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临床试验/NCT05697900
NCT05697900已完成不适用

Creatine Monohydrate Versus Creatine Hydrochloride on Strength and Body Composition in Elite Team-Sport Athletes: A Three-arm Placebo-controlled Randomized Clinical Trial

Dynamical Business and Science Society - DBSS International SAS2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2021年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
48
试验地点
2
主要终点
Neuromuscular strength

研究概览

简要总结

A triple-arm double-blinded placebo-controlled repeated-measures randomized clinical trial in Colombian elite team-sport athletes. The aim is to evaluate the effects on strength-related parameters and body composition after eight weeks of supplementation with creatine monohydrate (CrM) and creatine hydrochloride (Cr-HCl). The study will be reported following the Consolidated Standards of Reporting Trials (CONSORT) extension to Multi-Arm Parallel-Group Randomized Trials. All variables will be measured at baseline and after eight weeks.

详细描述

Creatine monohydrate (CrM) is the most studied nutritional supplement and, therefore, one of the most popular ergogenic nutritional aids for athletes. Studies have shown that CrM supplementation increases intramuscular creatine concentrations which enhances exercise performance and improves body composition in different populations (from young athletes to older adults).

It is important to note that the U.S. Food and Drug Administration (FDA) have recognized CrM as a safe ingredient (Generally Recognized as Safe, GRAS - No. GRN 000931). In spite of this, other forms such as creatine chloride (Cr-HCl) have been marketed as a more bioavailable sources of creatine. Since there are not studies that rigorously compare the effects of CrM versus Cr-HCl on physical performance and body composition, the aim of this study is to evaluate the effects of a 8-week supplementation protocol with the two forms of creatine (comparing to placebo) on neuromuscular strength and body composition in Colombian elite team-sport athletes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

盲法说明

This was a double-blinded clinical trial since participants and those assessing the outcomes were blinded to the intervention. All groups were given small metallic plastic bags with five grams of powder identical in size, shape, and color but the placebo contained maltodextrin (Tecnas S.A., Medellín, Colombia).

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Practicing team sports at the competitive level (handball and softball)
  • Having at least one year of competitive sports training experience (including strength training at least three times a week),
  • Being attended at INDEPORTES Antioquia.

排除标准

  • Those who do not wish to participate voluntarily (do not sign informed consent),
  • Those who were taking nutritional supplements (including creatine) eight weeks prior to the start of the study,
  • Those who had a diagnosed pathology or health issues.

结局指标

主要结局

Neuromuscular strength

时间窗: Eight weeks

The load-velocity profile in squat and bench press exercises will be obtained with a linear position transducer (load in kilograms versus mean propulsive velocity in meters per second).

Upper-limb muscle strength

时间窗: Eight weeks

Maximal shoulder external and internal strength will be measure with a isokinetic dynamometer.

Lower-limb muscle power

时间窗: Eight weeks

Countermovement and drop jump will be performed on contact mat (height in centimeters and time of flight in seconds)

次要结局

  • Body composition(Eight weeks)

研究者

发起方
Dynamical Business and Science Society - DBSS International SAS
申办方类型
Network
责任方
Sponsor

研究点 (2)

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