Fitness and Health Characteristics in Conscripts With Supplementation of Vitamin D
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
- 是
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
Leho Rips
Head of department
Tartu University Hospital
