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临床试验/NCT05041088
NCT05041088Unknown1 期

ProdromeNeuro: A Phase I Study of Omega 3 Oil Nutritional Supplementation for Aging-Related Cognitive Decline

Neurological Associates of West Los Angeles0 个研究点目标入组 40 人开始时间: 2023年6月20日最近更新:
适应症

试验速览

阶段
1 期
入组人数
40
主要终点
Change in ProdromeScan Blood Test

研究概览

简要总结

Aging-related cognitive decline may be affected by brain cholesterol and the health of cell membranes. Certain nutritional supplements have been proposed to support membrane health, and there is increasing interest in plasmalogens and Omega-3 derived oil supplements to support brain health among older adults. Plasmalogens are compounds found in neural cell membranes that are connected to cholesterol processing. Neural cells that have low plasmalogens have shown an inability to process cholesterol properly. Recent research suggests that abnormalities in cholesterol processing and low levels of plasmalogen may play a role in age-related cognitive decline.

The product being investigated in this study is the ProdromeNeuro Omega 3 oil nutritional supplement. This product contains naturally occurring fatty acids in higher concentrations than similar products that are commercially available. The purpose of this research study is to better understand the effects of ProdromeNeuro Omega-3 nutritional supplementation among participants with age-related cognitive decline. It is hoped that taking this product over the course of 4 months will result in improved plasmalogen levels, brain connectivity seen on advanced brain imaging, as well as improved cognitive assessment measurements.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Evidence of a degenerative process
  • Clinical Dementia Rating (CDR) score indicating mild cognitive impairment (CDR = 0.5), mild dementia (CDR = 1) through moderate dementia (CDR = 2)

排除标准

  • Subjects unable to give informed assent
  • Cognitive decline clearly related to an acute illness
  • Advanced terminal illness
  • Any active cancer or chemotherapy
  • Any other neoplastic illness or illness characterized by neovascularity or angiopathy
  • Subjects previously taking plasmalogen supplementation prior to study enrollment

结局指标

主要结局

Change in ProdromeScan Blood Test

时间窗: Change monitored from baseline to 6 month time point (also assessed for change at the end of each month is this time period)

serological testing kit for plasmalogen levels

次要结局

  • Change in Montreal Cognitive Assessment (MoCA)(Change monitored from baseline to 6 month time point (also assessed for change at the end of each month is this time period))
  • Change in Timed 25-foot Walk Test (T25-FW)(Change monitored from baseline to 6 month time point (also assessed for change at the end of each month is this time period))
  • Change in 9-Hole Pegboard Task (9-HPT)(Change monitored from baseline to 6 month time point (also assessed for change at the end of each month is this time period))
  • Change in Timed 25-foot Walk Test Steps (T25-FW)(Change monitored from baseline to 6 month time point (also assessed for change at the end of each month is this time period))
  • Global Rating of Change (GRC)(Assessed at 6 month time point (reflecting on the study))
  • Change in Timed 25-foot Walk Test Speed (T25-FW)(Change monitored from baseline to 6 month time point (also assessed for change at the end of each month is this time period))
  • Change in 30-Second Sit Stand (30CST)(Change monitored from baseline to 6 month time point (also assessed for change at the end of each month is this time period))
  • Change in Quick Dementia Rating Scale (QDRS) used to calculate a Clinical Dementia Rating (CDR) scale(Change monitored from baseline to 6 month time point (also assessed for change at the end of each month is this time period))

研究者

申办方类型
Other
责任方
Sponsor

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