endometriosis.
Conditions
Interventions
Intervention 1: Intervention group: In 50 women with endometriosis under medical treatment in the intervention group, an educational application will be installed on the mobile phone and will be avail
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Endometriosis has been diagnosed in them by a gynecologist through ultrasound To be sexually active during the last month There is no known infertility problem in any of the couples There should be no known sexual dysfunction in the male partner such as erectile dysfunction, ejaculation disorder Does not have any known underlying diseases such as mental illness, cardiovascular disease, kidney disease, diabetes, excretory disease, pelvic inflammatory disease and other women's diseases Absence of urinary tract infection, vaginitis, cervical inflammation, active wounds or genital lesions that interfere with sexual intercourse, or a history of sexual assault Women have not used any drugs affecting sexual function such as antidepressants, beta blockers, antihistamines, antipsychotics, benzodiazepines, antiepileptic drugs Couples should not consume cigarettes, alcohol and drugs Not experiencing stressful events (death of a child or a close relative, severe illness of a close relative, imprisonment of a family member, depression, etc.) in the last 3 months The couple has not taken various sex education classes or courses
Exclusion criteria
Exclusion criteria: Failure to fully complete research questionnaires
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Female sexual function. Timepoint: Before starting the intervention. Method of measurement: female sexual performance questionnaire.;Female sexual quality of life. Timepoint: Before starting the intervention. Method of measurement: Questionnaire of the quality of women's sexual life. | — |
Secondary
| Measure | Time frame |
|---|---|
| Female sexual function. Timepoint: One month and two months after the intervention. Method of measurement: female sexual function questioner.;Female sexual quality of life. Timepoint: One month and two months after the intervention. Method of measurement: female sexual quality of life questioner. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactmobina khorrami
Shahid Beheshti University of Medical Sciences
Outcome results
None listed