- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03935061
Effects of Mulberry Juice on Inflammatory Status and Clinical Symptoms in Patients With General Anxiety Disorder
September 9, 2019 updated by: Taipei Medical University
Auxiliary Effects of Mulberry Juice on Inflammatory Status and Clinical Symptoms in Patients With General Anxiety Disorder: A Single-Blinded Trial
Anxiety and depression are normally associated with inflammation reactions and interleukin (IL) related pathways are most evidently involved.
IL-17A (interleukin 17A) induces psoriasis-like inflammation and depression-like behaviors in animals and can be relieved by using IL-17A antibody.
Also, human association studies found that IL-17A and certain downstream ILs are associated with the severity of anxiety.
IL-17A is a sentinel cytokine.
On binding with interleukin 17A receptor (IL-17RA) and interleukin 17C receptor (IL-27RC), it induces signaling cascades via nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB), P38 mitogen-activated protein kinases (p38MAPK) and CCAAT-enhancer-binding proteins (C/EBPs) knots, and stimulates subsequent cell secretions of cytokines and chemokines.
Cyanidin 3-O-glucoside, the main anthocyanin component of mulberry, competes with IL-17A to bind its receptors and inhibits subsequent downstream cascades.
The investigators plan to use a single-blinded randomized controlled trial to evaluate the auxiliary effect of mulberry juice in general anxiety disorder, including differences in psychiatric symptoms and levels of IL-related markers between the experimental and control groups, and contribution of IL-related genes in the auxiliary effect.
Study Overview
Status
Unknown
Intervention / Treatment
Detailed Description
The etiology, pathogenesis, and pathophysiology of psychiatric disorders are not limited to the brain.
Anxiety and depression are normally associated with inflammation reactions and interleukin (IL) related pathways are most evidently involved.
Previous animal studies showed that administration of IL-17A induces psoriasis-like inflammation and depression-like behavior, and can be relieved by using IL-17A antibody, while in humans, association studies showed that serum IL-17A and certain downstream ILs are associated with the severity of anxiety.
Also, the result of human genetic studies also identified several IL genes associated with anxiety and depression.
IL-17A is a sentinel cytokine.
On binding with interleukin 17A receptor (IL-17RA) and interleukin 17C receptor (IL-27RC), it induces signaling cascades via nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB), P38 mitogen-activated protein kinases (p38MAPK) and CCAAT-enhancer-binding proteins (C/EBPs) knots, and stimulates subsequent cell secretions of cytokines and chemokines.
Many studies have demonstrated that consumption of proanthocyanidin-rich or anthocyanin-rich berries, berries juice or other secondary products reduce a variety of inflammation symptoms in humans.
However, these berries do not meet a low-cost requirement for general nutritional recommendation and new drug development in Taiwan due to the additional import cost.
On the other hand, cyanidin 3-O-glucoside, the main anthocyanin component of local mulberry, competes with IL-17A to bind its receptors and inhibits subsequent downstream cascades.
Without interfering the on-going treatment of the patients, this proposal plans to use a single-blinded randomized controlled trial to evaluate the auxiliary effect of mulberry juice in general anxiety disorder, including differences in psychiatric symptoms (anxiety, depression, and functions) and levels of IL-related markers between the experimental and control groups, and contribution of IL-related genes in the auxiliary effect.
Study Type
Interventional
Enrollment (Anticipated)
104
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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New Taipei City, Taiwan, 235
- Recruiting
- Taipei Medical University Shuang Ho Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
• meet the criteria for GAD in the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition, as their primary diagnosis
Exclusion Criteria:
- severe physical diseases that required intensive care or additional medical attention such as terminal cancer, stroke, and end-stage renal disease
- psychotic symptoms or recent suicide attempts
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: Mulberry juice
Two bottles (600 ml/bottle) of sanitized mulberry juice are delivered to the patients of the experimental group 20 days before the next clinic visit, with instruction to consume 50 ml of juice diluted with drinking water at room temperature.
A reminder of the next clinic visit for continuous treatment is attached.
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On the second visit at the 1st month, measurements of clinical symptoms and inflammation status are conducted.
No mulberry juice is given to patients further on.
All patients are evaluated again with the same assessment tools, as well as the immunology markers in their sera during the third visit.
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NO_INTERVENTION: Controlled
Patients of the controlled group are informed of their allocation results along with a reminder of the next clinic visit.
On the second visit at the 1st month, measurements of clinical symptoms and inflammation status are conducted.
No mulberry juice is given to patients further on.
All patients are evaluated again with the same assessment tools, as well as the immunology markers in their sera during the third visit.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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General Anxiety Disorder-7 items (GAD-7)
Time Frame: 5 to 10 minutes
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GAD-7 measures anxiety status.
The questionnaire is self-reported.
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5 to 10 minutes
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Patient Health Questionnaire-9 items (PHQ-9)
Time Frame: 5 to 10 minutes
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PHQ-9 measure depression status.
This questionnaire is self-reported.
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5 to 10 minutes
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World Health Organization Quality of Life - Brief (WHOQOL-BREF)
Time Frame: 5 to 10 minutes
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WHOQOL-BREF measures the quality of life.
The questionnaire is self-reported.
|
5 to 10 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inflammation markers
Time Frame: 6 months
|
Inflammation status of the patients are evaluated by measuring CRP, known cytokines (Interleukin- 6 [IL-6], Interleukin-1β [IL-1β], tumor necrosis factor-α (TNF-α), granulocyte colony-stimulating factor [G-CSF], granulocyte-macrophage colony-stimulating factor [GM-CSF], and transforming growth factor [TGF-β]), chemokines (IL-8, GRO-α, and MCP-1), and PGE in sera, in addition to the sentinel molecule IL-17A.
All markers are measured by using ELISA assays according to manufacturer instructions.
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6 months
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Inflammation genes
Time Frame: 24 months
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Inflammation genes including CRP, cytokines (IL-6, IL-1β, TNF-α, G-CSF, GM-CSF, and TGF-β), chemokines (IL-8, GRO-α, and MCP-1), and PGE in addition to IL-17A, are to be genotyped.
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24 months
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
July 3, 2019
Primary Completion (ANTICIPATED)
June 30, 2020
Study Completion (ANTICIPATED)
May 31, 2021
Study Registration Dates
First Submitted
April 26, 2019
First Submitted That Met QC Criteria
April 30, 2019
First Posted (ACTUAL)
May 2, 2019
Study Record Updates
Last Update Posted (ACTUAL)
September 11, 2019
Last Update Submitted That Met QC Criteria
September 9, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- N201802079
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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