跳至主要内容
临床试验/NL-OMON27586
NL-OMON27586尚未招募不适用

Bone health in professional cycling

HAN University of Applied Sciences0 个研究点目标入组 75 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
75

研究概览

简要总结

ot applicable

研究设计

研究类型
Observational

入排标准

入选标准

  • Inclusion criteria
  • World tour level (highest level) professional male cyclists (aged 22 – 40):
  • Professional cyclist competing in UCI’s WorldTour competition
  • Willing to give written informed consent.
  • Willing to comply with study procedures.
  • Accept use of all encoded data, including publication, and the confidential use and storage of all data for 15 years.
  • World tour level professional female cyclists (aged 22 – 40):
  • Professional cyclist competing in UCI’s Women’s WorldTour competition
  • Willing to give written informed consent.
  • Willing to comply with study procedures.
  • Accept use of all encoded data, including publication, and the confidential use and storage of all data for 15 years.
  • Talented elite male cyclist (aged 18 – 22):
  • Included in a talent program of professional cycling team
  • Willing to give written informed consent.
  • Willing to comply with study procedures.
  • Accept use of all encoded data, including publication, and the confidential use and storage of all data for 15 years.
  • Retired world tour level professional cyclists (aged 35 – 60):
  • Retired male of female professional cyclist.
  • A minimum of 5 years of professional cycling at WorldTour level.
  • Duration of retirement is minimal 1 year before Day 01 of this study.
  • Willing to give written informed consent.
  • Willing to comply with study procedures.
  • Accept use of all encoded data, including publication, and the confidential use and storage of all data for 15 years.

排除标准

  • Exclusion criteria
  • Having a history of medical events or medication use that may significantly affect bone metabolism, to be decided by the principal investigator.
  • Medication use that may affect tests within this study must be minimal 3 months before Day 01 of this study.
  • Participation in any clinical trial including blood sampling and/or administration of substances up to 30 days before Day 01 of this study
  • A recent injury that may significantly affect BMD, to be decided by the principal investigator.

研究者

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