Sexual dysfunction in women newly delivered. Unspecified sexual dysfunction, not caused by organic disorder or disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Having at least a literacy guide according to the person herself Score less than 28 from the Female Sexual Function Index questionnaire (FSFI ) Single lactating women Being between 3 and 6 months after childbirth Having a call number to follow up Husband's monogamous
Exclusion criteria
Exclusion criteria: Exposure to a stressful event or any complication of pregnancy during pregnancy and postpartum (for example: death of a family members) according to the person herself Having a history of depression pre-pregnancy, during pregnancy and postpartum according to the person herself Having a history of chronic physical and mental illness such as cardiovascular disease, diabetes, severe depression and high blood pressure that consumes the drug according to the person herself Use of any effective medicines on person's sexual response, (antihypertensive drugs, thiazide diuretics, antidepressants, antihistamines, Barbiturates, narcotics, diazepins, amphetamines and cocaine) according to the person herself Child with known anomalies or preterm (less than 37 weeks) Marriage separation (emotional divorce or full divorce) The death of the baby after delivery for any cause Addiction to a person or his wife according to the person herself The history of sexual dysfunction before pregnancy in couples (including disorders of sexual desire or orgasm in women, early and late ejaculation, erectile dysfunction and male orgasm) according to the person herself
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual function score. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Female Sexual Function Index questionnaire.;Marital satisfaction score. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Enrich Marital Satisfaction questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of sexual life score. Timepoint: Before the intervention, 4 and 8 weeks after the intervention. Method of measurement: Female sexual quality of life questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University of Medical Sciences