Exercise Clinical Trial
Official title:
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
NCT number | NCT05425407 |
Other study ID # | S64402 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 12, 2021 |
Est. completion date | June 30, 2021 |
Verified date | June 2022 |
Source | KU Leuven |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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).
Status | Completed |
Enrollment | 22 |
Est. completion date | June 30, 2021 |
Est. primary completion date | May 30, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 30 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
Belgium | Exercise Physiology Research Group | Leuven | Vlaams-Brabant |
Lead Sponsor | Collaborator |
---|---|
KU Leuven | Rousselot BVBA |
Belgium,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in countermovement jump performance | Change in jump height when performing a countermovement jump, measured via a force platform | Pretest - 48 hours after the first training session (day 3 of training intervention) - Posttest (day 22 of training intervention) | |
Primary | Change in maximal isometric knee-extension force of the right leg | Change in maximal isometric knee-extension force (angle = 45°) of the right leg | Pretest - 48 hours after the first training session (day 3 of training intervention) - Posttest (day 22 of training intervention) | |
Primary | Change in anteroposterior thickness of the right patellar tendon | Change in anteroposterior thickness of the right patellar tendon | Pretest - 48 hours after the first training session (day 3 of training intervention) - Posttest (day 22 of training intervention) | |
Primary | Change in neovascularization of the right patellar tendon | 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). | Pretest - 48 hours after the first training session (day 3 of training intervention) - Posttest (day 22 of training intervention) | |
Secondary | Change in pain perception at the muscular level (VAS scale) | 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) | 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) | |
Secondary | Change in pain perception of the patellar tendon of the right leg (VISA-P) | 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) | Pretest - Training 1 (day 1 of training intervention) - Training 17 (day 21 of training intervention) - Posttest (day 22 of training intervention) | |
Secondary | Change in the blood concentration of creatine kinase | Change in blood concentration of creatine kinase (marker of muscle damage) | Pretest - Training 2 (day 3 of training intervention) - Posttest (day 22 of training intervention) | |
Secondary | Change in the blood concentration of Interleukin 6 (IL-6) | Change in blood concentration of Interleukin 6 (IL-6; marker of inflammation) | Pretest - Training 2 (day 3 of training intervention) - Posttest (day 22 of training intervention) | |
Secondary | Change in the blood concentration of N-terminal propeptide of type I procollagen (P1NP) | Change in blood concentration of N-terminal propeptide of type I procollagen (P1NP; marker of collagen synthesis) | Pretest - Training 2 (day 3 of training intervention) - Posttest (day 22 of training intervention) |
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