Effects of Probiotics on Mood
Primary Purpose
Depression, Anxiety
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Bifihappy
Placebo
Sponsored by

About this trial
This is an interventional treatment trial for Depression, Anxiety
Eligibility Criteria
Inclusion Criteria:
- Male and Famale subjects.
- Aged between 18 and 35.
- Already owing a smartphone with Android or iOS system.
Exclusion Criteria:
- Drug taking, smoking, coeliac disease, lactose intolerance.
- Disorders such as IBS (Irritable Bowel Syndrome), IBD (Irritable Bowel Disease), UC (Ulcerative Colitis) and other serious diseases, e.g. MS (Multiple Sclerosis) and diabetes (type 1/type 2).
- Oral intake of antibiotics and other medicines on a continuative basis.
Sites / Locations
- University of Verona
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Group 1
Group 2
Arm Description
the subjects are treated with probiotics: Bifihappy
the subjects are treated with a placebo
Outcomes
Primary Outcome Measures
Change in the psychological profile
The primary outcome is the difference in the scores at the Leiden Index of Depression Sensitivity-Revised test (LEIDS-R) standardized questionnaire between the experimental and control groups. The Leiden Index of Depression Sensitivity-Revised test, LEIDS-R, is a self-report questionnaire that tests cognitive reactivity to sad mood, which is an index of cognitive vulnerability to depression.
Secondary Outcome Measures
Evaluation of mood - State Trait Anxiety Inventory (STAI) standardized questionnarie.
difference in the scores between the experimental and control groups. The State Trait Anxiety Inventory, STAI, is a self-report questionnaire that measures the presence and severity of current symptoms of anxiety and the propensity to be anxious.
Evaluation of mood - Beck Depression Inventory (BDI-2) standardized questionnarie.
difference in the scores between the experimental and control groups. The Beck Depression Inventory, BDI-2, is a self-report questionnaire that measures the occurrence and severity of current depressive symptoms.
Evaluation of mood - Profile od Mood State (POMS) standardized questionnarie.
difference in the scores between the experimental and control groups. The Profile of Mood State, POMS, is a self-report questionnaire that assesses mood.
Evaluation of the quality of sleep.
difference in the scores between the experimental and control groups in the standardized questionnaire Pittsburgh Sleep Quality Index (PSQI). The Pittsburgh Sleep Quality Index, PSQI, is a self-report questionnaire that assesses sleep quality for the majority of days and nights in the past months.
Evaluation of personality - Temperament and Character Inventory (TCI) standardized questionnarie.
difference in the scores between the experimental and control groups. The Temperament and Character Inventory, TCI, is a self-report, true-false questionnaire that measures two components of personality: temperament and character.
Evaluation of personality - Cope Orientation to Problem Experienced-New Italian Version (COPE-NIV) standardized questionnarie.
difference in the scores between the experimental and control groups. The Cope Orientation to Problem Experienced - New Italian Version, COPE-NIV, is a self-report questionnaire that measures coping strategies: the cognitive and behavioral strategies people use to manage stressful situations.
Evaluation of personality - Behavioral Inhibition System and Behavioral Activation System Scale (BIS/BAS) standardized questionnarie.
difference in the scores between the experimental and control groups. The Behavioral Inhibition and Behavioral Activation Scale, BIS/BAS, is a self-report questionnaire that measures an individual's sensitivity to behavioral inhibition and behavioral activation systems.
Evaluation of personality - Life Orientation Test-revisited (LOT-R) standardized questionnarie.
difference in the scores between the experimental and control groups. The Life Orientation Test-revisited, LOT-R, is a self-report measure of dispositional optimism and pessimism.
Full Information
NCT ID
NCT03539263
First Posted
April 6, 2018
Last Updated
May 25, 2018
Sponsor
Probiotical S.p.A.
Collaborators
Universita di Verona
1. Study Identification
Unique Protocol Identification Number
NCT03539263
Brief Title
Effects of Probiotics on Mood
Official Title
Randomized Controlled Experimental Trial Designed to Test the Effects of Probiotics on Mood
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
December 20, 2016 (Actual)
Primary Completion Date
June 15, 2017 (Actual)
Study Completion Date
June 15, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Probiotical S.p.A.
Collaborators
Universita di Verona
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Recent demonstration that probiotics administration has positive effects on depressive feelings in healthy populations suggests its possible role as an adjuvant therapy for depression in clinical populations and as a non-invasive strategy to prevent depressive feelings in healthy individuals. The present study extends current knowledge on the beneficial effects of probiotics on psychological well-being, as measured by changes in mood (e.g., depression, anxiety, cognitive reactivity to sad mood), personality dimensions, and quality of sleep, which have been considered as related to mood. For this double-blind, placebo-controlled study healthy volunteers pseudo-randomly assigned to an experimental or control group assumed a daily dose of probiotic or placebo, respectively, for 6 weeks. Mood, personality dimensions, and sleep quality were assessed four times (before the beginning of the study, at 3 and 6 weeks, and at 3 weeks of washout).
Detailed Description
A. THEORETICAL BACKGROUND The intestine and the brain are intimately connected with each other through the gut-brain axis, which involves bidirectional communication between the nervous, endocrine and immune systems. In the last years, it has become increasingly evident that this communication implies also interactions with the intestinal bacterial flora, which releases immune activation and other signalling molecules that may play a major role in the regulation of the brain and human behaviour. For instance, the microbiota produces neuroactive substances and their precursors (e.g. tryptophan) that may reach the brain through the endocrine and autonomous nervous system. Recently, the interest has been focused also on the cognitive field. Indeed, there is experimental evidence that bacterial products may positively influence cognitive functions, such as spatial memory and problem-solving abilities. Moreover, probiotics seem to exercise influence on mood, anxiety and depression, opening new therapeutic prospects. A recent trial showed that four weeks of taking probiotics (Bifidobacterium bifidum W23, Bifidobacterium lactis W52, Lactobacillus acidophilus W37, Lactobacillus brevis W63, Lactobacillus casei W56, Lactobacillus salivarius W24, Lactococcus lactis W19 e W58) led to an improvement in mood, fostering reduction in negative thoughts.
B. THE PURPOSE OF THE RESEARCH PROJECT The primary goal of the trial is to investigate the effect of probiotics on depression. Moreover, it will assess also effects on anxiety and other personality traits in healthy young students. The trial intends also to investigate whether probiotics may influence the quality of sleep and bowel habits. The trial will be placebo-controlled, randomized, pre- and post-intervention, double-blind designed (investigator and participants). In the light of the several end-points examined, the statistical analysis will be of explorative type.
The collection of faecal samples will allow, in case of finding any effects of the administered product on mood, to go back to any microbial components that have changed in individuals following the treatment. Monitoring (see below) the normal feed and physical habits of the individuals will allow to check the possible effect of these confounding factors on the parameters measured in the trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Anxiety
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The trial design is parallel, with two groups (experimental group and control group) and four evaluation sessions at intervals of three weeks (T0wk = baseline, T3wk = intermediate, T6wk=final and T9wk = follow-up).
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
39 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group 1
Arm Type
Experimental
Arm Description
the subjects are treated with probiotics: Bifihappy
Arm Title
Group 2
Arm Type
Placebo Comparator
Arm Description
the subjects are treated with a placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Bifihappy
Intervention Description
During the six weeks of treatment, the experimental group will take daily doses of 2,5 g with a concentration of 4x109 CFU/sachet of a mixture of lyophilised probiotic strains of the following species:
Lactobacillus fermentum
Lactobacillus rhamnosus
Lactobacillus plantarum
Bifidobacterium longum
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
During the six weeks of treatment, the experimental group will take daily doses of 2,5 g of maltodextrin
Primary Outcome Measure Information:
Title
Change in the psychological profile
Description
The primary outcome is the difference in the scores at the Leiden Index of Depression Sensitivity-Revised test (LEIDS-R) standardized questionnaire between the experimental and control groups. The Leiden Index of Depression Sensitivity-Revised test, LEIDS-R, is a self-report questionnaire that tests cognitive reactivity to sad mood, which is an index of cognitive vulnerability to depression.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
Secondary Outcome Measure Information:
Title
Evaluation of mood - State Trait Anxiety Inventory (STAI) standardized questionnarie.
Description
difference in the scores between the experimental and control groups. The State Trait Anxiety Inventory, STAI, is a self-report questionnaire that measures the presence and severity of current symptoms of anxiety and the propensity to be anxious.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
Title
Evaluation of mood - Beck Depression Inventory (BDI-2) standardized questionnarie.
Description
difference in the scores between the experimental and control groups. The Beck Depression Inventory, BDI-2, is a self-report questionnaire that measures the occurrence and severity of current depressive symptoms.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
Title
Evaluation of mood - Profile od Mood State (POMS) standardized questionnarie.
Description
difference in the scores between the experimental and control groups. The Profile of Mood State, POMS, is a self-report questionnaire that assesses mood.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
Title
Evaluation of the quality of sleep.
Description
difference in the scores between the experimental and control groups in the standardized questionnaire Pittsburgh Sleep Quality Index (PSQI). The Pittsburgh Sleep Quality Index, PSQI, is a self-report questionnaire that assesses sleep quality for the majority of days and nights in the past months.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
Title
Evaluation of personality - Temperament and Character Inventory (TCI) standardized questionnarie.
Description
difference in the scores between the experimental and control groups. The Temperament and Character Inventory, TCI, is a self-report, true-false questionnaire that measures two components of personality: temperament and character.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
Title
Evaluation of personality - Cope Orientation to Problem Experienced-New Italian Version (COPE-NIV) standardized questionnarie.
Description
difference in the scores between the experimental and control groups. The Cope Orientation to Problem Experienced - New Italian Version, COPE-NIV, is a self-report questionnaire that measures coping strategies: the cognitive and behavioral strategies people use to manage stressful situations.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
Title
Evaluation of personality - Behavioral Inhibition System and Behavioral Activation System Scale (BIS/BAS) standardized questionnarie.
Description
difference in the scores between the experimental and control groups. The Behavioral Inhibition and Behavioral Activation Scale, BIS/BAS, is a self-report questionnaire that measures an individual's sensitivity to behavioral inhibition and behavioral activation systems.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
Title
Evaluation of personality - Life Orientation Test-revisited (LOT-R) standardized questionnarie.
Description
difference in the scores between the experimental and control groups. The Life Orientation Test-revisited, LOT-R, is a self-report measure of dispositional optimism and pessimism.
Time Frame
four evaluation sessions at intervals of three weeks of probiotic intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Male and Famale subjects.
Aged between 18 and 35.
Already owing a smartphone with Android or iOS system.
Exclusion Criteria:
Drug taking, smoking, coeliac disease, lactose intolerance.
Disorders such as IBS (Irritable Bowel Syndrome), IBD (Irritable Bowel Disease), UC (Ulcerative Colitis) and other serious diseases, e.g. MS (Multiple Sclerosis) and diabetes (type 1/type 2).
Oral intake of antibiotics and other medicines on a continuative basis.
Facility Information:
Facility Name
University of Verona
City
Verona
ZIP/Postal Code
37131
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Study Protocol
IPD Sharing Time Frame
from April 2018
IPD Sharing Access Criteria
Plos One
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Effects of Probiotics on Mood
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