The Effect of Probiotics (L. Helveticus, B. Longum, and B. Bifidum) on Immune Function and Digestive Health



Status:Completed
Conditions:Healthy Studies
Therapuetic Areas:Other
Healthy:No
Age Range:Any
Updated:10/21/2012
Start Date:September 2012
End Date:January 2013
Contact:Bobbi Langkamp-Henken, PhD, RD
Email:henken@ufl.edu
Phone:352-392-1991

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The Effect of Probiotics on Immune Function, and Digestive Health in Academically-stressed University Students: A Randomized, Double-blinded, Placebo-controlled Study


The purpose of this study is to determine if daily consumption of a probiotic in the period
before, during and after academic exams will help maintain digestive and immune health and
quality of life of undergraduate students.


A randomized, double-blinded, placebo-controlled trial will be used. Healthy full-time
undergraduate students will be recruited from the University of Florida via flyers, emails,
announcements, etc. Informed consent will be obtained and the inclusion/exclusion criteria
will be reviewed to determine whether a participant qualifies for the study. All
participants will be consented for the main six-week intervention and a subgroup
(n=50/group) of these students will be consented to provide two stool samples.

Participants will provide saliva and stool samples (for the sub-group)during the
pre-baseline week and during the week of final exams at approximately week 4. At the
randomization visit, height, weight and age will be obtained. Participants will be
stratified based on body mass index and randomized via sealed envelopes to one of four
groups: Lactobacillus helveticus, Bifidobacterium longum ssp. Infantis, Bifidobacterium
bifidum or the placebo (n=145/group). Participants will take the study provided capsule of
probiotic or placebo daily for 6 weeks. Participants will receive daily questionnaires via
email throughout the prebaseline week and the 6-week intervention. Daily questionnaires will
ask about intake of the supplement, cold symptoms, and general health (i.e., new
medications, doctor visits). Throughout the study, participants will also be asked to
complete weekly questionnaires (inquiring about gastrointestinal symptoms and physical
activity) and Quality of Life Questionnaires (administered during pre-baseline, final exam
week and week 6 of the study).

Inclusion Criteria:

To participate in the study you must:

- be 18 years of age or older.

- be a healthy full-time undergraduate at the University of Florida.

- be willing to complete daily questionnaires form via computer.

- be willing to discontinue any immune-enhancing dietary supplements (e.g., prebiotics
and fiber supplements, probiotics, echinacea, fish oil, vitamin E >400% of the RDA or
>60 mg/day).

- be willing to take the probiotic capsule daily of 6 weeks.

- have had at least one cold in the last 12 months.

- have at least 1 final during the scheduled exam week.

- have daily access to the Internet.

Exclusion Criteria:

To participate in the study you must NOT:

- be a current smoker.

- have chronic allergies involving the upper respiratory tract.

- have had immunosuppressive illness or treatment within the last year.

- have received antibiotic therapy in the past two months.
We found this trial at
1
site
Gainesville, Florida 32610
(352) 392-3261
University of Florida The University of Florida (UF) is a major, public, comprehensive, land-grant, research...
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