The Impact of Beef on Muscle Fatigue in Older Adults

Last updated: April 30, 2026
Sponsor: Indiana University
Overall Status: Completed

Phase

N/A

Condition

Sarcopenia

Pain (Pediatric)

Polymyositis (Inflammatory Muscle Disease)

Treatment

Vegetarian Diet

Beef Diet

Clinical Study ID

NCT05860088
14941
  • Ages 60-85
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The goal of this controlled-feeding cross-over diet intervention is to compare a beef diet to a vegetarian diet on muscle fatigue in older adults. The aims are:

AIM 1: To test the hypothesis that muscle fatigue is attenuated in older adults consuming beef compared to older adults consuming a plant-based diet.

AIM2: To test the hypothesis that daily beef consumption improves biochemical indicators related to muscle fatigue.

Participants will be randomized to consume either a beef-based diet or vegetarian diet under controlled-feeding conditions for 8 weeks. After a 2-week washout period, participants will cross-over to consume either the beef diet or vegetarian diet for 8 weeks. Body composition and functional muscle outcomes will be measured during each 8-week feeding period. Blood samples will also be collected.

Eligibility Criteria

Inclusion

Inclusion Criteria

  • Ages 60-85 years

  • Ability to eat study diet meals for a total of 16 weeks

  • Ability to perform sit-to-stand chair and 6-minute walking tests based on results from PAR-Q questionnaire

  • Ability to provide fasted blood samples

  • Access to transportation

  • Willing to abstain from alcohol consumption and/or use illicit drug use for each 8-week intervention period

  • Ability to consent to participating in this study

  • English-speaking

  • Body mass index between 18.5 (normal) and 39.9 (obese) kg/m2

  • Minimum total body weight of 110 pounds

  • Non-anemia hemoglobin values: Females - >12.0 grams/dL; Men - >13.0 grams/dL

  • Able to ambulate without assistance

  • Physician's clearance for study participation (required prior to baseline testing)

Exclusion Criteria

  • Inability or refusal to sign the informed consent

  • Significant orthopedic limitations or other contraindications to exercise

  • Inability or refusal to perform muscle fatigue tests

  • Has dietary restrictions that prevent to consumption of beef, soy and/or wheat

  • Has liver or kidney complications

  • Live or work >25 miles from Bloomington study site or does not have transportation to the study site

  • Anticipate elective surgery during the study period

  • Diagnosis of progressive neurological disorders, musculoskeletal disorders, osteoarthritis, rheumatoid arthritis

  • Fracture or serious injury in the last 6 months

  • Stroke, revascularization, deep vein thrombosis, or pulmonary embolism in the past 12 months

  • Severe cardiovascular disease, uncontrolled systemic hypertension, chronic pulmonary disease

  • Plan to move residence or travel out of the local area during the study period

  • Current use of anti-coagulants (e.g. Coumadin or Warfarin)

  • Current use of prescription medications that affect heart rate or blood vessel dilation

  • Psychological or social characteristics that would interfere with their ability to fully participate in the study

Study Design

Total Participants: 24
Treatment Group(s): 2
Primary Treatment: Vegetarian Diet
Phase:
Study Start date:
July 10, 2023
Estimated Completion Date:
November 21, 2025

Connect with a study center

  • Indiana University Bloomington

    Bloomington, Indiana 47405
    United States

    Site Not Available

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