ISRCTN31521726已完成未知
Extended daily fasting, regulation of energy balance and associated health outcomes: a randomised single centre intervention study with two phases
niversity of Bath (UK)0 个研究点目标入组 70 人开始时间: 2010年11月3日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 70
研究概览
简要总结
2011 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/21740575 2014 results in: http://www.ncbi.nlm.nih.gov/pubmed/24898233 2016 results in: http://www.ncbi.nlm.nih.gov/pubmed/26864365 2018 results in: https://www.ncbi.nlm.nih.gov/pubmed/29378040 2019 substudy results in https://www.ncbi.nlm.nih.gov/pubmed/30925197 (added 12/03/2020)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Participants may be male or female (females may or may not be taking oral contraceptives but must maintain a record of menstrual cycle phase or contraceptive use prior to entry into the study)
- •2. Those within the specified age range (20 - 60 years)
- •3. Individuals with a body mass index between 20 - 24 kg/m2 or above 30 kg/m2
- •4. Able and willing to safely comply with all study procedures
- •5. Able to provide written informed consent for participation whilst acknowledging their freedom to withdraw at any point during the study
排除标准
- •1. Women who are known to be pregnant or who are intending to become pregnant over the course of the study
- •2. Women who are breast feeding
- •3. Participation in another clinical trial
- •4. Any reported use of substances which may pose undue personal risk to participants or introduce bias into the experiment
- •5. Any other condition or behaviour deemed either to pose undue personal risk to the participant or introduce bias into the experiment
- •6. Individuals with any known bleeding disorder
- •7. Individuals currently taking any medication known to act as an anticoagulant
研究者
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