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Longitudinal Examination of Metabolic and Behavioral Correlates of Protein Sources

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Oklahoma State University

Status

Active, not recruiting

Conditions

Health Behavior

Treatments

Other: Beans/legumes
Other: Beef
Other: Meat analogue

Study type

Interventional

Funder types

Other

Identifiers

NCT06089460
IRB-22-297-STW

Details and patient eligibility

About

The purpose of this three-arm, pilot, randomized controlled trial is to examine the metabolic and behavioral impacts of consuming a diet characterized by protein from red meat, a meat analogue, or beans/legumes.

Enrollment

30 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-55 years of age
  • Willingness to consume any of the three protein sources
  • Willingness to stop consumption of any pre- or pro-biotic supplements
  • Willingness to follow a meal plan for four weeks

Exclusion criteria

  • Medical condition which precludes consumption of specific foods or whole food groups

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 3 patient groups

Beef
Experimental group
Description:
Individuals will be asked to consume beef as their only source of protein and follow an individualized meal plan for 4 weeks. Thereafter, they will be instructed to continue beef consumption with any other foods desired for 4 weeks.
Treatment:
Other: Beef
Meat analogue
Experimental group
Description:
Individuals will be asked to consume a commercial meat analogue product as their only source of protein and follow an individualized meal plan for 4 weeks. Thereafter, they will be instructed to continue the meat analogue consumption with any other foods desired for 4 weeks.
Treatment:
Other: Meat analogue
Beans/legumes
Experimental group
Description:
Individuals will be asked to consume beans/legumes as their only source of protein and follow an individualized meal plan for 4 weeks. Thereafter, they will be instructed to continue the bean/legume consumption with any other foods desired for 4 weeks.
Treatment:
Other: Beans/legumes

Trial contacts and locations

1

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Central trial contact

Ashlea Braun, PhD

Data sourced from clinicaltrials.gov

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