Skip to main content
OpenTrials
Completed

NCT Number: NCT05343533

Probiotic Administration on Mood

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Lindenwood University

Saint Charles, Missouri, 63301, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Probiotic

Dietary Supplement

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 outcomes

  1. Beck Depression Index II

    Time frame: 6 Weeks

    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

  2. COPE Inventory

    Time frame: 6 weeks

    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).

  3. Leiden Index of Depression Sensitivity - Revised

    Time frame: 6 weeks

    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.

  4. Pittsburgh Sleep Quality Index

    Time frame: 6 weeks

    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

  5. State-Trait Anxiety Inventory form Y1 and Y2

    Time frame: 6 weeks

    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.

  6. Behavioral Avoidance/Inhibition Scale

    Time frame: 6 weeks

    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.

  7. Bowel Health Questionnaire

    Time frame: 6 weeks

    Measure of bowel health. Lower scores indicate lower number of GI disturbances and higher scores indicate higher number of GI disturbances

Secondary outcomes

  1. Hours Asleep

    Time frame: 6 weeks

    Total hours asleep each night as obtained through a fit bit activity monitor

  2. Minutes Awake

    Time frame: 6 weeks

    Total minutes awake each night as obtained through a fit bit activity monitor

  3. Number of awakenings

    Time frame: 6 weeks

    Number of times awakened each night as obtained through a FitBit activity monitor

  4. Minutes of restlessness

    Time frame: 6 weeks

    Total minutes of restlessness each night as obtained through a FitBit activity monitor

  5. Number of times Restless

    Time frame: 6 weeks

    Number of times restless each night as obtained through a FitBit activity monitor

  6. Total time Awake and Restless

    Time frame: 6 weeks

    Total minutes of time awake and restless each night as obtained through a FitBit activity monitor

  7. Total time in Bed

    Time frame: 6 weeks

    Total time in bed each night as obtained through a FitBit activity monitor

  8. Calories Burned

    Time frame: 6 weeks

    Total KCal burned on average each day as obtained through a FitBit activity monitor

  9. Steps

    Time frame: 6 weeks

    Total number of steps on average each day as obtained through a FitBit activity monitor

  10. Distance

    Time frame: 6 weeks

    Total distance traveled each day on average each day as obtained through a FitBit activity monitor

  11. Minutes Sedentary

    Time frame: 6 weeks

    Total minutes sedentary on average each day as obtained through a FitBit activity monitor

  12. Minutes Lightly Active

    Time frame: 6 weeks

    Total minutes Lightly active on average each day as obtained through a FitBit activity monitor

  13. Minutes Fairly Active

    Time frame: 6 weeks

    Total minutes Fairly active on average each day as obtained through a FitBit activity monitor

  14. Minutes Very Active

    Time frame: 6 weeks

    Total minutes Very active on average each day as obtained through a FitBit activity monitor

  15. Active Calories

    Time frame: 6 weeks

    Total minutes of active calories expended on average each day as obtained through a FitBit activity monitor

  16. Body Composition

    Time frame: 6 weeks

    DEXA derived fat mass and fat free mass and bodyfat percentage

Sponsors and collaborators

Lead sponsor

Lindenwood University

Other

Collaborators

  • Increnovo LLC

Registry information

Official study title

Impact of Probiotic Administration on Mood, Psychological Traits, Physical Activity, Stress, and Sleep Quality

Acronym: PAM

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Apr 25, 2022
Registry last updated
Apr 25, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.