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Probiotic Administration on Mood (PAM)

Primary Purpose

Depression, Sleep, Stress

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Probiotic
Sponsored by
Lindenwood University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Depression

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • between the ages of 18 - 50 years
  • has a body mass index between 18.5 - 30 kg/m2.
  • Anyone with a body mass index between 30 - 32 kg/m2, but has a body composition <25% fat -for men and <35% for women will be accepted into the study
  • has been weight stable for the past three months (defined as less than a 5% variation in body -mass over this time)
  • is determined to be healthy through completion of a health history questionnaire

Exclusion Criteria:

  • Are currently diagnosed or being treated for any cardiac, respiratory, endocrine, psychiatric, musculoskeletal, - renal, hepatic, neuromuscular or metabolic disease or disorder that in the judgement of the study participant's personal physician or research nurse that will preclude their safe participation or will contraindicate quality control over the collected data
  • are currently diagnosed with or are being treated for celiac disease, lactose intolerance, digestive insufficiencies or other gastrointestinal complications such as irritable bowel syndrome, ulcerative colitis, etc.
  • report having used anabolic steroids within the past 30 days
  • report have used any illicit or recreational drugs within the past 30 days
  • report the intake of any prescription or over-the-counter medications (i.e., antibiotics) that may impact study outcomes
  • report the current use of any dietary supplements known to impact digestion or sleep quality for the past 30 days
  • report already taking a probiotic within the past 30 days
  • have been actively trying to lose weight
  • are currently following a ketogenic or low carbohydrate diet within the past 30 days

Sites / Locations

  • Lindenwood University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Active Probiotic

Placebo

Arm Description

A mixture of probiotic strains (2.5 gram daily doses of 4 x 109 CFU/packet) of the following species (Lactobacillus fermentum, Lactobacillus rhamnosus, Lactobacillus plantarum, Bifidobacterium longum).

Maltodextrin capsule

Outcomes

Primary Outcome Measures

Beck Depression Index II
The Beck Depression Inventory (BDI) is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression. Total Score Levels of Depression 0-10 = These ups and downs are considered normal 11-16 = Mild mood disturbance 17-20 = Borderline clinical depression 21-30 = Moderate depression 31-40 = Severe depression over 40 = Extreme depression
COPE Inventory
The COPE Inventory is a multidimensional coping inventory to assess the different ways in which people respond to stress. Five scales (of four items each) measure conceptually distinct aspects of problem-focused coping (active coping, planning, suppression of competing activities, restraint coping, seeking of instrumental social support); five scales measure aspects of what might be viewed as emotion-focused coping (seeking of emotional social support, positive reinterpretation, acceptance, denial, turning to religion); and three scales measuring coping responses that arguably are less useful (focus on and venting of emotions, behavioral disengagement, mental disengagement).
Leiden Index of Depression Sensitivity - Revised
The Leiden Index of Depression Sensitivity (LEIDS) measures cognitive reactivity (CR) to sadness, an aspect of cognitive vulnerability to depression, conceptually similar to rumination. A higher total score on all the subscales except acceptance and coping shows higher CR.
Pittsburgh Sleep Quality Index
A self-rated questionnaire to assess sleep quality and disturbances 19 self-reported items Minimum score: 0; Maximum score: 21 Higher scoring indicated worse sleep quality
State-Trait Anxiety Inventory form Y1 and Y2
Measure of trait and state anxiety. All items on the scale are rated on a 4-point scale (e.g., from "Almost Never" to "Almost Always"). Higher scores indicate greater anxiety. The STAI is appropriate for those who have at least a sixth-grade reading level.
Behavioral Avoidance/Inhibition Scale
A measure of motivation to approach goal-oriented outcomes. Higher scores correspond to higher motivation to avoid goal oriented outcomes, lower scores indicate lower motivation to avoid goal-oriented outcomes.
Bowel Health Questionnaire
Measure of bowel health. Lower scores indicate lower number of GI disturbances and higher scores indicate higher number of GI disturbances

Secondary Outcome Measures

Hours Asleep
Total hours asleep each night as obtained through a fit bit activity monitor
Minutes Awake
Total minutes awake each night as obtained through a fit bit activity monitor
Number of awakenings
Number of times awakened each night as obtained through a FitBit activity monitor
Minutes of restlessness
Total minutes of restlessness each night as obtained through a FitBit activity monitor
Number of times Restless
Number of times restless each night as obtained through a FitBit activity monitor
Total time Awake and Restless
Total minutes of time awake and restless each night as obtained through a FitBit activity monitor
Total time in Bed
Total time in bed each night as obtained through a FitBit activity monitor
Calories Burned
Total KCal burned on average each day as obtained through a FitBit activity monitor
Steps
Total number of steps on average each day as obtained through a FitBit activity monitor
Distance
Total distance traveled each day on average each day as obtained through a FitBit activity monitor
Minutes Sedentary
Total minutes sedentary on average each day as obtained through a FitBit activity monitor
Minutes Lightly Active
Total minutes Lightly active on average each day as obtained through a FitBit activity monitor
Minutes Fairly Active
Total minutes Fairly active on average each day as obtained through a FitBit activity monitor
Minutes Very Active
Total minutes Very active on average each day as obtained through a FitBit activity monitor
Active Calories
Total minutes of active calories expended on average each day as obtained through a FitBit activity monitor
Body Composition
DEXA derived fat mass and fat free mass and bodyfat percentage

Full Information

First Posted
March 29, 2022
Last Updated
April 20, 2022
Sponsor
Lindenwood University
Collaborators
Increnovo, LLC
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1. Study Identification

Unique Protocol Identification Number
NCT05343533
Brief Title
Probiotic Administration on Mood
Acronym
PAM
Official Title
Impact of Probiotic Administration on Mood, Psychological Traits, Physical Activity, Stress, and Sleep Quality
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
July 17, 2019 (Actual)
Primary Completion Date
January 1, 2022 (Actual)
Study Completion Date
January 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lindenwood University
Collaborators
Increnovo, LLC

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
Researchers are looking to examine the impact of probiotic administration on symptoms commonly associated with depression, anxiety, stress, sleep quality, and associated emotional responses in healthy men and women.
Detailed Description
In recent years, the presence and awareness of a connection between the intestines and the brain has expanded leading to the understanding of developed communication pathways between the nervous, endocrine, and immune systems. Intestinal bacterial flora are active contributors to this axis through cellular signaling pathways and the release of immune system components, which fundamentally impact the function and action of various physiological systems. Interest in this area evolved through the understanding that various microbiota can produce neuroactive substances and neurotransmitters involved with the endocrine and autonomic nervous system pathways. This research has expanded to state that various bacterial products can influence cognitive functions, involving types of memory and problem-solving. Recent findings have begun to report on the impact that probiotic administration may have on mood, anxiety, and depression. Finally, recent work by Marotta et al. provided some of the first preliminary evidence that probiotic use may also impact mood and sleep quality. While initial work has developed this foundation, very little controlled research is available to help understand key contributing factors. For example, many key questions remain that future research should address to help better understand any impact probiotics may have on mood, depression, and anxiety. Some of these questions include: Do all forms (genus, strain, etc.) of probiotics exert these impacts? How quickly do they exert impact? How large is the impact? Are certain aspect of affect more impacted than others? Once supplemented, how long is the residual impact (if there is any)? To help provided more guidance towards some of these basic research questions, this study is being proposed. The purpose of the study is to expand upon the previous work of Marotta et al. and determine the impact of probiotic administration on mood, depressive symptoms, anxiety, sleep quality, and other personality traits in a larger group of healthy men and women. This study will expand on the supplementation regimen and include a wider variety of hormonal assessments than what has previously been completed using this combination of probiotics.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Sleep, Stress, Anxiety, Mood Disorders

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
andomized, double-blind, placebo-controlled, parallel study design that will evaluate the ability of a probiotic to influence mood, depressive symptoms, anxiety, sleep quality, and other personality traits in a group of healthy men and women
Masking
ParticipantInvestigator
Masking Description
All supplements were blinded from participant and investigator by a third party
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active Probiotic
Arm Type
Experimental
Arm Description
A mixture of probiotic strains (2.5 gram daily doses of 4 x 109 CFU/packet) of the following species (Lactobacillus fermentum, Lactobacillus rhamnosus, Lactobacillus plantarum, Bifidobacterium longum).
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Maltodextrin capsule
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic
Intervention Description
After baseline or initial testing, participants will be randomly assigned in a double-blind fashion to ingest on a daily basis for 6 weeks either a placebo or a probiotic supplement. Identical follow-up measurements will then occur each visit after taking their assigned supplement. After 6 weeks of administration, the supplementation protocol will stop and a final evaluation will be completed 3 weeks later (9 weeks after initial administration) to assess any residual impact of the assigned supplement after a 3-week washout.
Primary Outcome Measure Information:
Title
Beck Depression Index II
Description
The Beck Depression Inventory (BDI) is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression. Total Score Levels of Depression 0-10 = These ups and downs are considered normal 11-16 = Mild mood disturbance 17-20 = Borderline clinical depression 21-30 = Moderate depression 31-40 = Severe depression over 40 = Extreme depression
Time Frame
6 Weeks
Title
COPE Inventory
Description
The COPE Inventory is a multidimensional coping inventory to assess the different ways in which people respond to stress. Five scales (of four items each) measure conceptually distinct aspects of problem-focused coping (active coping, planning, suppression of competing activities, restraint coping, seeking of instrumental social support); five scales measure aspects of what might be viewed as emotion-focused coping (seeking of emotional social support, positive reinterpretation, acceptance, denial, turning to religion); and three scales measuring coping responses that arguably are less useful (focus on and venting of emotions, behavioral disengagement, mental disengagement).
Time Frame
6 weeks
Title
Leiden Index of Depression Sensitivity - Revised
Description
The Leiden Index of Depression Sensitivity (LEIDS) measures cognitive reactivity (CR) to sadness, an aspect of cognitive vulnerability to depression, conceptually similar to rumination. A higher total score on all the subscales except acceptance and coping shows higher CR.
Time Frame
6 weeks
Title
Pittsburgh Sleep Quality Index
Description
A self-rated questionnaire to assess sleep quality and disturbances 19 self-reported items Minimum score: 0; Maximum score: 21 Higher scoring indicated worse sleep quality
Time Frame
6 weeks
Title
State-Trait Anxiety Inventory form Y1 and Y2
Description
Measure of trait and state anxiety. All items on the scale are rated on a 4-point scale (e.g., from "Almost Never" to "Almost Always"). Higher scores indicate greater anxiety. The STAI is appropriate for those who have at least a sixth-grade reading level.
Time Frame
6 weeks
Title
Behavioral Avoidance/Inhibition Scale
Description
A measure of motivation to approach goal-oriented outcomes. Higher scores correspond to higher motivation to avoid goal oriented outcomes, lower scores indicate lower motivation to avoid goal-oriented outcomes.
Time Frame
6 weeks
Title
Bowel Health Questionnaire
Description
Measure of bowel health. Lower scores indicate lower number of GI disturbances and higher scores indicate higher number of GI disturbances
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Hours Asleep
Description
Total hours asleep each night as obtained through a fit bit activity monitor
Time Frame
6 weeks
Title
Minutes Awake
Description
Total minutes awake each night as obtained through a fit bit activity monitor
Time Frame
6 weeks
Title
Number of awakenings
Description
Number of times awakened each night as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Minutes of restlessness
Description
Total minutes of restlessness each night as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Number of times Restless
Description
Number of times restless each night as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Total time Awake and Restless
Description
Total minutes of time awake and restless each night as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Total time in Bed
Description
Total time in bed each night as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Calories Burned
Description
Total KCal burned on average each day as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Steps
Description
Total number of steps on average each day as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Distance
Description
Total distance traveled each day on average each day as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Minutes Sedentary
Description
Total minutes sedentary on average each day as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Minutes Lightly Active
Description
Total minutes Lightly active on average each day as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Minutes Fairly Active
Description
Total minutes Fairly active on average each day as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Minutes Very Active
Description
Total minutes Very active on average each day as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Active Calories
Description
Total minutes of active calories expended on average each day as obtained through a FitBit activity monitor
Time Frame
6 weeks
Title
Body Composition
Description
DEXA derived fat mass and fat free mass and bodyfat percentage
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: between the ages of 18 - 50 years has a body mass index between 18.5 - 30 kg/m2. Anyone with a body mass index between 30 - 32 kg/m2, but has a body composition <25% fat -for men and <35% for women will be accepted into the study has been weight stable for the past three months (defined as less than a 5% variation in body -mass over this time) is determined to be healthy through completion of a health history questionnaire Exclusion Criteria: Are currently diagnosed or being treated for any cardiac, respiratory, endocrine, psychiatric, musculoskeletal, - renal, hepatic, neuromuscular or metabolic disease or disorder that in the judgement of the study participant's personal physician or research nurse that will preclude their safe participation or will contraindicate quality control over the collected data are currently diagnosed with or are being treated for celiac disease, lactose intolerance, digestive insufficiencies or other gastrointestinal complications such as irritable bowel syndrome, ulcerative colitis, etc. report having used anabolic steroids within the past 30 days report have used any illicit or recreational drugs within the past 30 days report the intake of any prescription or over-the-counter medications (i.e., antibiotics) that may impact study outcomes report the current use of any dietary supplements known to impact digestion or sleep quality for the past 30 days report already taking a probiotic within the past 30 days have been actively trying to lose weight are currently following a ketogenic or low carbohydrate diet within the past 30 days
Facility Information:
Facility Name
Lindenwood University
City
Saint Charles
State/Province
Missouri
ZIP/Postal Code
63301
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Probiotic Administration on Mood

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