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Protein Supplements to Cyclists

Effekt of Marine Peptide Supplementation on Recovery Following Endurance Cycling

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03136133
Enrollment
16
Registered
2017-05-02
Start date
2017-09-14
Completion date
2018-12-31
Last updated
2017-09-15

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

Conditions

Reconstitution After Bicycle Intervention

Brief summary

To investigate the effect of marine peptide combined with dietary protein on the capacity to recover after exhaustive endurance cycling as measured by exercise capacity and blood glucose homeostasis.

Detailed description

The current study uses cyclists as test subjects since they represent a physical demanding sport requiring both high endurance capacity and muscle strength. In the recovery phase following exhaustive physical activity there is a need both for rebuilding the muscle energy stores, for muscle repair and for compensatory muscle cell development. Therefore, marine peptide combined with dietary protein will be given in order to examine the capacity to recover after exhaustive endurance cycling.

Interventions

DIETARY_SUPPLEMENTActive protein drink

Fish protein from cod to be used for man after Heavy excercise to restitute

Sponsors

Firmenich Bjørge Biomarine As
CollaboratorUNKNOWN
Haukeland University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Protein drink With matching placebo

Intervention model description

Crossover, placebo controlled

Eligibility

Sex/Gender
MALE
Age
40 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Signed informed Consent * The subject is a man between 40-50 years * The subject has a body mass index (BMI) between 19-29 * Willing to comply with all study procedures and be available for the length of the study * In good general health as judged by the physician at the screening visit

Exclusion criteria

* The subject has had surgery or trauma with significant blood loss or has donated blood within the last 3 months prior to the screening visit * Diabetes type 1 or 2, or persistent high blood sugar levels * The subject has tested positive for human immunodeficiency virus (HIV) * Hepatitis B surface antigen (HBsAg), or hepatitis C virus antibody (anti-HCV) * The subject has taken any investigational drugs within 1 month prior to screening * Treated with antibiotics within 3 months prior to screening (oral, parenteral or rectal), but not spray or ointment * Treated with steroids within 1 month prior to screening (including oral treatment) * Treated with medication that effects the intestinal function such as, H2- protonpump inhibitors, diuretics, antiemetics, antidepressants, antacids,

Design outcomes

Primary

MeasureTime frame
Change in blood glucose compared to placeboChange from baseline to every 30 minutes after dosing, for 2 hours

Secondary

MeasureTime frame
Change in insulin-like peptide 5 compared to placeboChange from baseline to every 30 minutes after dosing, for 2 hours

Countries

Norway

Contacts

Primary ContactTrygve Hausken, MD
trygve.hausken@helse-bergen.no+4755972134
Backup ContactBente Frisk
bente.frisk@helse-bergen.no+4755970440

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026