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临床试验/NCT02099357
NCT02099357已完成不适用

Creatine or Vitamin D Supplementation in Persons With Spinal Cord Injury Undergoing Resistance Training

Universidade do Porto2 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2014年9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
14
试验地点
2
主要终点
Body Mass Index

研究概览

简要总结

The purpose of this study is to determine the effects of creatine monohydrate or vitamin D supplementation on strength gains following a traditional resistance training program for adults with spinal cord injury.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • •Spinal cord injury
  • •Minimum time since injury: 3 months

排除标准

  • •Participation in resistance training programmes in the previous 6 months
  • •Creatine or vitamin D supplementation in the previous 6 months

研究组 & 干预措施

Placebo

Placebo Comparator

Daily supplementation with 3g of dextrose during eight weeks and placebo ampoules each two weeks.

干预措施: Placebo (Dietary Supplement)

Vitamin D

Active Comparator

Daily supplementation with 3g of dextrose during eight weeks. Vitamin D supplementation, 25000 IU each two weeks.

干预措施: Vitamin D (Dietary Supplement)

Creatine

Experimental

Daily supplementation with 3g of monohydrate creatine during eight weeks. Placebo ampoules each two weeks.

干预措施: Creatine (Dietary Supplement)

结局指标

主要结局

Body Mass Index

时间窗: 8 weeks

Sum of 4 skinfold

时间窗: 8 weeks

Triceps, Biceps, Subscapular and Iliac crest

Corrected Arm Muscle Area

时间窗: 8 weeks

Seated Medicinal Ball Throw

时间窗: 8 weeks

Handgrip Strength with Hand Dynamometer

时间窗: 8 weeks

Manual Wheelchair Slalom Test

时间窗: 8 weeks

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

Samuel Amorim

Bsc

Universidade do Porto

研究点 (2)

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