Fish Nutrient Supplementation in High-intensity Functional Training

October 3, 2023 updated by: Aristotle University Of Thessaloniki

Effects of a Nutritional Supplement of Proteins, ω3 Fatty Acids and Vitamin D on Physical Performance, Body Composition and Biochemical Profile of Persons Following High-intensity Functional Training

Nowadays, many persons who exercise consume dietary supplements. Previous scientific studies have found that protein supplementation increases muscle mass when combined with an exercise program. In addition, vitamin D probably improves performance and muscle function. Likewise, ω3 fatty acids, apart from improving cardiovascular function, may also increase protein synthesis and performance. Thus, the aim of this study is to investigate the efficacy of a novel aquaculture-based sport supplement of proteins, ω3 fatty acids and vitamin D on physical performance, body composition, and the biochemical profile of persons following high-intensity functional training (HIFT). The efficacy of the experimental supplement (E) will be compared with whey protein (W) and maltodextrin (a carbohydrate) as placebo (P).

Thirty healthy trained individuals (15 male and 15 female), aged 18-35, will take E, W, and P during three 6-week periods of HIFT (a different supplement each period) with three workouts a week and a washout (no supplement) period of 2 weeks between supplementation periods. E is a combination of powder, containing protein and vitamin D, and capsules containing ω3 fatty acids. When on E, participants will receive 0.6 g protein/kg body weight, 20 μg vitamin D, and 1.8 g ω3 fatty acids daily. When on W, they will receive 0.6 g protein/kg body weight and, when on P, they will receive 0.6 g maltodextrin/kg body weight daily. The order of E, W, and P will be random and counterbalanced. Throughout the study, participants will be on isoenergetic nutritional plans to avoid differences in energy intake that might compromise the validity of the study. The dietary plans will be individualized and will provided 1.0 g protein/kg body weight/day.

Participants will undergo measurements of muscle strength, muscle endurance, aerobic capacity, and body composition prior to the first supplementation period, between periods, and after the third period. Also, blood amino acids, fatty acid acids, vitamin D, hematology, biochemistry, and hormones will be measured. To avoid bias, assessors will not know which supplement each participant is taking during each period.

The main hypotheses of the study are: 1) Consumption of E will increase lean body mass compared to W and P; 2) consumption of E will improve muscle strength, muscle endurance, and aerobic capacity compared to W and P; and 3) consumption of E will result in a better blood amino acid, fatty acid, and vitamin D profile.

Study Overview

Study Type

Interventional

Enrollment (Actual)

25

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Thessaloniki, Greece, 57001
        • Laboratory of Evaluation of Human Biological Performance

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Regular training (mixed endurance and resistance training 3-6 times a week, 50 min each session, for the past 4-6 months) as assessed by gym records or questionnaires.
  • Clearance from a pathologist or cardiologist to perform maximal exercise.
  • Mixed isoenergetic diet for the past 4-6 months.

Exclusion Criteria:

  • Smoking (even one cigarette or nicotine-containing device over the past 6 months).
  • Any injuries to the musculoskeletal system that could interfere with the execution of training.
  • Chronic disease.
  • Fish or oyster allergy.
  • Milk allergy.
  • Pregnancy, lactation or planning a pregnancy within the duration of the study.
  • Regular use of prescription medicine or supplements that might affect muscle function or recovery over the past month.
  • Intermittent or religious fasting.
  • Any vegetarian, ketogenic and protein diet.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Fish nutrients - Whey protein - Maltodextrin
Participants will receive fish nutrients, whey protein, and maltodextrin in this order.
Intake of fish protein, omega-3 fatty acids, and vitamin D
Intake of whey protein
Intake of maltodextrin
Other: Fish nutrients - Maltodextrin - Whey protein
Participants will receive fish nutrients, maltodextrin, and whey protein in this order.
Intake of fish protein, omega-3 fatty acids, and vitamin D
Intake of whey protein
Intake of maltodextrin
Other: Whey protein - Fish nutrients - Maltodextrin
Participants will receive whey protein, fish nutrients, and maltodextrin in this order.
Intake of fish protein, omega-3 fatty acids, and vitamin D
Intake of whey protein
Intake of maltodextrin
Other: Whey protein - Maltodextrin - Fish nutrients
Participants will receive whey protein, maltodextrin, and fish nutrients in this order.
Intake of fish protein, omega-3 fatty acids, and vitamin D
Intake of whey protein
Intake of maltodextrin
Other: Maltodextrin - Fish nutrients - Whey protein
Participants will receive maltodextrin, fish nutrients, and whey protein in this order.
Intake of fish protein, omega-3 fatty acids, and vitamin D
Intake of whey protein
Intake of maltodextrin
Other: Maltodextrin - Whey protein - Fish nutrients
Participants will receive maltodextrin, whey protein, and fish nutrients in this order.
Intake of fish protein, omega-3 fatty acids, and vitamin D
Intake of whey protein
Intake of maltodextrin

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Plasma amino acid profile pre-supplementation
Time Frame: Within 2 days before the beginning of supplementation.
Plasma amino acid profile (that is, the concentration of each individual amino acid) will be determined by liquid chromatography - mass spectrometry.
Within 2 days before the beginning of supplementation.
Plasma amino acid profile post-supplementation
Time Frame: Within 2 days after the end of supplementation.
Plasma amino acid profile (that is, the concentration of each individual amino acid) will be determined by liquid chromatography - mass spectrometry.
Within 2 days after the end of supplementation.
Whole-blood fatty acid profile pre-supplementation
Time Frame: Within 2 days before the beginning of supplementation.
Whole-blood fatty acid profile (that is, the concentration of each individual fatty acid) will be determined by gas chromatography.
Within 2 days before the beginning of supplementation.
Whole-blood fatty acid profile post-supplementation
Time Frame: Within 2 days after the end of supplementation.
Whole-blood fatty acid profile (that is, the concentration of each individual fatty acid) will be determined by gas chromatography.
Within 2 days after the end of supplementation.
Maximal dynamic strength of shoulder muscles pre-supplementation
Time Frame: Within 2 weeks before the beginning of supplementation.
Maximal dynamic strength of shoulder muscles will be assessed by measurement of one-repetition maximum.
Within 2 weeks before the beginning of supplementation.
Maximal dynamic strength of shoulder muscles post-supplementation
Time Frame: Within 2 weeks after the end of supplementation.
Maximal dynamic strength of shoulder muscles will be assessed by measurement of one-repetition maximum.
Within 2 weeks after the end of supplementation.
Force-velocity relationship of knee flexors and extensors pre-supplementation
Time Frame: Within 2 weeks before the beginning of supplementation.
Force-velocity relationship of knee flexors and extensors will be assessed in isokinetic dynamometer.
Within 2 weeks before the beginning of supplementation.
Force-velocity relationship of knee flexors and extensors post-supplementation
Time Frame: Within 2 weeks after the end of supplementation.
Force-velocity relationship of knee flexors and extensors will be assessed in isokinetic dynamometer.
Within 2 weeks after the end of supplementation.
Aerobic fitness pre-supplementation
Time Frame: Within 2 weeks before the beginning of supplementation.
Aerobic fitness will be assessed by measurement of maximal oxygen uptake through a maximal graded exercise test on treadmill.
Within 2 weeks before the beginning of supplementation.
Aerobic fitness post-supplementation
Time Frame: Within 2 weeks after the end of supplementation.
Aerobic fitness will be assessed by measurement of maximal oxygen uptake through a maximal graded exercise test on treadmill.
Within 2 weeks after the end of supplementation.
Lean and fat mass pre-supplementation
Time Frame: Within 2 weeks before the beginning of supplementation.
Lean and fat mass of the whole body and its parts (trunk, legs and arms) will be assessed by dual X-ray absorptiometry.
Within 2 weeks before the beginning of supplementation.
Lean and fat mass post-supplementation
Time Frame: Within 2 weeks after the end of supplementation.
Lean and fat mass of the whole body and its parts (trunk, legs and arms) will be assessed by dual X-ray absorptiometry.
Within 2 weeks after the end of supplementation.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Plasma vitamin D concentration pre-supplementation
Time Frame: Within 2 days before the beginning of supplementation.
Vitamin D will be measured by liquid chromatography - mass spectrometry.
Within 2 days before the beginning of supplementation.
Plasma vitamin D concentration post-supplementation
Time Frame: Within 2 days after the end of supplementation.
Vitamin D will be measured by liquid chromatography - mass spectrometry.
Within 2 days after the end of supplementation.
Muscle endurance pre-supplementation
Time Frame: Within 2 weeks before the beginning of supplementation.
Muscle endurance will be assessed by performing multiple sit-ups, knee flexions and knee extensions.
Within 2 weeks before the beginning of supplementation.
Muscle endurance post-supplementation
Time Frame: Within 2 weeks after the end of supplementation.
Muscle endurance will be assessed by performing multiple sit-ups, knee flexions and knee extensions.
Within 2 weeks after the end of supplementation.
Force-velocity relationship of shoulder muscles pre-supplementation
Time Frame: Within 2 weeks before the beginning of supplementation.
Force-velocity relationship of shoulder muscles will be assessed by a linear encoder.
Within 2 weeks before the beginning of supplementation.
Force-velocity relationship of shoulder muscles post-supplementation
Time Frame: Within 2 weeks after the end of supplementation.
Force-velocity relationship of shoulder muscles will be assessed by a linear encoder.
Within 2 weeks after the end of supplementation.
Full blood count pre-supplementation
Time Frame: Within 2 days before the beginning of supplementation.
Full blood count will be performed by flow cytometry.
Within 2 days before the beginning of supplementation.
Full blood count post-supplementation
Time Frame: Within 2 days after the end of supplementation.
Full blood count will be performed by flow cytometry.
Within 2 days after the end of supplementation.
Biochemical analyses pre-supplementation
Time Frame: Within 2 days before the beginning of supplementation.
Plasma glucose, triacylglycerols, total cholesterol, HDL cholesterol, LDL cholesterol, urea, and creatinine (all in mg/dL) will be measured by chemiluminescence in an automated analyzer.
Within 2 days before the beginning of supplementation.
Biochemical analyses post-supplementation
Time Frame: Within 2 days after the end of supplementation.
Plasma glucose, triacylglycerols, total cholesterol, HDL cholesterol, LDL cholesterol, urea, and creatinine (all in mg/dL) will be measured by chemiluminescence in an automated analyzer.
Within 2 days after the end of supplementation.
Plasma enzymes pre-supplementation
Time Frame: Within 2 days before the beginning of supplementation.
Creatine kinase and γ-glutamyltransferase (both in U/L) will be measured by chemiluminescence in an automated analyzer.
Within 2 days before the beginning of supplementation.
Plasma enzymes post-supplementation
Time Frame: Within 2 days after the end of supplementation.
Creatine kinase and γ-glutamyltransferase (both in U/L) will be measured by chemiluminescence in an automated analyzer.
Within 2 days after the end of supplementation.
Hormonal analyses pre-supplementation
Time Frame: Within 2 days before the beginning of supplementation.
Plasma cortisol and testosterone (both in μg/dL) will be measured by immunoluminescence in an automated analyzer.
Within 2 days before the beginning of supplementation.
Hormonal analyses post-supplementation
Time Frame: Within 2 days after the end of supplementation.
Plasma cortisol and testosterone (both in μg/dL) will be measured by immunoluminescence in an automated analyzer.
Within 2 days after the end of supplementation.
Internal load of exercise pre-supplementation
Time Frame: Within the first week of supplementation.
The internal load of exercise will be assessed by telemetric heart rate sensors and software.
Within the first week of supplementation.
Internal load of exercise post-supplementation
Time Frame: Within the last week of supplementation (week 6).
The internal load of exercise will be assessed by telemetric heart rate sensors and software.
Within the last week of supplementation (week 6).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 8, 2021

Primary Completion (Actual)

March 31, 2023

Study Completion (Actual)

September 30, 2023

Study Registration Dates

First Submitted

April 22, 2022

First Submitted That Met QC Criteria

May 31, 2022

First Posted (Actual)

June 2, 2022

Study Record Updates

Last Update Posted (Actual)

October 5, 2023

Last Update Submitted That Met QC Criteria

October 3, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • AQUABIOPRO-FIT1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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