Sexual function and sexual dysfunction. Sexual dysfunction not due to a substance or known physiological condition
Conditions
Interventions
Intervention 1: Intervention group: This group includes 38 people who will use an applicator of 5% case leaf vaginal gel, 15 minutes before sexual intercourse for 4 weeks. Intervention 2: Control grou
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: A married woman of reproductive age (18-40) years old Having informed consent to participate in the research Having a sexual function score based on the FSFI questionnaire is less than 28 Has a history of NVD Having sex at least once a week A resident of Mashhad or the suburbs Having at least reading and writing literacy Having a regular period cycle (26-32 days) and not having AUB Having a depression score of less than 21, anxiety less than 15, and stress less than 26 in the DASS questionnaire
Exclusion criteria
Exclusion criteria: Allergy to herbal substances or herbs pregnancy and breastfeeding infertility hormone therapy or use of sex hormones 2 months before the study Specific mental illness in couples and specific medical illness affecting sexual function in women and husbands vaginal atrophy Pelvic radiation therapy or chemotherapy to treat cancer oophorectomy early menopause uncontrolled diabetes Treatment with drugs used to reduce estrogen levels in women with endometriosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual function score in the FSFI questionnaire. Timepoint: Measurement of sexual function at the beginning of the study (before the start of the intervention) and 4 weeks after using the vaginal gel. Method of measurement: Female Sexual Function Index Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactraheleh babazadeh
Mashhad University of Medical Sciences
Outcome results
None listed