AzTrials
AzTrials

Healthy SubjectsNCT07420933

Pea vs Whey Protein Supplementation With Resistance Training on Young Adults' Strength, Body Composition, and Metabolic Parameters

A study testing Protein Isolate and Progressive Resistance Exercise Training (PRE) in people with Healthy Subjects, run by Texas Woman's University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The goal of this clinical trial is to compare the impact of pea protein or whey protein supplementation during a progressive resistance exercise (PRE) regimen on body composition and strength in young adults who are not undergoing regular strength training. The main questions it aims to answer are: 1. Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Healthy Subjects
What is being tested?
Protein Isolate and Progressive Resistance Exercise Training (PRE)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
34 participants
Where
1 siteUnited States
Study dates
3 Feb 2024to 6 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Healthy Adults 18-30y
  • BMI between 18.5 - 28 kg/m**2
  • The subjects will be excluded if:
  • they have a history or current diagnosis of cardiovascular disease, cancer, diabetes, gastrointestinal disorders, or metabolic disorders.
  • they use tobacco products
  • consume alcohol as defined as >2 drinks per day,
Show all 11Show fewer
  • follow a special diet
  • reported recent significant body weight changes (>5% prior 3 months)
  • report an intolerance or allergy to ingredients in the supplements.
  • report regular consumption of other muscle or metabolic stimulating products or drugs such as creatine, other amino acids or protein supplements, growth hormone or derivatives, or ergogenic aids including steroids.
  • if they answer "no" to any question on the Physical Activity Readiness Questionnaire which would indicate that the subject cannot safely participate in an exercise program.

Who cannot join

None listed.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Texas Woman's University Institute of Health Sciences Houston Center

    Houston, Texas, 77008

Other trials in United States

About this study

Official title: The Effect of Pea Protein Supplementation on Muscle Hypertrophy and Metabolic Parameters in Young Adults Following an 8-week Resistance Training Program

The goal of this clinical trial is to compare the impact of pea protein or whey protein supplementation during a progressive resistance exercise (PRE) regimen on body composition and strength in young adults who are not undergoing regular strength training. The main questions it aims to answer are:

  1. Do lean body mass changes differ between supplement groups following a progressive resistance exercise PRE training program?
  2. Does improvements in muscle strength differ between groups following a PRE training program?
  3. Does glucose, insulin, and essential amino acid appearance and clearance rate differ between groups following a PRE training program? Researchers will compare pea protein supplementation to whey protein supplementation to see if there are any differences in body composition and strength
Read more

Participants will:

  • Consume Pea or Whey protein supplement twice daily for 8 weeks
  • Participate in a PRE training program twice weekly for approximately 1.5 hours per day
Read the detailed description

Adequate dietary protein intake is essential for maximizing skeletal muscle hypertrophy and strength gains during progressive resistance exercise (PRE) training. Whey protein isolate is commonly used to support these adaptations; however, there is limited clinical evidence comparing plant-based protein supplements with whey protein when protein dose is controlled and combined with structured resistance training. Pea protein isolate represents a sustainable, plant-based alternative, but its effectiveness in promoting muscle accretion, strength, and metabolic responses relative to whey protein isolate has not been fully characterized. Therefore, this study will compare the effects of pea protein isolate and whey protein isolate supplementation on changes in lean body mass, muscle strength, and postprandial metabolic responses in healthy, untrained young adult males. Participants will be randomized in a double-blind, parallel-group design to consume either pea protein isolate or whey protein isolate for 8 weeks while completing a supervised, PRE training program. Lean body mass and strength outcomes will be assessed before and after the intervention, and acute postprandial essential amino acid, glucose, and insulin responses will be evaluated following standardized protein ingestion at baseline and post-intervention.

Being tested
Protein Isolate, Progressive Resistance Exercise Training (PRE)
Keywords
pea protein isolate, whey protein isolate, progressive resistance exercise, body composition, strength, essential amino acid

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Protein IsolateDietary supplement

    Participants in this arm will consume protein isolate (24g/sachet) twice daily for 8 weeks.

  • Progressive Resistance Exercise Training (PRE)Behavioural

    Based on the resistance training guidelines from the American College of Sports Medicine, each subject will attend two supervised resistance training sessions weekly for a duration of 8 weeks. A minimum two day rest between PRE sessions will be required. Twelve exercises that targets each major muscle group will be conducted at each exercise session in the order listed below:

    1. Seated chest press
    2. Lat pulldown
    3. Military Press
    4. Seated row
    5. Bicep Curl
    6. Triceps Extension
    7. Leg Press
    8. Leg extension
    9. Leg Curl
    10. Heel Raise
    11. Abdominal curls
    12. Back extension At the first exercise session, each subject's 1-RM will be estimated for the exercises listed above
Study groups in NCT07420933
Study groupRoleWhat they receive
Pea ProteinExperimentalParticipants in this arm will consume pea protein isolate (24g/sachet) twice daily for 8 weeks while participating in an 8-week PRE program (2, 1.5hr sessions per week)
Receives: Dietary Supplement: Protein Isolate; Behavioral: Progressive Resistance Exercise Training (PRE)
Whey ProteinActive comparatorParticipants in this arm will consume whey protein isolate (24g/sachet) twice daily for 8 weeks while participating in an 8-week PRE program (2, 1.5hr sessions per week)
Receives: Dietary Supplement: Protein Isolate; Behavioral: Progressive Resistance Exercise Training (PRE)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Difference in body composition

    Differences in lean mass (kg, kg/m^2, and % total mass) and fat mass (kg, and % total mass) assessed using Dual Energy X-ray Absorptiometry (DXA; Horizon W, Hologic, Marlborough, MA)

    Measured: Baseline and 8 weeks

  2. Difference in muscle strength

    Differences in muscle strength assessed by maximal isometric force produced by quadriceps (Nm) using a Biodex System 3 dynamometer, hand grip (kg) using a handgrip dynamometer, 1-Rep Max for chest press (kg), and 1-Rep Max for leg press (kg)

    Measured: Baseline and 8 weeks

Secondary outcomes (1)
  1. Nutritional Metabolic Biomarkers

    Differences in essential amino acid (Histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine) cMax and iAUC, glucose (cMax and iAUC), and insulin (cMax and iAUC) will be measured from plasma following a protein load (0.3 g/kg body weight of pea- or whey-protein isolate)

    Measured: Baseline and 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Feb 2026
  2. Study start3 Feb 2024
  3. Primary completion6 Dec 2025
  4. Study completion6 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
34 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07420933
Sponsor's protocol ID
PProtRCT-FY2019-182
Status last verified
Dec 2025
First submitted
19 Dec 2025
Last updated
19 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Protein Isolate and Progressive Resistance Exercise Training (PRE) in people with Healthy Subjects, run by Texas Woman's University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 11 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Difference in body composition (time frame: Baseline and 8 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Feb 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in