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Nutritional Trial With Probiotic Fortified Milk in Women Affected by Insomnia (Prosit)

Primary Purpose

Sleep Disorders

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Fortified milk
Placebo milk
Sponsored by
University of Bologna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Disorders focused on measuring golden milk, insomnia, gut-brain axis

Eligibility Criteria

55 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Subjects with an age between 55 and 70 years old, only females, free-living, affected by chronic insomnia defined according to the criteria of the International Classification of Sleep Disorders (2014).

Exclusion Criteria:

  • Allergy or intolerance to cow's milk. Use of Benzodiazepines, "Z drugs" or anti-depressive drugs during the three months preceding the start of the trial. Celiac disease and other intestinal malabsorption or inflammatory bowel diseases (Crohn's disease and ulcerative colitis). Chronic therapy with anticoagulant, corticosteroid, anticancer drugs and immunosuppressants. Diabetes type I and type II, chronic viral hepatitis, neurological disorders or dementia, cancer, poor prognosis disease in the short term. Use of anti-inflammatory drugs or inflammatory-infective events within 7 days before the start of the trial and use of antibiotics or vaccinations within 30 days before.

Sites / Locations

  • University of Bologna-Department of Speciality, Diagnostic and Experimental Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Fortified milk

Placebo milk

Arm Description

The subjects assumed daily 250 ml of fortified milk for 12 weeks.

The subjects assumed daily 250 ml of placebo milk for 12 weeks.

Outcomes

Primary Outcome Measures

Self reported quality of sleep
Sleep quality assessed by questionnaires
Measured quality of sleep
assessed by actigraph

Secondary Outcome Measures

Levels of stress
Stress was evaluated by PSS questionnaire and 24-h urinary cortisol levels
Inflammatory status
Dosage in plasma of the following cytokines: IL-1β, IL-4, IL-6, IL-10, IL-17A, IL-17F, IL-21, IL-22, IL-23, IL-25, IL-31, IL-33, IFN-γ, sCD40L, TNF-α, IL-17 A/F by Elisa immunoassay.
Evalution of glycomics
Plasmatic N-glycans by capillary electrophoresis (DSA-FACE).
Levels of anxiety
Stress was evaluated by STAI-Y2
Levels of depression.
Stress was evaluated by BDI-II questionnaire
Evalution of epigenetic
Epigenetic analysis of ELOVL2, FHL2, PENK genes by "Sequenom"
Gut Microbiota composition
Analysis of gut-microbiota composition by 454 Pyrosequencing of the V4 region of the 16S rRNA gene.

Full Information

First Posted
July 22, 2016
Last Updated
June 12, 2019
Sponsor
University of Bologna
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1. Study Identification

Unique Protocol Identification Number
NCT03985228
Brief Title
Nutritional Trial With Probiotic Fortified Milk in Women Affected by Insomnia
Acronym
Prosit
Official Title
Promotion of Consumer's Health: Nutritional Enhancement/Valorization of Agrofood Italian Traditional Products (PROS.IT)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
November 20, 2015 (undefined)
Primary Completion Date
July 2016 (Actual)
Study Completion Date
August 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Bologna

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study "Nutritional Trial With Probiotic Fortified Milk in Women Affected by Insomnia" is a part of a complex and multi-sectoral development research project (PROS.IT) with the participation of University Research Institutes and small/medium Italian enterprises. The general objective of the Project is to promote the collaboration between the best scientific research, both epidemiological and experimental, and the most advanced technologies to develop fortified foods that meeting the specific nutritional requirements of adult consumers. This objective will be achieved by the nutritional improvement of primary production, the development of innovative functional foods at high added value, in addition to traditional products functionalized, which are peculiar of the Italian local districts.
Detailed Description
Sleep disorders and, in particular, insomnia, are quite common conditions in over 55 population, especially among women. Insomnia becomes a chronic pathology when the difficulty in initiating or maintaining sleep occurs more times a week for several months and is associated to a constant feeling of fatigue, concentration problems, mood disorders and social and family troubles severely impairing the quality of life. In according to the sleep hygiene guidelines, the therapeutic treatments for insomnia include drugs (benzodiazepines, non-benzodiazepines, antidepressants) with often not fully satisfactory results for the patient and entailing a series of side effects, such as daytime sleepiness, lack of attention and energy in addition to mental confusion. Recently, some researches in neurological field have shown that disorders affecting central nervous system, as well as sleep and circadian rhythm disruption, can be associated to specific alteration of the gut microbiota. The enteric nervous system has been referred to as a "second brain" able to interact with the central nervous system impinging upon higher cognitive functions through a bidirectional communication system known as gut-brain axis. The gut microflora plays a crucial role in gut-brain axis, modulating stress response through the Hypothalamic-Pituitary-Adrenal axis and thus influencing memory, mood, cognition and sleep architecture. Therefore, a non-pharmacological intervention aimed to improve gut microbiota and the inflammatory bowel conditions could be an effective strategy to counteract insomnia. In the framework of Pros.IT project, the Granarolo S.p.A. in collaboration with the University of Bologna has developed a milk enriched with different micronutrients (vitamins, ω-3 fatty acids, prebiotics, curcumin) and "infant-type" probiotics isolated from human milk and endowed with immunomodulating activity. This supplementation should improve the overall health status, and in particular the plant extracts, prebiotics and probiotics with anti-inflammatory and immunomodulatory activities should ameliorate significantly sleep quality and stress perception through the modulation of gut microbiota and gut-brain axis. The main goal of this study is to evaluate the effect of the administration of a functional milk reinforced with probiotics (250ml/die), vitamins and other micronutrients on sleep of patients suffering from chronic insomnia. An objective assessment it requires a value at least higher than 3% of increase of the sleep efficiency, since the 3% is the percentage of improvement recognized to the common drugs against insomnia. The study is randomized, double-blind, placebo-controlled trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Disorders
Keywords
golden milk, insomnia, gut-brain axis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
38 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fortified milk
Arm Type
Experimental
Arm Description
The subjects assumed daily 250 ml of fortified milk for 12 weeks.
Arm Title
Placebo milk
Arm Type
Placebo Comparator
Arm Description
The subjects assumed daily 250 ml of placebo milk for 12 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Fortified milk
Other Intervention Name(s)
golden milk
Intervention Description
Ultra high temperature UHT, partly-skimmed milk (1% fat), highly digestible (lactose <0.01%), enriched in whey protein (5%) and calcium (0.24%), supplemented with unsaturated fatty acids omega-3 (DHA + EPA), vitamins (D, B12, B6, B9, E, C), prebiotics (FOS) and phyto curcuminoids (sunflower lecithin). Milk had to be associated with a packet of lyophilized and concentrated probiotics (Bifidobacteria infant-type and / or Lactobacilli), at the time of consumption. Milk and probiotics had been produced or supplied by Granarolo s.p.a.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo milk
Intervention Description
Ultra high temperature UHT, partly-skimmed milk (1% fat), highly digestible (lactose <0.01%) with standard proteins of milk (3.1%) and color additive "quantum satis". Milk had to be associated with a packet of maltodextrin "Food Grade", at the time of consumption. Milk and maltodextrin had been produced or supplied by Granarolo s.p.a.
Primary Outcome Measure Information:
Title
Self reported quality of sleep
Description
Sleep quality assessed by questionnaires
Time Frame
Change from baseline Sleep evaluation at 12 weeks milk intake
Title
Measured quality of sleep
Description
assessed by actigraph
Time Frame
Change from baseline Sleep evaluation at 12 weeks milk intake
Secondary Outcome Measure Information:
Title
Levels of stress
Description
Stress was evaluated by PSS questionnaire and 24-h urinary cortisol levels
Time Frame
12 weeks
Title
Inflammatory status
Description
Dosage in plasma of the following cytokines: IL-1β, IL-4, IL-6, IL-10, IL-17A, IL-17F, IL-21, IL-22, IL-23, IL-25, IL-31, IL-33, IFN-γ, sCD40L, TNF-α, IL-17 A/F by Elisa immunoassay.
Time Frame
12 weeks
Title
Evalution of glycomics
Description
Plasmatic N-glycans by capillary electrophoresis (DSA-FACE).
Time Frame
12 weeks
Title
Levels of anxiety
Description
Stress was evaluated by STAI-Y2
Time Frame
12 weeks
Title
Levels of depression.
Description
Stress was evaluated by BDI-II questionnaire
Time Frame
12 weeks
Title
Evalution of epigenetic
Description
Epigenetic analysis of ELOVL2, FHL2, PENK genes by "Sequenom"
Time Frame
12 weeks
Title
Gut Microbiota composition
Description
Analysis of gut-microbiota composition by 454 Pyrosequencing of the V4 region of the 16S rRNA gene.
Time Frame
12 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects with an age between 55 and 70 years old, only females, free-living, affected by chronic insomnia defined according to the criteria of the International Classification of Sleep Disorders (2014). Exclusion Criteria: Allergy or intolerance to cow's milk. Use of Benzodiazepines, "Z drugs" or anti-depressive drugs during the three months preceding the start of the trial. Celiac disease and other intestinal malabsorption or inflammatory bowel diseases (Crohn's disease and ulcerative colitis). Chronic therapy with anticoagulant, corticosteroid, anticancer drugs and immunosuppressants. Diabetes type I and type II, chronic viral hepatitis, neurological disorders or dementia, cancer, poor prognosis disease in the short term. Use of anti-inflammatory drugs or inflammatory-infective events within 7 days before the start of the trial and use of antibiotics or vaccinations within 30 days before.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudio Franceschi, MD
Organizational Affiliation
University of Bologna
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Bologna-Department of Speciality, Diagnostic and Experimental Medicine
City
Bologna
ZIP/Postal Code
40126
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No

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Nutritional Trial With Probiotic Fortified Milk in Women Affected by Insomnia

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