WheyProtein: The Effects of Whey Protein Supplements on Markers of Exercise-induced Muscle Damage in Resistance-trained Individuals

Sponsor
Indiana University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05100459
Collaborator
(none)
30
1
3
10
3

Study Details

Study Description

Brief Summary

Intense exercise can bring about various side effects to one's body. Less range of motion, increased pain sensitivity, increased muscle swelling, and decreased muscle strength can occur immediately after exercise. These side effects can be referred to exercise induced muscle damage (EIMD) and can sometimes last many days. This study's goal is to evaluate the effects of various protein supplements on EIMD symptoms as well as on blood vessel health during the recovery period after muscle damaging exercise.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Pasture-raised whey protein
  • Dietary Supplement: Conventional whey protein
  • Dietary Supplement: Placebo
N/A

Detailed Description

Eccentric exercise can result in exercise induced muscle damage (EIMD), which can cause an abundance of ultrastructural muscular disruption and pro-inflammatory and pro-oxidant activity in the body, leading to an impairment of muscular force production and range of motion, along with elevated pain sensitivity, increased swelling, and arterial stiffness. Pasture-raised dairy products, obtained from strictly grass-fed cows, have been shown to possess more anti-inflammatory-, antioxidant-, and antihypertensive-like biochemicals compared with conventional products (i.e., with a different nutrient composition from a diet rich in grains versus grasses). However, human research trials on these products, such as whey protein concentrate (WPC), are neglected. This study addresses this gap, with a double-blind, randomized, placebo-controlled trial that compares the effect of conventional WPC versus WPC supplementation reported to be derived from pasture-raised cows on vascular function and indirect markers of muscle damage and inflammation in response to eccentric EIMD in healthy, young, resistance-trained women and men. Thirty resistance-trained individuals will complete an intense EIMD bout consisting of eccentric barbell back squats and then will be assessed 24, 48, and 72 hours post-EIMD for muscle soreness, range of motion, maximal isometric voluntary contraction, peripheral fatigue via magnetic stimulation, countermovement jump, barbell back squat velocity, and vascular function (i.e., arterial stiffness via carotid femoral pulse wave velocity). Subjects will be grouped into a conventional WPC, pasture-raised WPC, and placebo supplementation group and consume their respective supplementation thrice daily immediately post-EIMD until the study's completion.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Basic Science
Official Title:
The Effects of Pasture-raised Versus Conventional Whey Protein Supplementation on Vascular Function and Markers of Exercise-induced Muscle Damage and Inflammation in Resistance-trained Individuals
Anticipated Study Start Date :
Nov 1, 2021
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Pasture-raised whey protein

whey protein from strictly grass fed cows

Dietary Supplement: Pasture-raised whey protein
25 grams of protein delivered 3 times daily
Other Names:
  • Premium Blend Protein, Pasture Raised, Grass Fed, unflavored, Muscle Feast, Nashport, OH, USA
  • Experimental: Conventional whey protein

    whey protein from conventional animal feeding operation

    Dietary Supplement: Conventional whey protein
    25 grams of protein delivered 3 times daily
    Other Names:
  • 100% Whey Protein Powder, unflavored, TGS Nutrition, Las Vegas, NV, USA
  • Placebo Comparator: Placebo

    Maltodextrin given in iso-caloric amounts to protein

    Dietary Supplement: Placebo
    Iso-caloric placebo taken 3 times daily like the protein supplementation
    Other Names:
  • Maltodextrin, Bulk Supplements, Henderson, NV, USA
  • Outcome Measures

    Primary Outcome Measures

    1. Titin [Four days]

      Muscle damage assessment via urinary titin via ELISA (MBS2881644, Human Titin ELISA® Kit, MyBioSource.com, Inc., San Diego, USA). Units: pmol

    2. Isometric torque [Four days]

      Isometric torque assessment of right leg extensors will be conducted at a knee angle of 90 degrees using a calibrated load cell (model Z Tension Load Cell; Dillon, Fairmont, MN) Units: Nm

    3. Range of motion [Four days]

      Hamstring flexibility and stiffness will be measured using a sit-and-reach box (Lafayette Instrument Company, Lafayette, IN) test. Units: cm

    4. delayed onset muscle soreness [Four days]

      Visual analog scale of muscle soreness (delayed onset muscle soreness; DOMS) - Knee extensor soreness will be assessed using a visual analogue scale with "no soreness" indicated at one end (score 0) and "unbearably painful" at the other (score 100). Units: arbitrary units

    5. Pain pressure threshold [Four days]

      Muscle tenderness, known as pain pressure threshold, will be quantified using a digital algometer (Force One, Wagner Instruments, Greenwich, CT) on pre-marked sites at two specific points on the quadriceps (rectus femoris-RF and vastus lateralis-VL) and one on the calf (gastrocnemius-GM). Units: percentage change from baseline

    6. Peripheral Fatigue [Four days]

      Peripheral fatigue will be assessed via magnetic stimulation (Magstim 200-2; Jali Medical, Newton, MA, USA) of the femoral nerve, which will be used to elicit a quadriceps twitch. Units: Nm

    7. Countermovement Jump [Four days]

      A linear position transducer (GymAware Powertool; Kinetic Performance Technology, Canberra, Australia) interfaced with an iPad (Apple, CA, USA) will be used to calculate countermovement jump (CMJ) height. Units: cm

    8. Barbell back squat velocity [Four days]

      The mean velocity of the barbell will be measured using the linear position transducer as per the load velocity profile relationship. Units: m/s

    Secondary Outcome Measures

    1. Arterial Stiffness [Four days]

      Utilizing carotid femoral pulse wave velocity via applanation tonometry, considered the non-invasive gold standard of central arterial stiffness, the ATCOR SphygmoCor® (Naperville, IL, USA) device will be utilized. Units: m/sec

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 40 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Men and women 18-40 years old

    • ≥3 months uninterrupted training of ≥3 days/week of resistance training

    • Self-reported to be healthy

    Exclusion Criteria:
    • Not within defined age range

    • History of allergy to dairy products

    • History of experiencing pain while exercising in the lower extremities (i.e., hips/knees)

    • Current use of anti-inflammatory/anti-pain medication (i.e., nonsteroidal anti-inflammatory drugs (NSAIDs) such as Tylenol, Advil, or Aleve

    • Are pregnant or could possibly be pregnant by self-report

    • People who answer 'yes' to any of the pre-participation screening questions on the PAR-Q questionnaire.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Indiana University School of Public Health Bloomington Indiana United States 47405

    Sponsors and Collaborators

    • Indiana University

    Investigators

    • Principal Investigator: Timothy D Mickleborough, Ph.D., Indiana University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Tim Mickleborough, Professor, Indiana University
    ClinicalTrials.gov Identifier:
    NCT05100459
    Other Study ID Numbers:
    • 12559
    First Posted:
    Oct 29, 2021
    Last Update Posted:
    Oct 29, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 29, 2021