Design and evaluation the effect of Educational mobile Application on sexual function and sexual quality of life in women with endometriosis under medical treatment
- Conditions
- endometriosis.
- Registration Number
- IRCT20230820059202N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 100
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
Failure to fully complete research questionnaires
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.