate the progression to frailty. There are few effective mitigation strategies for fatigue or frailty in chronic cancer in part because the underlying etiology and pathophysiology are not well understood. However, disruption of circadian rhythms is a mechanism that possibly underlies fatigue and other components of frailty. Time-restricted eating is a daily eating pattern that entails consuming food within a defined, consistent window (e.g., 10 hours) every day. When the eating window aligns with the daylight hours, it entrains circadian processes and modulates physiological regulation of whole-body metabolism. Stronger physiological regulation means that the body will better be able to respond to physiological perturbations such as standing up from lying down, walking vs. sitting still, and eating food, as well as sleep more efficiently and have more perceived energy during the day. It is also predicted that patients will be less vulnerable to the aging process. It is hypothesized that time-restricted eating can alleviate fatigue and slow the progression to frailty in older adults with cancer as a chronic condition via regulating circadian rhythms and improving physiological responsiveness. This project is a 12-week, two-arm, phase II randomized controlled trial comparing the effects of time-restricted eating (10 h daytime feeding/14 h fasting at night) vs. a nutrition counseling control intervention (no time component) on fatigue; 6- and 12-month follow-up time points are also planned. A total of 132 patients with prostate cancer or metastatic breast cancer will be recruited; eligible participants will be 55 years or older, consume food within a window that is \>12 h at baseline, and not be employed in night-shift work. They will be randomized 1:1, intervention: control. At baseline, 12 weeks (post-intervention), and 12 months, we will assess patient-reported fatigue (Aim 1); frailty via Fried's frailty criteria (Aim 2); and measures of circadian rhythms (i.e., rest-activity rhythm, urinary hormones) and physiological responsiveness (i.e., lying vs. standing blood pressure, sitting vs. walking heart rate, glucose tolerance, phosphocreatine recovery) (Aim 3, mechanistic aim). The time-restricted eating intervention is scalable and inexpensive, lending itself to accessibility for the vast majority of people living with cancer as a chronic condition. Data generated herein will be used to inform a larger, phase III multisite clinical trial testing the effects of time-restricted eating on fatigue and frailty among older adults living with cancer and further optimize interventions that entrain circadian rhythms and improve energy production.

Are You a Good Fit for This Trial?

This trial is for adults aged 55 or older with prostate cancer or metastatic breast cancer who eat over more than 12 hours a day and do not work night shifts. Participants should be experiencing fatigue or frailty related to their cancer.

Inclusion Criteria

Have a life expectancy of ≥1 year
I am 55 years old or older.
Have a body mass index (BMI) ≥18.5 kg/m^2
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Exclusion Criteria

Be employed in overnight shift work more than 1 day/week on average
I do not have any medical reasons that prevent me from having this treatment.
Have had time zone travel ≥2 time zones away within the last 4 weeks
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What Are the Treatments Tested in This Trial?

Interventions

  • Nutrition counseling
  • Time-restricted eating

Trial Overview

The study compares two groups: one follows time-restricted eating (eating only during a set 10-hour window each day), while the other receives standard nutrition counseling without any time limits. The goal is to see which approach better reduces fatigue and frailty over 12 weeks.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Time-restricted eatingExperimental Treatment2 Interventions
Group II: Time-unrestricted eatingActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Maryland, Baltimore

Lead Sponsor

Trials
729
Recruited
540,000+