Skip to main content
Clinical Trials/NCT01657643
NCT01657643CompletedNot Applicable

Effect of Lactobacillus Rhamnosus LGG® and Bifidobacterium Animalis Ssp Lactis BB-12® on Health-related Quality of Life in College Students With Upper Respiratory Infections

University of Medicine and Dentistry of New Jersey1 site in 1 country231 target enrollmentStarted: January 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
231
Locations
1
Primary Endpoint
Health-related quality of life

Study Overview

Brief Summary

The main purpose of the study is to find out if probiotics (healthy bacteria found in yogurt) can improve the health-related quality of life (HRQL) during upper respiratory infections (like the common cold) in college students living in residence hall on-campus at Framingham State University (Framingham, MA) who are randomized to receive a probiotic or placebo candy daily for 12 weeks. HRQL is a subjective measure, defined as the aspects of quality of life (i.e., one's satisfaction with their life) that related specifically to a person's health (for example, ability to carry out normal daily activities). The investigators hypothesize that HRQL during URIs will be significantly higher in the probiotic groups compared to the placebo group. The proposed study will also seek to address the following secondary objectives: missed school and work days due to a upper respiratory infection.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 25 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Student at Framingham State University (Framingham, MA)
  • •Live in on-campus housing

Exclusion Criteria

  • •their driver's license or state identification card indicated that they were under 18 years of age or over 25 years of age;
  • •they experienced chronic perennial allergies (such as, allergies to dust or 3) they were pregnant
  • •4) they had been diagnosed with medical conditions affecting immune function (for example, asthma, chronic fatigue syndrome and human immunodeficiency virus) 5) they had acute pancreatitis, were undergoing treatment for cancer; or, were taking immunosuppressive drugs for an autoimmune disease or post-transplant.

Arms & Interventions

Probiotics

Experimental

Every day for 12 weeks, subjects are asked to eat 5 grams of a strawberry-flavored candy that contains probiotics [daily dose minimum of 1 billion CFU of each Lactobacillus rhamnosus LGG® (LGG®), and Bifidobacterium animalis ssp lactis BB-12® (BB-12®)]

Intervention: Probiotics (Dietary Supplement)

Placebo

Placebo Comparator

Every day for 12 weeks, subjects are asked to eat 5 grams of a placebo (strawberry-flavored candy powder)

Intervention: placebo (Dietary Supplement)

Outcomes

Primary Outcomes

Health-related quality of life

Time Frame: 12 weeks

Subjects are asked to complete a questionnaire every day for 12 weeks that inquires about any common cold symptoms that they may be experiencing, severity of the symptoms, and how the symptoms interfere with their daily activities. Health-related quality of life is operationalized by total score on the questionnaire.

Secondary Outcomes

  • Missed work days(Once per week over the course of 12 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

SHRP nutritional sciences

Tracey J. Smith, Doctoral Student

Rutgers, The State University of New Jersey

Study Sites (1)

Loading locations...

Similar Trials