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The Effects of Probiotic Supplementation on State and Trait Stress, Anxiety, and Depression Symptoms in Stressed Adults

U

University of Colorado Boulder (CU)

Status

Completed

Conditions

Depressive Symptoms
Anxiety Symptoms
Perceived Stress

Treatments

Dietary Supplement: Lactobacillus reuteri DSM 17938
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT07216729
22-0234

Details and patient eligibility

About

The goal of this randomized controlled trial is to learn if supplementation with the probiotic Lactobacillus reuteri DSM 17938 can reduce levels of trait and state perceived stress, anxiety, and depressive symptoms compared to a placebo in a population of stressed adults ages 18-45. This study also investigates several evidence-based moderators of treatment effects, evaluates whether the probiotic caused side effects, and evaluates whether effects endured at 1-month post-supplementation.

Enrollment

150 patients

Sex

All

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age 18 - 45
  • scoring 14+ on the perceived stress scale-10 indicating medium stress or higher
  • ability to provide informed consent
  • willingness not to take probiotic supplements (pills, tablets, oils, etc.) other than the product provided in the clinical study until all study procedures are completed
  • own a smartphone and are willing to receive study materials and complete study procedures by text

Exclusion criteria

  • a history of gastrointestinal discomfort or surgery, urinary incontinence, cancer, toxic shock syndrome, frequent diarrhea, vital signs outside of the acceptable range (i.e., blood pressure >160/100, oral temperature >100°F, pulse >100), heart disease, heart attack, lung/respiratory disease, any pulmonary, cardiovascular, gastrointestinal, hepatic or renal functional abnormality (i.e. a medical diagnosis related to lungs, heart, stomach/intestines, liver, or kidneys), HIV, Hepatitis B, Hepatitis C, bipolar disorder, psychosis, or confirmed or suspected immunosuppression or immunodeficiency
  • current (past month) alcohol or substance abuse or dependence (score of 2+ on the UNCOPE)
  • consistent (e.g., 5x/week or greater) probiotic supplementation within the last month, including probiotic food products such as yogurt
  • receiving antibiotics within the last month
  • receiving medications that interfere with gut motility (opiates, loperamide, stool softeners)
  • use of systemic antibiotics, antifungals, antivirals, or antiparasitics (intravenous, intramuscular, or oral)
  • use of oral, intravenous, intramuscular, nasal or inhaled corticosteroids
  • use of cytokines or cytokine inhibitors
  • use of methotrexate or immunosuppressive cytotoxic agents
  • receiving immunosuppressive drugs/medications or treatment including antineoplastic therapy, post-transplantation immunosuppressive therapy, and/or radiation therapy
  • participation in conflicting interventional research protocol
  • unstable dietary history as defined by major changes in diet during the previous month, where the subject has eliminated or significantly increased a major food group in their diet
  • female who is pregnant or lactating or reports expecting to get pregnant during the course of the study
  • currently involved in the criminal justice system as a prisoner or ward of the state

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

150 participants in 2 patient groups, including a placebo group

Probiotic
Experimental group
Description:
5 drops daily (100 million colony-forming units) for 46 days of Lactobacillus reuteri DSM 17938 in sunflower oil, medium chain triglyceride oil, and silicon dioxide.
Treatment:
Dietary Supplement: Lactobacillus reuteri DSM 17938
Placebo
Placebo Comparator group
Description:
5 drops daily for 46 days of a placebo consisting of the inactive ingredients from the probiotic supplement, specifically sunflower oil, medium chain triglyceride oil, and silicon dioxide.
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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