Investigating the effect of paraprobiotics in stress treatment
Not Applicable
- Conditions
- ?Stress during the final exam.
- Registration Number
- IRCT20240128060833N1
- Lead Sponsor
- Malayer university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
student
20-30 yearss old
Exclusion Criteria
use of psychoactive drugs
food allergy
mental problems under treatment
using probiotics
using probiotic products
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Salivary cortisol. Timepoint: At the beginning of the study, after 5 and10 weeks after the start of drinking. Method of measurement: cortisol kit.
- Secondary Outcome Measures
Name Time Method Sleep quality, general health, sleep latency. Timepoint: At the beginning of the study and 5 and 10 weeks after the start of drinking. Method of measurement: 28-question general health questionnaires, self-report depression and sleep quality, Pittsburgh sleep quality index, which measures sleep quality and insomnia.