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Improving physical fitness and cognition with a nutritional intervention

Enhanced physical and cognitive performance in active duty airmen: evidence from a randomized multimodal physical fitness and nutritional intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN96342002
Enrollment
200
Registered
2020-07-28
Start date
2016-01-15
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

Optimization of human performance in United States Air Force airmen Nutritional, Metabolic, Endocrine

Interventions

The intervention is a two-arm trial, with one group receiving a nutritional beverage and physical fitness intervention and the other group receiving a placebo beverage and the same physical fitness in

Sponsors

University of Illinois at Urbana Champaign
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Active-duty Air Force status 2. Commit to study participation for 14 consecutive weeks 3. At least 18 but no older than 45 to minimize the risk of physical injury or cardiovascular occurrence due to the study’s required fitness activity

Exclusion criteria

Exclusion criteria: Study participants shall not: 1. Have a Department of Defense medical profile for mental and/or physical function limitation nor have a pregnancy profile 2. Be currently be taking prescription blood pressure medication 3. Take herbal dietary supplements, performance supplements or any other substance that contained ingredients that might affect cardiovascular response with exercise one week before study participation begins 4. Have a musculoskeletal injury that would limit their ability to engage in heavy resistance training and aerobic exercise 5. Have cardiovascular or respiratory disease that would limit their ability to engage in heavy resistance training and aerobic exercise

Design outcomes

Primary

MeasureTime frame
Primary fitness measures, all measured at both pre- and post-intervention (12 weeks): R/L means an average of both the Right and Left side of the body 1. Abdominal circumference (inches), measured using a tape measure 2. Sled Push & Pull R/L (seconds) measured by pushing (15 yds) and pulling (15 yds) a 140 lb sled twice 3. Rotation Smash Ball R/L (inches), measured distance thrown of a heavy medicine ball 4. Weight (pounds), measured with a scale 5. Wingate Upper Body (Watts/kg) measured using an arm crank with fixed resistance for 30 seconds 6. Body fat (% body weight) measured using DEXA overall and segmented body composition 7. Modified Illinois Agility (seconds) measured by quickly completing a weaving running course 8. Pull-ups (1 minute to complete as many as possible) 9. Push-ups (1 minute to complete as many as possible) 10. Sit-ups (1 minute to complete as many as possible) 11. Standing long jump (inches), best of three jumps from a 2-foot static position 12. VO2 Max (mL/kg/min), oxygen consumption measured on treadmill 13. Wingate Lower Body (Watts/kg), bicycle pedal with fixed resistance for 30 seconds 14. Lateral Bridge R/L (seconds), isometric hold for 30 seconds 15. Lower Y Balance Test R/L (seconds), multi-planar movement to test lower body balance 16. Supine Bridge R/L (seconds), isometric hold until exhaustion 17. Upper Y Balance Test R/L (seconds), multi-planar movement to test upper body balance 18. Diastolic blood pressure (mmHg), average of three readings taken at rest 19. Systolic blood pressure (mmHg), average of three readings taken at rest 20. Maximum heart rate (beats/minute), measured with electronic monitor 21. Resting heart rate (beats/minute, measured with electronic monitor 22. Lean muscle mass (pounds), measured with DEXA overall and segmented body composition Primary cognitive measures, all measured at both pre- and post-intervention (12 weeks): 1. Immediate Free Recall Words (from previously seen words, recall as many as possible)

Secondary

MeasureTime frame
All measured at both pre- and post-intervention (12 weeks): 1. Cortisol (ug/dL) measured using blood test 2. Ferritin (ng/mL) measured using blood test 3. Folate (ng/mL) measured using blood test 4. High-Density Lipoprotein (mg/dL) measured using blood test 5. Low-Density Lipoprotein (mg/dL) measured using blood test 6. Triglycerides (mg/dL) measured using blood test 7. Vitamin B12 (pg/mL) measured using blood test 8 Saturated Fatty Acids (mol %) measured using blood test 9. Monounsaturated Fatty Acids (mol %) measured using blood test 10. Omega-3 PUFAs (mol %) measured using blood test 11. Omega-6 PUFAs (mol %) measured using blood test 12. Trans Fatty Acids (mol %) measured using blood test 13. Lutein density, measured in fovea and parafovea of eye using MPOD device

Countries

United States of America

Contacts

Public ContactAron Barbey
barbey@illinois.edu+1 (0)217 244 2551

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026