The effect of probiotic consumption on fatigue and sexual function in postmenopausal women

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180707040370N11

Enrollment

Registered

2024-08-16

Start date

2024-09-05

Completion date

Unknown

Last updated

2024-08-26

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

Conditions

fatigue severity and sexual function in postmenopausal women. Menopausal and female climacteric states

Interventions

Intervention 1: Intervention group: Probiotic supplement will be prescribed in the form of Oral Capsule 200 mg, Once a day for 6 weeks. Including Lactobacillus casei, Lactobacillus acidophilus, Lactob

Eligibility

Sex/Gender

Female

Age

45 Years to 55 Years

Inclusion criteria

Inclusion criteria: age between 45-55 not using cigarette or alcohol not having physical or mental diseases not using of relaxation techniques not using of hormonal or herbal therapies at least 1 to 5 years have passed since menopause

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Fatigue severity. Timepoint: Before the intervention, 3 and 6 weeks after the intervention. Method of measurement: Fatigue Severity Scale (?FFS).;Sexual function. Timepoint: Before the intervention, 3 and 6 weeks after the intervention. Method of measurement: Female Sexual Function Index.	—

Secondary

Measure	Time frame
Menopausal quality of life. Timepoint: Before the intervention, 3 and 6 weeks after the intervention. Method of measurement: Menopause-Specific Quality of Life (MENQOL).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEnsiyeh Jenabi

Hamedan University of Medical Sciences

en.jenabi@yahoo.com+98 81 3838 1938

Outcome results

None listed

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