ISRCTN79265514已完成未知
A randomised clinical trial of vitamin D to improve cognition in people at risk of dementia
niversity of Exeter0 个研究点目标入组 685 人开始时间: 2018年7月23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
- 685
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Current inclusion criteria as of 23/04/2020:
- •1. Age 50 and over
- •2. Already registered as a participant on the PROTECT study
- •3. Fulfilling research criteria for dementia risk: Either (1) Performing at least one Standard Deviation below age-matched population norms in two cognitive tests as measured using the validated PROTECT and online cognitive test battery; and/or (2) Reporting subjective memory concerns; and/or (3) Reported family history of dementia
- •4. Fulfilling criteria for vitamin D deficiency risk: Defined by a self-reported scale to be completed on registration.
- •5. Access to a computer and the internet.
- •Previous inclusion criteria:
- •1. Aged 50 years and over
- •2. Already registered as a participant on the PROTECT study
- •3. Fulfilling the AACD criteria: performing at least standard deviation below age-matched population norms in two cognitive tests, as measured using the validated PROTECT and CogTrackTM online cognitive test batteries
- •4. Fulfilling criteria for vitamin D deficiency risk (defined by a self-reported scale to be completed upon registration (based on Annweiler et al., 2017)
- •5. Access to a computer and the internet
排除标准
- •1. Diagnosed with dementia
- •2. Already participating in another active interventional clinical trial
- •3. Regularly taking any supplement containing vitamin D:
- •3.1. If the supplement is prescribed for a pre-existing condition, the participant will be excluded
- •3.2. If the supplement is bought over the counter, the participant will have the option of stopping the supplement and re-registering for the trial after a 28 day washout period
- •4. Prescribed the medication Digoxin (Lanoxin)
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