The Effect of Vicia Faba Hydrolysate Supplementation on Muscle Strength Recovery

Description

To investigate the effect of Vicia faba protein concentrate, a protein derived from Fava bean extract, on delayed onset muscle soreness (DOMS). Participants receive either 2.4g/day of PeptiStrong® supplement capsules or placebo capsules for 14 days until a strenuous exercise session. For the last 3 days, 2/3 of them stay on the same treatment and 1/3 of them switch from placebo to PeptiStrong®.

Conditions

Muscle Damage, Muscle

Study Overview

Study Details

Study overview

To investigate the effect of Vicia faba protein concentrate, a protein derived from Fava bean extract, on delayed onset muscle soreness (DOMS). Participants receive either 2.4g/day of PeptiStrong® supplement capsules or placebo capsules for 14 days until a strenuous exercise session. For the last 3 days, 2/3 of them stay on the same treatment and 1/3 of them switch from placebo to PeptiStrong®.

The Effect of Vicia Faba Hydrolysate Supplementation on Muscle Strength Recovery

The Effect of Vicia Faba Hydrolysate Supplementation on Muscle Strength Recovery

Condition
Muscle Damage
Intervention / Treatment

-

Contacts and Locations

Bradenton

Gatorade Sports Science Institute at IMG Academy, Bradenton, Florida, United States, 34210

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Males and females 18 - 45 years of age.
  • * Willing to fast overnight on the 4 testing occasions.
  • * Participants agree to abstain from taking additional supplements throughout the testing period, with particular emphasis placed upon protein-based products (e.g., whey or casein based protein powders; animal derived protein hydrolysates; natural supplements constituted of vegetative protein hydrolysates from rice, fava bean, pea, carrot, spirulina, broccoli, potatoes; marine derived secondary metabolite products or protein hydrolysates including Omega-3 capsules or DHA).
  • * Moderately active (exercise 3-5 days per week)
  • * Fluent in reading, writing, and speaking English
  • * Participants agree to maintain their normal diet and perform only light to moderate exercise for the duration of the study.
  • * BMI between 18.5 and 29.9 kg/m2
  • * Participants agree to refrain from consuming alcohol in the 48 hours leading up to a test day.
  • * Willingness to complete questionnaires, records and diaries associated with the study and to complete all lab visits.
  • * Refrain from any exercise from 48 hours prior to each test or blood draw.
  • * Healthy as determined by General Health Questionnaire.
  • * Non-smoker
  • * Individuals that are glucose-6-phosphate-dehydrogenase deficient. The test product in this study contains fava bean extract which may produce favism in genetically susceptible individuals.
  • * Alcohol or drug abuse in the past year.3. Testosterone or estrogen supplementation (not including women on oral contraceptives)
  • * Pregnant or nursing or planning to become pregnant.
  • * Participation in any other clinical trial in the past 30 days. Participation in any PepsiCo trial in the past 6 months
  • * Volunteers with unstable medical conditions.
  • * Any complaints that could interfere with the ability to exercise.
  • * Individuals who are cognitively impaired or unable to give informed consent.
  • * Any co-morbidities interacting with mobility or muscle metabolism of the lower limbs (e.g. arthritis, spasticity / rigidity, all neurological disorders, paralysis).
  • * Creatine supplements, corticosteroids, NSAIDS, amino acids, injectible peptides, collagen, and nicotinamide (Vit B3/niacin).
  • * Presence or history of neurological disorders or significant psychiatric illness.
  • * Any condition the study investigator believes would interfere with eligibility following the study protocol, effect the study results, or put the subject at undue risk.
  • * Participation in resistance or aerobic exercise within 48 hours of the test days.
  • * Participation of \>3 high-intensity exercise sessions per week.
  • * Undertake recovery methods such as sea swims, foam rolling, cryotherapy or excessive stretching during days 14-17.
  • * Have been in contact with a suspected or confirmed case of COVID-19 in previous 14 days.
  • * Are Hepatitis A- or B-positive or have had a sexual partner infected with hepatitis or HIV and not taking medication.
  • * Are not employed by, or have a parent, guardian, or other immediate family member employed by a company that manufactures any products that compete with any Gatorade product. If you are unsure if a company would be considered a competitor to Gatorade, let the study investigator know the name of the other company and the nature of your relationship to that company before ou sign the informed consent

Ages Eligible for Study

18 Years to 45 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

PepsiCo Global R&D,

Kris Osterberg, PhD, RD, PRINCIPAL_INVESTIGATOR, PepsiCo R&D Life Sciences, Sports Science

Study Record Dates

2025-09-30