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临床试验/NCT01662206
NCT01662206已完成不适用

Probiotics (Lactobacillus Gasseri, Bifidobacterium Bifidum, Bifidobacterium Longum) on Immune and Intestinal Health in Healthy Older Adults

University of Florida2 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2012年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
46
试验地点
2
主要终点
Change in cytokine production

研究概览

简要总结

The purpose of this study is to determine whether healthy older adults, aged 65 to 80 years, consuming a probiotic each day for three weeks will have improved immune strength and digestive health. It is hypothesized that older adults consuming the probiotics will see a shift in their microbiota towards the "healthy" bacteria resulting in a greater proportion of immune cells, decreased inflammation, and better digestive health.

详细描述

This is a randomized, double-blind, placebo controlled crossover design with two 3-week interventions and a 5-week washout period in between. Thirty-six participants will be enrolled. With informed consent, the daily questionnaire will be administered and a baseline stool sample will be obtained during the week before the start of each intervention period. Blood and saliva will be collected on the first and last day of each intervention period to assess immune function. A final stool sample will be obtained in the last week of the intervention period. Nutritional status, which can impact immune function, will be assessed using the Mini-Nutritional Assessment, Block Fiber Screen, and the Block 2005 Food Frequency Questionnaire. Daily questionnaires will record intake of the probiotic or placebo, level of stress, hours of sleep, visits to the physician, new medications, number of stools, etc. The Gastrointestinal Symptom Response Scale, which records gastrointestinal symptoms, such as bloating, gas, diarrhea, and constipation, over the past week will be completed at baseline and weekly during the interventions and the week following the interventions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • 65 to 80 years of age.
  • willing and able to complete the Informed Consent Form in English
  • willing to provide demographic information (age, race)
  • willing and able to complete daily and weekly questionnaires regarding general wellness, bowel function and gastrointestinal symptoms.
  • willing to provide 4 blood, 4 stool, and 4 saliva samples
  • willing to discontinue any immune-enhancing dietary supplements ( e.g., prebiotics supplements, Echinacea, fish oil, vitamin E >200% of the RDA).
  • able to take the study probiotic without the aid of another person.

排除标准

  • not meet the above criteria.
  • taking any medication for constipation or diarrhea.
  • currently taking any anti-inflammatory drugs on a regular basis.
  • current smoker.
  • typically consume fermented foods or probiotics (e.g., yogurts with live, active cultures or supplements).
  • currently being treated for or have any of the following physician- diagnosed diseases or conditions: HIV/AIDS, immune modulating diseases (autoimmune, hepatitis, cancer, etc.), kidney disease, diabetes or gastrointestinal disease or conditions (such as ulcerative colitis, Crohn's disease, gastroparesis, cancer, peptic ulcer disease, Celiac disease, short bowel disease, ileostomy, colostomy) other than GERD or diverticular disease or have a central venous catheter.
  • received chemotherapy or other immune suppressing therapy within the last year.
  • received antibiotic therapy in the past two months.
  • cannot schedule planned immunizations to at least 4 weeks before the start of the study, in the week following the second blood draw, or after the 4th blood draw.

结局指标

主要结局

Change in cytokine production

时间窗: Measured at baseline and after 3 weeks of supplementation for each arm

Peripheral blood mononuclear cell cytokine production following lipopolysaccharide stimulation

Change in bacterial species measured in fecal samples

时间窗: Measured at baseline and after 3 weeks of supplementation for each arm

* Microbial diversity measured by 454 16S rRNA sequence analysis * qPCR to quantify changes in bacteria of interest

次要结局

  • Change in digestive symptoms on the Gastrointestinal Symptom Response Scale(Measured at baseline, weeks 1, 2, 3 and 4 of each arm)
  • Change in Mucosal immune function(Measured at baseline and after 3 weeks of supplementation for each arm)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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