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Effects of probiotic in generalized anxiety disorder

Phase 2
Conditions
Generalized anxiety disorder.
Anxiety that is generalized and persistent but not restricted to, or even strongly predominating in, any particular environmental circumstances (i.e. it is free-floating). The dominant symptoms are variable but include complaints of persistent nervousne
Registration Number
IRCT201612072394N35
Lead Sponsor
Vice-chancellor for research, Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

DSM-V diagnosed of GAD; Adults between 18 and 65 years old; Willing to participate.
exclusion criteria: Having illness including liver disease and kidney disease, diabetes, immune deficiency, etc; Having psychological illnesses including psychosis, Suicidal ideation, bipolar disorder and major depression; People who are expected to have limited partnerships such as forgetfulness and pregnancy; Taking any medication in the previous 1 month; Taking any medication related to psychiatric diseases including antidepressants, antipsychotics, etc. (maximum of two times per week) and antibiotics in the previous 1 month; Taking any supplement including probiotic supplement, fiber, prebiotics, omega-3, vitamins and minerals in the previous 1 month; Consumption of fermented foods (except yogurt), such as sour cream, acidophilus milk, kefir and some cheeses such as blue vein cheese or Swiss cheese in the previous 1 month; substance abuse; The compliance less than 80%.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Symptom severity. Timepoint: at baseline, after 1 month and after 2 month. Method of measurement: Beck Anxiety Inventory, Hamilton Rating Scale for anxiety and State-Trait Anxiety Inventory questionnaires.;Plasma acth. Timepoint: at baseline, after 1 month and after 2 month. Method of measurement: Electro-chemiluminescence immunoassay.;Serum cortisol. Timepoint: at baseline, after 1 month and after 2 month. Method of measurement: Chemiluminescence immunoassay.;Quality of life. Timepoint: at baseline, after 1 month and after 2 month. Method of measurement: quality of life, world health organization questionnaire.
Secondary Outcome Measures
NameTimeMethod
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