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临床试验/NCT04359524
NCT04359524已完成不适用

Fitness and Health Characteristics in Conscripts With Supplementation of Vitamin D

Leho Rips2 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2016年10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
Leho Rips
入组人数
63
试验地点
2
主要终点
Prevalence of vitamin D deficence

研究概览

简要总结

A longitudinal, triple-blinded, randomized, placebo-controlled trial, with a 7-month follow-up period is conducted between October 2016 to April 2017.

详细描述

Body mass (kg) and height (cm) is measured by the same person at the medical center using standardized equipment and the body mass index (BMI) is calculated in kg/m2.

Computed randomization is used to divide conscripts into two groups; either the intervention group or the control group. Both types of capsules are administered once per day in the morning before breakfast for 7 months. Standardized coded packages (3 per conscript) and capsules (100 per package) are manufactured on a special order by Innopharma A/S (Denmark). No commercial sponsoring is involved.

The key of the package code is stored in the computer database until unblinding of the results.

Laboratory measurements Serum samples for clinical chemistry analysis are collected into serum clot activator tubes. Calcium measurements are performed using spectrophotometry method. Ionized calcium measurements are performed using ion selective electrodes. The direct chemiluminescent immunoassay method is used for measurement of PTH. 25(OH)D is measured using direct chemiluminescent immunoassay method.

Power calculation The primary variable of the study is the level of 25 (OH)D in the serum. In the power analysis a difference of 20 nmol/L between the intervention and the control group is considered to be meaningful to detect. If the SD would be 25 nmol/L, then 26 participants would be needed in each group to reach a power of 80%.

研究设计

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

盲法说明

Computed randomization was used to divide conscripts into two groups; either the intervention group, who received vitamin D3 capsules (1200 IU/30µg) or the control group, who received placebo (oil capsules).

入排标准

年龄范围
19 Years 至 27 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • participating in military service at the Estonian Defence Forces
  • voluntarity to participate in the study

排除标准

  • inability to continue military service for any reason, during the 7 month follow-up period

结局指标

主要结局

Prevalence of vitamin D deficence

时间窗: 0, 2, 5 and 7 months of recruitment

Prevalence of vitamin D deficence as measured serum vitamin D 25(OH)D concentration. Vitamin D was considered as sufficient if the se-rum 25(OH)D concentration was ≥75 nmol/L, insufficient if \<75 nmol/L, and deficient if \<50 nmol/L.

次要结局

未报告次要终点

研究者

发起方
Leho Rips
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Leho Rips

Head of department

Tartu University Hospital

研究点 (2)

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