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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03665948
Other study ID # ULS00004
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 9, 2017
Est. completion date December 20, 2024

Study information

Verified date May 2024
Source Poznan University of Physical Education
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the presented study was to assess the influence of Ketogenic (KD) and a carbohydrate diet with a low glycemic index (CHO-LGI) of a 4-week diet on physical and specific performance capacity, exercise metabolism, as well as concentrations of the selected biochemical blood markers in Crossfit- trained athletes, in a randomised and parallel trial.


Description:

The impact of various dietary strategies, including the alternative ketogenic diet - recently popular among strength athletes, has not been unequivocally assessed in the high-intensity sport disciplines that Crossfit belongs to. There is also a lack of data in these disciplines about the potential longer adaptation of athletes to the very low carbohydrate intake resulting from the ketogenic diet and its impact in high-intensity Crossfit training. Therefore, the purpose of this study was the assessment of the influence of a 4-week KD and a CHO-LGI diet on physical and specific performance capacity, exercise metabolism, as well as concentrations of the selected biochemical blood markers in Crossfit- trained athletes, in a randomised and parallel trial.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 70
Est. completion date December 20, 2024
Est. primary completion date November 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - written consent to participate, - a current medical clearance to practice sports, - training experience: at least 2 years, - minimum of 4 workout sessions (Crossfit) a week. Exclusion Criteria: - current injury, - any health-related contraindication, - declared general feeling of being unwell, - unwilling to follow the study protocol, - smoking, illicit drug use, alcohol consumption greater than 1-2 drinks/week, dietary supplements use less than 3 weeks before the study, - females- being pregnant or planning to become pregnant during the study.

Study Design


Intervention

Other:
Dietary Intervention - Ketogenic Diet (KD)
The experimental procedure for each randomly assigned participant included a 4-week of KD diet.
Dietary Intervention - Low-Glycemic Index Diet (CHO-LGI)
The experimental procedure for each randomly assigned participant included a 4-week of CHO-LGI diet.

Locations

Country Name City State
Poland Institute of Human Nutrition and Dietetics, Poznan University of Life Sciences Poznan

Sponsors (3)

Lead Sponsor Collaborator
Poznan University of Physical Education Poznan University of Life Sciences, Poznan University of PhysED

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in aerobic capacity following dietary intervention Baseline and after 4 weeks
Primary Changes in CrossFit-specific performance capacity (Fight Gone Bad test) following dietary intervention The number of correctly performed repetitions of exercises (reps) Baseline and after 4 weeks
Primary Changes in energy substrates utilization following dietary intervention Fats (g/min) and carbohydrates (g/min) oxidation analysis Baseline and after 4 weeks
Secondary Changes in fat mass and fat free mass following dietary intervention Fat mass (kg) and fat free mass (kg) analysis Baseline and after 4 weeks
Secondary Changes of red and white blood cell concentration in blood following dietary intervention Red blood cells (RBC) [mln/mm³] and white blood cells (WBC) [mln/mm³] concentration analysis Baseline and after 4 weeks
Secondary Changes in blood glucose and hemoglobin concentration following dietary intervention Hemoglobin (Hb) [g/dl] and glucose [g/dl] concentration analysis Baseline and after 4 weeks
Secondary Changes in blood hematocrit levels following dietary intervention Hematocrit (HCT) [%] level analysis Baseline and after 4 weeks
Secondary Changes of testosterone, cortisol, urea, lactate and pyruvate concentration in blood following dietary intervention Testosterone [mmol/L], cortisol [mmol/L], urea [mmol/L], lactate [mmol/L] and pyruvate [mmol/L] concentration analysis Baseline and after 4 weeks
Secondary Changes of creatine kinase, lactate dehydrogenase, alanine aminotransferase and aspartate aminotransferase activity in blood after following dietary intervention Creatine kinase [U/L], lactate dehydrogenase [U/L], alanine aminotransferase [U/L] and aspartate aminotransferase [U/L] activity analysis Baseline and after 4 weeks
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