The Effect of a Probiotic Strain on Stress-related Intestinal Hyperpermeability in Adult Humans.
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 117
- Locations
- 1
- Primary Endpoint
- Lactulose-Mannitol Ratio (LMR) during the stress condition vs. baseline
Study Overview
Brief Summary
This is a single-site exploratory study aiming to demonstrate the effect of a fresh fermented dairy drink containing a probiotic strain on stress-related intestinal hyperpermeability in students defending a bachelor's or master's thesis in front of a jury at the University of Leuven (Belgium).
Detailed Description
The study is conceived as a single-site exploratory study with a randomized, controlled, parallel group design. There will be a double blind with 2 intervention arms (Test product with probiotic and acidified milk Control) plus an extra open label arm without intervention in a 2:2:1 ratio. The goal of the open-label arm is to confirm our previous data on the effect of stress on small intestinal permeability (see reference), without powering the study to detect a significant difference within this open-label arm. The participants and the investigators are blinded to the allocation to the probiotic vs. acidified milk control arm. However, there is no blinding in the arm without intervention.
In vivo intestinal permeability and salivary markers of psychological stress and activation of the autonomous nervous system will be measured and questionnaires will be completed at 4 different test days: baseline (V2), two weeks after randomization (V3), during an oral defense of a master's or bachelor's thesis (V4) and finally after pretreatment with Indomethacin (V5).
The 5 study visits are organized around the thesis defence (D0):
V1 (screening + inclusion) takes place within 2 to 3 weeks prior to the randomization.
V2 (baseline + randomization) will take place between D-35 to D-27. V3 (randomization + 2 weeks) will take place at D-14 +/-1day. V4 (thesis defense) is D0 and organized by the University. V5 (Indomethacin) will take place at D+14 +/-1day.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Investigator)
Masking Description
double blind only in Test and Control arm open label in arm without intervention
Eligibility Criteria
- Ages
- 20 Years to 30 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Student defending a bachelor's or master's thesis in front of a jury
- •Age 20 till 30 years (both included), both genders
- •Subject, upon briefing of the content of the present study, fully understanding and agreeing to its objective and having given written (dated and signed) informed consent form to take part in the study
- •Subject willing to consume 2 units of investigational product per day during the investigational product consumption period.
- •For females: If of child bearing potential, female subjects must be using or complying with methods of contraception
- •Subject willing to strictly follow dietary/medication instructions for the entire duration of the study
- •Subject must have access to a refrigerator with adequate space to store the investigational products according to the labels' storage recommendations and a freezer for the cooling elements in the transport bag
Exclusion Criteria
- •Subject with chronic gastrointestinal disorders or symptoms, type 1 or type 2 diabetes mellitus, psychiatric disease including but not limited to depression (screened by PHQ-9) and general anxiety disorder (screened by GAD-7), celiac disease, food allergy or a history of atopic conditions (eczema, allergic asthma, allergic rhinoconjunctivitis) requiring active treatment
- •Subject with allergy or intolerance to non-steroidal anti-inflammatory drugs (NSAID)
- •Subject with first degree relatives with coeliac disease, inflammatory bowel disease (IBD) or type 1 diabetes
- •Subject with known or suspected lactose intolerance or suspected allergy or hypersensitivity to any component of the study product(s) (e.g. milk protein)
- •Subject receiving (currently or in the 2 last weeks) systemic treatment or topical treatment likely to interfere with evaluation of the study parameters: antibiotics, intestinal or respiratory antiseptics, anti-rheumatics, NSAIDs and steroids prescribed in chronic inflammatory diseases.
- •Active smoker with at least 7 cigarettes per week
- •Subject consuming regularly (>1/week) more than 3 units of alcohol per day.
Arms & Interventions
Test product
Fresh fermented dairy drink containing probiotic strain consumed as follows: one bottle (100g) BID for 6 weeks
Intervention: Fresh fermented dairy drink containing probiotic strain (Dietary Supplement)
Control product
Acidified dairy drink without ferment consumed as follows: one bottle (100g) BID for 6 weeks
Intervention: Acidified dairy drink without ferment (Other)
No product
no product
Outcomes
Primary Outcomes
Lactulose-Mannitol Ratio (LMR) during the stress condition vs. baseline
Time Frame: oral administration of Test or Control product for 4 weeks before stress condition
LMR or in vivo small intestinal permeability during stress condition vs. baseline in the Test product with probiotic compared to the acidified milk Control arm
Secondary Outcomes
- Salivary cortisol during the stress condition vs. baseline(oral administration of Test or Control product for 4 weeks before stress condition)
- LMR after indomethacin vs. baseline(oral administration of Test or Control product for 6 weeks before indomethacin)
- LMR during administration of Test or Control product vs. baseline(oral administration of Test or Control product for 2 weeks)
- Subjective anxiety levels (STAI state) during the stress condition vs. baseline(oral administration of Test or Control product for 4 weeks before stress condition)