?????? ?????? ????. Sexual dysfunction not due to a substance or known physiological condition
Conditions
Interventions
Intervention 1: The intervention group is menopausal women, which will be divided into two groups: oral cinnamon capsules (400 mg) and vitex-agnus capsules (400 mg). The capsules will be provided at
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
45 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Be Iranian. 2. Have at least literacy. 3. Do not have speech, hearing or mental disorders that prevent communication with the researcher. 4. It's been at least a year since they stopped menstruating. 5. Have a married life with her spouse. 6. There is no inclination or obligation to use hormone replacement therapy. 7. As menopausal woman sated, do not use any chemical or herbal remedies to treat her problem. 8. Have sexual activity. 9. A postmenopausal wife does not have a sexual problem. 10. They have not undergone hysterectomy and ovariectomy, cystocele, rectocele, and mastectomy. 11. Menopausal women and their spouses do not have a known mental illness. 12. Not addicted to cigarettes or drugs. 13. He has not recently used antidepressants drugs. 14. Have no history of known chronic diseases such as high blood pressure, diabetes, asthma, weaken the immune system, etc. 15. Has no history of allergy to medicinal plants. 16. Do not use herbal teas during medication. 17. Age between 45 and 65 years
Exclusion criteria
Exclusion criteria: 1. Possible sensitivity to capsules 2. Do not take the capsule for a week or more 3. Lack of desire to continue treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual dysfunction according to the FSFI questionnaire. Timepoint: Before intervention, 2 month after intervention, 3 month after intervention. Method of measurement: FSFI questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sexual desire. Timepoint: Before intervention, 2 month after intervention, 3 moth after intervention. Method of measurement: The Female Sexual Function Index (FSFI) questionnaire.;Sexual satisfaction. Timepoint: Before intervention, 2 month after intervention, 3 month after intervention. Method of measurement: The Female Sexual Function Index (FSFI) questionnaire.;Orgasm. Timepoint: Before intervention, 2 month after intervention, 3 month after intervention. Method of measurement: The Female Sexual Function Index (FSFI) questionnaire.;Arousal. Timepoint: Before intervention, 2 month after intervention, 3 month after intervention. Method of measurement: The Female Sexual Function Index (FSFI) questionnaire.;Lubrication. Timepoint: Before intervention, 2 month after intervention, 3 month after intervention. Method of measurement: The Female Sexual Function Index (FSFI) questionnaire.;Pain during intercourse. Timepoint: Before intervention, 2 month after intervention, 3 month after intervention. Method of measurement: The Female Sexual Function Index (FSFI) questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactTanya Koliji
Shahid Beheshti University of Medical Sciences
Outcome results
None listed