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临床试验/NCT07646054
NCT07646054尚未招募不适用

Wellderly Brain - Alzheimer's Disease Prevention With Lifestyle Coaching Intervention: A Randomized Clinical Trial

Scripps Translational Science Institute1 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2026年7月6日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
1,200
试验地点
1

研究概览

简要总结

Wellderly Brain is a randomized, direct-to-participant trial evaluating whether a virtually delivered, multidomain lifestyle coaching intervention can favorably impact plasma biomarkers of Alzheimer's disease (AD) in adults aged 60-80 with APOE4 positivity or elevated polygenic risk. Participants are recruited through 23andMe and enrolled via the MyDataHelps platform. Following genetic eligibility screening, 1,200 participants will be randomized to either a digital lifestyle coaching arm (UCardia) or an education-only control arm. The intervention consists of 16 virtual coaching sessions delivered over 52 weeks. All participants will wear an Oura Ring for continuous health monitoring and provide dried blood samples at baseline, 6 months, and 12 months for plasma p-tau217 and proteomic profiling via the NULISAseq CNS Disease Panel. Saliva samples will be collected for epigenetic aging analysis. The study duration is 14-16 months per participant.

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
None

入排标准

年龄范围
60 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Current 23andMe Research participant with APOE4 positivity genetic variant
  • Age 60 to 80 at time of consent
  • Have access to an Android or Apple iPhone smartphone device and able to download study apps
  • Lives in the United States and able to send and receive US Mail
  • Able and willing to perform a self-administered saliva test at screening*for organic outreach only.
  • Able and willing to perform a self-administered finger prick blood collection at three time points throughout the study.

排除标准

  • Non-English speaking
  • Lives outside of the United States
  • Currently taking or planning on taking GLP-1 medications (Exenatide, Liraglutide, Albiglutide, Dulaglutide, Semaglutide or Tirzepatide) within the next 12 months
  • Established diagnosis of Mild Cognitive Impairment, Alzheimer's Disease or other Neurodegenerative Disease (Parkinson's Disease, Amyotrophic Lateral Sclerosis, Huntington's Disease, Multiple Sclerosis or Frontotemporal Dementia).
  • Current or past Oura Ring user (any Oura Ring use in the last 12 months)

研究者

发起方
Scripps Translational Science Institute
申办方类型
Other
责任方
Sponsor

研究点 (1)

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