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CompletedNCT07119749Updated Aug 13, 2025

Vegan Whey Protein for Muscle Anabolism and Post-exercise Recovery

An interventional study of Stable isotope tracer consumption and DXA scan in Muscle Soreness, sponsored by University of Birmingham. Completed at 1 site in United Kingdom. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-08-13.

Sponsored by University of Birmingham · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 1 year 8 months after the study started (first participant enrolled Sep 2023, registered May 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
27
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

This study will be a randomised, double-blind trial where participants will be randomly assigned to consume either a i) vegan whey protein; ii) a whey protein; or iii) a non-protein carbohydrate control supplement for 3 days following strenuous eccentric knee extension exercise. For the duration of the study period, participants will orally consume deuterated water stable isotope tracer (D2O). This, together with repeated blood sampling and muscle biopsies will allow for the calculation of free-living myofibrillar protein synthesis rates under conditions of rest and over 24-, 48- and 72-hours post-exercise recovery.

Read the detailed description

Participants will be asked to attend 7 experimental visits at the School of Sport, Exercise and Rehabilitation Sciences at the University of Birmingham. The first of the 7 visits will be to assess participant eligibility and to gain written informed consent, where the remaining 6 visits will involve experimental procedures. Briefly, participants will be randomly assigned to ingest one of three nutritional supplements (i: vegan whey protein isolate; ii: whey protein isolate; iii: a non-protein carbohydrate control), 3 times a day for a total of 3 days following an acute bout of unilateral lower-limb eccentric exercise. The study will be run in a double-blinded fashion, where the researchers and participants will both be unaware of nutritional treatment allocation. The amount of protein in each supplemental beverage is prescribed based on total body mass (0.3 g of protein per kg of body mass). As well, for 3 days before and 3 days after the exercise bout, participants will be provided with a standardised diet to consume. For the 3 days before the exercise bout, all participants will consume an identical diet, with a protein intake of 1 g per kg body mass and diets will be energy-matched between treatment groups. For the subsequent 3 days, participants assigned to each of the protein supplementation groups (whey protein or vegan whey protein) will have a daily protein intake of 1.9 g per kg body mass, whereas participants assigned to the carbohydrate control group will maintain protein intake at 1 g per kg body mass. Measures of muscle function, soreness and thickness will be taken before and at various time points after the eccentric exercise, details of which can be found below. To assess the muscle protein synthetic response to each nutritional treatment, participants will orally consume a stable isotope tracer ("heavy water") for a period of 9 days, and muscle biopsies and saliva samples will be taken periodically. An outline of each experimental visit is outlined below.

02

Conditions studied

  • Muscle Soreness

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03

In context

Myalgia

282 studies on the registry are indexed under Myalgia; 43 are open to participants now.

This study's enrollment of 27 is below the median of 44 across 241 interventional studies indexed under Myalgia.

Browse Myalgia studies →

Lead sponsor

University of Birmingham is the lead sponsor of 179 studies on the registry; 30 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Males, and females aged 18-40 years with a body mass index between 18.5 and 29.9 kg/m2
  • Healthy individuals free from metabolic and respiratory disease
  • Recreationally active or trained (complete at least 150 mins of moderate physical activity, or 75 mins of vigorous physical activity per week, identify with a certain sport, intend to compete in local competition)
  • Understands and is willing, able and likely to comply with all study procedures and restrictions
  • Demonstrates an understanding of the study and willingness to participate, as evidenced by voluntary written informed consent

Exclusion criteria

Exclusion Criteria:

  • Aged \<18 or >40 years
  • Pregnancy and Breastfeeding
  • Body mass index \<18.5 or >29.9 kg/m2
  • Regular participation (i.e., >3 times weekly for the previous 3 months) in structured exercise or sport with a large eccentric component, such as trail running, soccer, basketball etc.
  • Elite athletes or sports-people who compete nationally or internationally
  • Habitual smokers
  • History of respiratory or metabolic disease
  • Any allergies or intolerances to the study materials, protein supplements and food ingredients to be used in this study. In particular, those with an allergy to lidocaine and lactose will be excluded
  • Use of any medication or supplements known to affect muscle protein metabolism (e.g., beta-blockers, corticosteroids, analgesics, or non-steroidal anti-inflammatories). Additional medications and/or supplementation aids (e.g., vitamins) will be deemed inappropriate based on the PI's discretion
  • Any current or history of musculoskeletal injury
  • Any history of medical or surgical events that may affect the study outcomes
  • Previous participation in a research-based exercise protocol designed to induce severe muscle damage in the last 6 months
  • Habitual protein intakes \<0.8 g/kg body mass/day or > 2.2 g/kg body mass/day
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
27 participants (actual)

Study arms

  • Experimental
    Vegan whey protein

    3 x daily supplementation of 0.3 g per kg body mass of vegan whey protein isolate for 3 days following an acute bout of lower-body unilateral resistance exercise

    Other: Stable isotope tracer consumption · Radiation: DXA scan · Behavioral: Controlled diet · Other: Saliva sample · Other: Blood sample · Procedure: Muscle biopsy · Behavioral: Resistance exercise · Other: Isometric strength test · Dietary Supplement: Supplement

  • Active comparator
    Dairy whey protein

    3 x daily supplementation of 0.3 g per kg body mass of dairy whey protein isolate for 3 days following an acute bout of lower-body unilateral resistance exercise

    Other: Stable isotope tracer consumption · Radiation: DXA scan · Behavioral: Controlled diet · Other: Saliva sample · Other: Blood sample · Procedure: Muscle biopsy · Behavioral: Resistance exercise · Other: Isometric strength test · Dietary Supplement: Supplement

  • Placebo comparator
    Carbohydrate placebo

    3 x daily supplementation of isocaloric carbohydrate placebo for 3 days following an acute bout of lower-body unilateral resistance exercise

    Other: Stable isotope tracer consumption · Radiation: DXA scan · Behavioral: Controlled diet · Other: Saliva sample · Other: Blood sample · Procedure: Muscle biopsy · Behavioral: Resistance exercise · Other: Isometric strength test · Dietary Supplement: Supplement

Interventions

  • OtherStable isotope tracer consumption

    Daily consumption of oral deuterium oxide (0.3 ml per kg of lean body mass) to equilibrate in body water and become slowly incorporated into muscle protein, enabling measurement of muscle protein synthesis rates

  • RadiationDXA scan

    Whole body DXA scan to assess lean body mass for prescription of deuterium oxide tracer

  • BehavioralControlled diet

    Participant will be asked to consume a provided 6-day diet package that will be prepared by the research team. This package will include 3 meals per day plus snacks

  • OtherSaliva sample

    Obtained from participants by asking them to spit into a tube each day during the study, for 11 days in total.

  • OtherBlood sample

    Resting venous blood sample from a forearm vein on 6 separate occasions

  • ProcedureMuscle biopsy

    A highly experienced researcher will sample a small section of muscle (\~200 mg) from the vastus lateralis muscle under local anaesthetic (5 ml, 1% Lidocaine)

  • BehavioralResistance exercise

    participants will complete 8 sets of 10 repetitions of unilateral eccentric knee extensions on an isokinetic dynamometer.

  • OtherIsometric strength test

    Bilateral isometric strength will be measured using a well-established protocol on an isokinetic dynamometer.

  • Dietary supplementSupplement

    Consumption of 3 supplements a day for 3 days following resistance exercise. All supplements are commercially available.

06

What researchers measure

Primary outcomes

  1. Myofibrillar protein synthesis rates (iMyoPS)

    1\. Changes in myofibrillar protein synthesis rates of the exercised leg, both over time (1, 24, 48 and 72 hours) during post-exercise recovery and between supplemental groups (vegan whey, whey protein, and non-protein carbohydrate control). Determined by assessing the incorporation of deuterium in muscle, relative to saliva and blood deuterium enrichment.

    Time frame: 3 days pre-exercise and 3 days post-exercise

  2. Muscle function

    4\. Changes in leg muscle architecture followed by leg strength and neural activation will be assessed pre- and at 1, 8-, 24-, 48- and 72-hours post-exercise. Muscle architecture will be assessed using ultrasound and specifically, shear-wave elastography. Change in isometric strength will be assessed on a Biodex dynamometer at a set knee angle while simultaneously assessing neural activation. Participants will be asked to perform a maximal voluntary contraction (MVC) for 5 seconds while neural activation is measured using the interpolated twitch method. There will be 3 measurements for MVC and neural activation with 2 minutes rest between each attempt on visit

    Time frame: pre- and 1, 4, 24, 48 and 72 hr post-exercise

  3. Intramuscular anabolic signalling

    2\. Changes in the total protein content and phosphorylation status of key anabolic signalling proteins, both over time post-exercise and between the supplemental groups. Assessed by Western Blotting of muscle biopsy samples

    Time frame: pre- and 1-hr and 24-hr post-exercise

  4. Muscle morphology

    3\. Changes in muscle structure and morphology at pre- and at 1, 24-, 48- and 72-hours post-exercise will be assessed via immunofluorescence microscopy of muscle biopsy samples.

    Time frame: pre- and 1, 24, 48 and 72 hr post-exercise

Secondary outcomes

  1. Muscle soreness

    Subjective ratings of muscle soreness will be measured via completion of validated visual analogue scales (no muscle soreness 0 - worst imaginable muscle soreness 100 mm)

    Time frame: pre- and 1, 4, 24, 48 and 72 hr post-exercise

  2. Blood markers of muscle damage

    Plasma concentrations of systemic markers of muscle damage (creatine kinase, lactate dehydrogenase etc) will be measured from blood samples

    Time frame: pre- and 1, 4, 24, 48 and 72 hr post-exercise

07

Study locations

1 site
  • School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham
    Birmingham, West Midlands B15 2TT, United Kingdom
08

References and documents

Publications

  • Rogers LM, Korzepa M, Belfield AE, Quinlan JI, Wallis GA, Breen L. Muscle Recovery and Myofibrillar Protein Synthesis after Damaging Exercise with Recombinant Bovine beta-Lactoglobulin, Dairy-Derived Whey or Carbohydrate Supplementation in Young Healthy Adults. J Nutr. 2026 May;156(5):101321. doi: 10.1016/j.tjnut.2025.101321. Epub 2026 Jan 5. PubMed 41500363 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 13, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07119749
Lead sponsor
University of Birmingham
Responsible party
Sponsor
First posted
Aug 13, 2025
Start date
Sep 1, 2023
Primary completion
Nov 22, 2024
Completion
Nov 22, 2024
Last update
Aug 13, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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