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The Impact of Beef on Muscle Fatigue in Older Adults

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Indiana University

Status

Enrolling

Conditions

Older Adults
Muscle Weakness
Muscle; Fatigue, Heart

Treatments

Other: Vegetarian Diet
Other: Beef Diet

Study type

Interventional

Funder types

Other

Identifiers

NCT05860088
14941 (Other Identifier)

Details and patient eligibility

About

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.

Enrollment

30 estimated patients

Sex

All

Ages

60 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

30 participants in 2 patient groups

Beef Diet
Experimental group
Description:
Participants will be randomized to consume the beef diet for 8 weeks. After a 2-week period, participants will cross-over to consume the vegetarian diet for 8 weeks.
Treatment:
Other: Beef Diet
Vegetarian Diet
Experimental group
Description:
Participants will be randomized to consume the vegetarian diet for 8 weeks. After a 2-week period, participants will cross-over to consume the beef diet for 8 weeks.
Treatment:
Other: Vegetarian Diet

Trial contacts and locations

1

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Central trial contact

Cydne A Perry, PhD

Data sourced from clinicaltrials.gov

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