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临床试验/NCT05339308
NCT05339308已完成不适用

Effects of Magnesium Oil Application on the Muscle Contractile Properties

University of Ljubljana2 个研究点 分布在 2 个国家目标入组 18 人开始时间: 2022年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
2
主要终点
Skeletal Muscle Contractile Properties

研究概览

简要总结

This study will aim to investigate the effects of magnesium oil administration on skeletal muscle contractile properties.

详细描述

Aim: This study will aim to investigate the effects of magnesium oil administration on skeletal muscle contractile properties (SMcp).

Design: Randomized controlled study

Participants: For this purpose, investigators will recruit 40 recreationally active and healthy adults of both sexes (18-35 years of age).

Methods: The experimental leg (EXP) will receive the 10 sprays of magnesium oil (20 mg per spray) that will be topically applied to the skin covering the knee extensor muscles, whereas the control leg (CON) will receive 10 sprays of natural mineral-free oil. The vastus lateralis SMcp will be measured by using a tensiomyography (TMG) device before application (PRE) and after 10 (POST10), 20 (POST20), 30 (POST30), 40 (POST40), and 50 (POST50) minutes of application onset, respectively.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

The participants will not be informed about the actual study purpose, while the main investigator will be blinded to the EXP or CON oil administration

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •healthy, recreationally active adults, no history of neuromuscular and musculoskeletal diseases

排除标准

  • •if some of the criteria are not met

研究组 & 干预措施

Experimental

Experimental

Magnesium oil application

干预措施: Magnesium oil (BetterYou) dermal application (Other)

Control

Placebo Comparator

Natural mineral-free oil application

干预措施: Placebo Control (Other)

结局指标

主要结局

Skeletal Muscle Contractile Properties

时间窗: 75 minutes

Skeletal muscle contractile properties will be measured by using tensiomyography device

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Armin Paravlic

Principal Investigator

University of Ljubljana

研究点 (2)

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