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Impact of Time Restricted Feeding on Daily Protein Requirements

Impact of Time Restricted Feeding on Daily Protein Requirements

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05610644
Enrollment
61
Registered
2022-11-09
Start date
2023-03-29
Completion date
2024-10-03
Last updated
2024-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nutrition Disorders in Old Age

Brief summary

The investigators aim to assess 24-hour protein kinetics at two different levels of protein intake: 0.8 (RDA) and 1.6g/kg/day (2RDA) during a normal dietary (TRAD) and a time restricted feeding (TRF) pattern in older adults.

Detailed description

The investigators aim to assess 24-hour protein kinetics at two different levels of protein intake: 0.8 (RDA) and 1.6g/kg/day (2RDA) during a normal dietary (TRAD) and a time restricted feeding (TRF) pattern in older adults. Individuals in the TRF pattern will only consume food during a 6-hour eating period and fast for the remaining 18 hours. Individuals in the TRAD pattern will consume isocaloric and isonitrogenous (RDA or 2RDA) diet but consume an all-beef-breakfast. Participants will consume oral stable isotopes to measure muscle protein synthesis (MPS), whole-body muscle protein breakdown (MPB), and whole-body protein balance (WBPB). Appropriate muscle, blood samples, and urine will be collected throughout a 24-hour metabolic trial following a 2-day controlled diet.

Interventions

OTHERisocaloric, isonitrogenous meals

Participants will eat prepared study meals for 3 days that have either the RDA of protein per day or twice the RDA of protein per day.

Sponsors

University of Arkansas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

1. Men and women ages 50-75 years. 2. BMI 20-30 kg/m2 inclusive. 3. Capable of providing informed consent. 4. COVID-19 negative and/or asymptomatic

Exclusion criteria

1. Subject who does not/will not eat animal protein sources. 2. Body mass index \<20 or \>30. 3. Hemoglobin \<10g/dL at screening. 4. Platelets \<150,000/uL at screening. 5. History of diabetes. 6. History of chemotherapy or radiation therapy for cancer in the 6 months prior to enrollment. 7. History of gastrointestinal bypass/reduction surgery. 8. History of a chronic inflammatory disease (e.g. what?) 9. Currently receiving androgen (e.g., testosterone) or anabolic (e.g., GH, IGF-I) therapy. 10. Currently using prescription blood thinning medications. 11. Currently using corticosteroid medications. 12. Unable or unwilling to suspend aspirin use for 7 days prior to Visit 3. 13. Unwilling to avoid using protein or amino-acid supplements during participation. 14. Subjects who are unwilling to fast overnight. 15. Participating in \>200 minutes/week of vigorous exercise and/or \>4 days/week of resistance training.

Design outcomes

Primary

MeasureTime frameDescription
Whole-body protein balance24 hoursVolume of net protein produced per unit of time

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026