Protein Supplements to Cyclists

NCT ID: NCT03136133

Last Updated: 2017-09-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-09-14

Study Completion Date

2018-12-31

Brief Summary

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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

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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.

Conditions

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Reconstitution After Bicycle Intervention

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Crossover, placebo controlled
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
Protein drink With matching placebo

Study Groups

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Active protein drink

Active protein drink

Group Type ACTIVE_COMPARATOR

Active protein drink

Intervention Type DIETARY_SUPPLEMENT

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

Placebo drink

Placebo drink

Group Type PLACEBO_COMPARATOR

Active protein drink

Intervention Type DIETARY_SUPPLEMENT

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

Interventions

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Active protein drink

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

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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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,
Minimum Eligible Age

40 Years

Maximum Eligible Age

50 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Firmenich Bjørge Biomarine As

UNKNOWN

Sponsor Role collaborator

Haukeland University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Haukeland University Hospital

Bergen, , Norway

Site Status RECRUITING

Countries

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Norway

Central Contacts

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Trygve Hausken, MD

Role: CONTACT

+4755972134

Bente Frisk

Role: CONTACT

+4755970440

Facility Contacts

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Trygve Hausken, MD

Role: primary

References

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Mjos I, Thorsen E, Hausken T, Lied E, Nilsen RM, Bronstad I, Edvardsen E, Frisk B. The effect of low dose marine protein hydrolysates on short-term recovery after high intensity performance cycling: a double-blinded crossover study. J Int Soc Sports Nutr. 2019 Oct 29;16(1):48. doi: 10.1186/s12970-019-0318-3.

Reference Type DERIVED
PMID: 31665070 (View on PubMed)

Other Identifiers

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2017/56

Identifier Type: -

Identifier Source: org_study_id