Sexual function - Quality of sexual life. Other sexual dysfunction
Conditions
Interventions
Intervention 1: Intervention group: Auriculotherapy for Lactating primipara women eligible for study, for 10 sessions a week, 2 times for 5 weeks. Intervention 2: Control group: Auriculotherapy for
Sponsors
??Alborz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: single - term delivery Pass 6 weeks to 6 months of delivery The number of Edinburgh questionnaires (postpartum depression) is less than 13 18 to 45 years old Having a healthy eardrum for Auriculotherapy Exclusively breastfeeding
Exclusion criteria
Exclusion criteria: Pregnancy during study Loss of infant during study Being away from the spouse Hearing problems (tinnitus, ear infections, or otitis media). Having underlying physical illnesses (blood pressure, diabetes, and seizures in the participant or her spouse's)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Female sexual function. Timepoint: Before intervention, after intervention, one month after intervention. Method of measurement: MSISQ-19.;Women's sexual Quality of Life. Timepoint: Before intervention, after intervention, one month after intervention. Method of measurement: Women's Quality of Life Quality Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Mansoureh Yazdkhshati
Karaj University of Medical Sciences
Outcome results
None listed