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Effects of Collagen Peptide Supplementation on Muscle and Tendon Damage and Function

A Randomized Double-blinded Placebo-controlled Study to Evaluate the Effect of Collagen Peptide (Collagen Peptan) Supplementation on Muscle and Tendon Damage, Repair, and Functional Capacity During Exercise Training Overload

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05425407
Enrollment
22
Registered
2022-06-21
Start date
2021-04-12
Completion date
2021-06-30
Last updated
2022-06-21

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

Conditions

Exercise, Healthy Male Subjects

Keywords

Whey protein, Collagen peptide, Muscle and tendon overload training

Brief summary

The aim of the study is to investigate the acute and short-term effects of collagen peptides (Collagen Peptan) on muscle and connective tissue during an eccentric overload training period. Currently, all studies investigating the effects of post-exercise collagen supplementation did this in the absence of whey proteins, which are part of the standard recommendations for post-exercise recovery. The investigators will therefore investigate whether the combined intake of whey proteins and collagen peptides ensures a better recovery of exercise performance and whether it can prevent or reduce symptoms of muscle and tendon overload during a three-week eccentric overload training period (n = 22).

Interventions

DIETARY_SUPPLEMENTwhey protein

Daily 45g of whey protein supplementation during a three week eccentric training period

DIETARY_SUPPLEMENTwhey protein + collagen peptide

Daily 15g of whey protein and 20g collagen peptide supplementation during a three week eccentric training period

Sponsors

Rousselot BVBA
CollaboratorINDUSTRY
KU Leuven
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Sports participation, including general fitness training, between 2 and 5 hours max per week * Body mass index between 18.5 and 25

Exclusion criteria

* Any kind of injury/pathology that is a contra-indication to perform high-intensity exercise - Intake of any medication or nutritional supplement that could impact muscle protein synthesis and/or exercise performance during the period of the study * Intake of any whey protein, casein of branched-chain amino acid (BCAA) supplements from 1 month prior to the start of the study * Blood donation within 3 months prior to the start of the study * Smoking * Current participation in another research trial * Any other argument to believe that the subject is unlikely to successfully complete the full study

Design outcomes

Primary

MeasureTime frameDescription
Change in countermovement jump performancePretest - 48 hours after the first training session (day 3 of training intervention) - Posttest (day 22 of training intervention)Change in jump height when performing a countermovement jump, measured via a force platform
Change in maximal isometric knee-extension force of the right legPretest - 48 hours after the first training session (day 3 of training intervention) - Posttest (day 22 of training intervention)Change in maximal isometric knee-extension force (angle = 45°) of the right leg
Change in anteroposterior thickness of the right patellar tendonPretest - 48 hours after the first training session (day 3 of training intervention) - Posttest (day 22 of training intervention)Change in anteroposterior thickness of the right patellar tendon
Change in neovascularization of the right patellar tendonPretest - 48 hours after the first training session (day 3 of training intervention) - Posttest (day 22 of training intervention)Neovascularization of the right patellar tendon scored with the Modified Ohberg Score (range 0 - 4; the higher the score, the higher the degree of neovascularization).

Secondary

MeasureTime frameDescription
Change in pain perception at the muscular level (VAS scale)Training 1 (day 1 of training intervention) - Training 2 (day 3 of training intervention) - Training 8 (day 9 of training intervention) - Training 17 (day 19 of training intervention) - Posttest (day 22 of training intervention)Change in pain perception at the muscular level of the right leg, measured via the Visual Analogue Scale (range 0 - 10; the higher the score, the higher the pain level)
Change in the blood concentration of N-terminal propeptide of type I procollagen (P1NP)Pretest - Training 2 (day 3 of training intervention) - Posttest (day 22 of training intervention)Change in blood concentration of N-terminal propeptide of type I procollagen (P1NP; marker of collagen synthesis)
Change in pain perception of the patellar tendon of the right leg (VISA-P)Pretest - Training 1 (day 1 of training intervention) - Training 17 (day 21 of training intervention) - Posttest (day 22 of training intervention)Change in pain perception of the patellar tendon of the right leg, measured via the VISA-P questionnaire (range: 0 - 100; the lower the score, the higher the symptoms of patellar tendon overload)
Change in the blood concentration of creatine kinasePretest - Training 2 (day 3 of training intervention) - Posttest (day 22 of training intervention)Change in blood concentration of creatine kinase (marker of muscle damage)
Change in the blood concentration of Interleukin 6 (IL-6)Pretest - Training 2 (day 3 of training intervention) - Posttest (day 22 of training intervention)Change in blood concentration of Interleukin 6 (IL-6; marker of inflammation)

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026