Nutrition, Vision, and Cognition in Sport Study: Beef

NCT ID: NCT04427852

Last Updated: 2025-09-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-01-20

Study Completion Date

2021-06-01

Brief Summary

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The purpose of this study is to determine whether a 30 day beef intervention can improve peak cognitive performance in young, normally menstruating adult women. The control group will consume a daily portion of macronutrient equivalent vegetable source of protein.

Detailed Description

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The purpose of the Nutrition, Vision, and Cognition in Health Sport: Beef (IONSport-Beef) study is to conduct a randomized controlled trial to evaluate beef as a nutritional intervention to optimize visual cognitive training performance in generally healthy, normally menstruating women. Female subjects of reproductive age (18-40) will be randomly placed in one of two dietary treatment groups: one serving of beef per day for 30 days or a non-meat protein replacement control. Cognitive performance will be measured in 15 training sessions over 10 days using the sophisticated NeuroTrackerâ„¢ CORE (NT) 3-Dimensional (3D) software program. It is hypothesized that women consuming 1 serving of beef per day for 30 days will have the highest plasma levels of the beef rich nutrients and demonstrate the highest visual cognitive performance and improvement as compared to the no beef control.

Conditions

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Cognitive Change Nutrient Deficiency Nutritional Anemia Visual Spatial Processing Diet, Healthy Diet; Deficiency Dietary Deficiency Dietary B12 Deficiency Dietary Zinc Deficiency Dietary Vitamin B12 Deficiency Anemia Dietary Deficiency of Selenium and Vitamin E

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Study participants will be randomized to either one serving of beef or a macronutrient equivalent "veggie patty" per day for 30 days.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

note on masking: The title of the study presented to participants is "IONsport: Women and Protein" and the funding source is withheld to mask from participants our underlying hypothesis. It is open label in the sense that they know what they are eating.

Study Groups

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30 day Beef consumption

One serving of beef is consumed each day for 30 days.

Group Type EXPERIMENTAL

30 day Daily consumption of 1 serving of beef

Intervention Type DIETARY_SUPPLEMENT

Beef patty will replace one of the participants protein servings each day for 30 days. Each serving is 114 grams of 90% lean ground sirloin given to participants as an uncooked frozen patty.

30 day Veggie Patty consumption

One serving (1 patty) of a vegetable based protein source is consumed each day for 30 days. The weight of the food, total calories, grams of protein, and total fat are the same as the beef serving.

Group Type PLACEBO_COMPARATOR

30 day Daily consumption of 1 serving of the vegatable protein source

Intervention Type DIETARY_SUPPLEMENT

Veggie patty will replace one of the participants protein servings each day for 30 days. No beef will be consumed during this period. The veggie patty is commercially available Morningstar veggie burger and is given to participants in commercial packaging as a frozen precooked patty.

Interventions

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30 day Daily consumption of 1 serving of beef

Beef patty will replace one of the participants protein servings each day for 30 days. Each serving is 114 grams of 90% lean ground sirloin given to participants as an uncooked frozen patty.

Intervention Type DIETARY_SUPPLEMENT

30 day Daily consumption of 1 serving of the vegatable protein source

Veggie patty will replace one of the participants protein servings each day for 30 days. No beef will be consumed during this period. The veggie patty is commercially available Morningstar veggie burger and is given to participants in commercial packaging as a frozen precooked patty.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

1. 18-40 year old female
2. Eumenorrheic

Exclusion Criteria

1. Neuroactive medications such as Ritalin, Adderall, antidepressants etc
2. Dietary supplements
3. Iron intake above 15mg/day
4. Protein intake above 1.5 g/kg/day
5. More than 1 mild concussion lifetime or 1 mild concussion within the last 12 months
6. History of affective disorder
7. Visual impairments uncorrected by glasses
8. Amenorrhea or dysmenorrhea
9. Currently being treated for anemia
10. \>3 servings of beef per week
11. \<20 BMI or BMI \>35
12. Consume \>100mg caffeine/day (\>1 cup of coffee or soda)
13. \<1 hour/week physical activity, \>4 hours/week vigorous activity
14. Depression score \>18 (Beck Depression Inventory)
15. \<20 Kcal/kg/day
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Texas A&M University

OTHER

Sponsor Role lead

Responsible Party

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Steven E.Riechman, PhD, MPH

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Steve Riechman, PhD

Role: PRINCIPAL_INVESTIGATOR

Texas A&M University

Locations

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Texas A&M University

College Station, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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M1803347

Identifier Type: -

Identifier Source: org_study_id

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