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临床试验/NCT01877967
NCT01877967Unknown不适用

A Randomised Double-blind Placebo-controlled Trial Investigating the Effect of Dietary Supplement VSL#3 on Memory, Attention, Executive Function and Mood in Healthy Older Adults.

University of Dublin, Trinity College1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2013年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
80
试验地点
1
主要终点
Changes in cognition

研究概览

简要总结

This research aims to determine whether a 12 week daily dose of VSL#3 has any measurable effects on memory, attention, executive function or self-reported mood and anxiety in healthy older adults.

详细描述

This research aims to investigate the effect of dietary supplement VSL#3 on memory, attention, executive function and mood in healthy older adults.

The study will be a randomised double-blind placebo-controlled design and eighty participants will be recruited to take part. Forty participants will be randomly allocated to the food supplement and 40 to placebo. As the sample is initially self-selecting where individuals volunteer to take part, a minimisation procedure will be used to randomise group allocation (Altman & Bland, 2005), with volunteers stratified by gender. Neither the participant nor the research assistant supplying the supplement will know which preparation is administered, thus ensuring double-blind administration.

Participants will be asked to take the food supplement daily for 12 weeks and the pre- and post- intervention data will be collected immediately before and after this time period.

Both pre- and post-intervention data will be collected using validated neuropsychological measures, cognitive measures, EEG and self-report questionnaires. Blood sampling will be conducted pre- and post-intervention by a Research Assistant trained in phlebotomy. Analysis will be carried out on each of the measures using a two-way ANCOVA, using the pre-treatment score as covariate.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
65 Years 至 75 Years(Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Aged between 65 and 75
  • •MMSE score > 23
  • •Willingness to give informed consent
  • •Commitment to take the VSL#3 supplement daily for 12 weeks
  • •Alcohol consumption less than 21 units per week (men), 14 units per week (women)

排除标准

  • •Current psychoactive medication
  • •Significant active medical conditions
  • •History of major psychiatric or neurological condition
  • •History of epilepsy
  • •History of traumatic brain injury
  • •History of immunodeficiency
  • •Taking immunosuppressants or corticosteroids

研究组 & 干预措施

Intervention

Experimental

This group will intake the recommended daily amount of the food supplement VSL#3 (two sachets of the supplement in powder form) every day for twelve weeks. The two sachets will either be taken together or one in the morning and one in the evening.

干预措施: VSL#3 (Dietary Supplement)

Placebo

Placebo Comparator

This group will intake two sachets (2x4.4g) of a placebo each day for 12 weeks. The placebo is in the same powdered form as the food supplement taken by the intervention group. The two sachets will either be taken together or one in the morning and one in the evening.

干预措施: placebo (Dietary Supplement)

结局指标

主要结局

Changes in cognition

时间窗: Pre and Post the 12 week Intervention

Measures used to assess cognition: Mini Mental State Exam National Adult Reading Test Free and Cued Selective Reminding Test (FCSRT) Category Fluency Task (Animal Fluency) Colour Trials test 1 \& 2 Sustained Attention Response Task Choice Reaction Time Task Prospective Memory Task Self-Rated Memory Electrophysiological Measures (EEG spectral power - alpha range 8-14Hz)

次要结局

  • Changes in Mood(Pre and Post the 12 week Intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Brian Lawlor

Professor

University of Dublin, Trinity College

研究点 (1)

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