Probiotic Intervention for Acute Stress

Probi AB

Status: Completed

Conditions: Stress

Treatments: Dietary Supplement: Probiotic supplement; Dietary Supplement: Placebo supplement

Study type: Interventional

Funder types: Industry

Identifiers

NCT03284905

SP17

Details and patient eligibility

About

Efficacy of probiotics on acute stress

Enrollment: 70 patients

Sex: All

Ages: 19 to 35 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 19-35 years
• SMBQ-score ≥3.75
• Understand Swedish in spoken and written terms
• Willing and able to give written informed consent for participating in the study
• Intake of probiotics within two weeks prior to the start of the study

Exclusion criteria

• BMI> 30
• Pregnant
• Antibiotic treatment in the last three months
• Known disease (diabetes, pulmonary or cardiovascular disease, celiac disease, thyroid problems, gastrointestinal disease) or mental illness
• Use of psychotropic drugs, beta blockers, asthma or rheumatoid arthritis drugs, steroid drugs or local steroid treatment

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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70 participants in 2 patient groups, including a placebo group

Probiotics

Active Comparator group

Treatment:

Dietary Supplement: Probiotic supplement

Placebo

Placebo Comparator group

Treatment:

Dietary Supplement: Placebo supplement