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The effect of Synbiotic on aggression

The effect of Synbiotic supplementation on the severity of different types of self-reported aggression and anger in healthy adult men.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20091114002709N53
Enrollment
100
Registered
2020-02-22
Start date
2021-09-23
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: aggression. Condition 2: anger.

Interventions

Intervention 1: Intervention group: intake of two daily synbiotic of Familact capsule (produced by Bio-Fermentation Company) for 2 months, each capsule being 500 mg containing 7 species of Lactobacill

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Willingness to cooperate 18 to 75 years old Having physical health and no history of cardiovascular, gastrointestinal, metabolic, autoimmune disease, allergies, etc. No history of mental disease such as epilepsy, Bulimia nervosa, Anorexia, etc. No anti-depressant, anti-inflammatory, anti-obesity, anti-diabetic medications, and hormone therapy for at least two months ago. Not taking any omega-3, multivitamin-mineral supplements for at least two months ago. lack of severe family conflicts in 3 months ago.

Exclusion criteria

Exclusion criteria: The dissatisfaction to continue cooperation. Probiotic-containing foods consumption two weeks before and during the study. Antibiotic consumption during the study. Severe family conflicts during the study. consuming Less than 80% of supplements delivered to adolescents. Incidence of any disease during the study.

Design outcomes

Primary

MeasureTime frame
Anger from Aggression Questionnaire. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Aggression Questionnaire.

Secondary

MeasureTime frame
Aggression. Timepoint: Before the intervention and 2 months after the intervention. Method of measurement: Aggression Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Farzad Shidfar

Iran University of Medical Sciences

Shidfar.f@iums.ac.ir+98 21 8862 2755

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026