sexual dysfunction.
Conditions
Interventions
Intervention 1: Intervention group1: Group members will be instructed to walk 30 to 60 minutes three times a week and submit to the relevant checklist. Intervention 2: Intervention group 2: People wil
Sponsors
Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: lactating women without unknown psychiatric problems or systemic illness which have an effect on sexual function; Stressful events have not occurred to them in the last 6 months; Married and live with a permanent partner; use a safe contraceptive method, during lactation (40 days to 6 months postpartum); have exclusive breastfeeding; total score = 28 from the Rosen Sexual function Questionnaire; have ability to contract pelvic floor muscles and Singleton delivery.
Exclusion criteria
Exclusion criteria: Drug dependence , Marital discord, Unwillingness to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Score of sexual function in Rosen Female Sexual Function Index. Timepoint: Before intervention and 3 months after intervention. Method of measurement: Completion of Rosen Women's Sexual Function Index. | — |
Secondary
| Measure | Time frame |
|---|---|
| ????. Timepoint: ????. Method of measurement: ????. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSousan Heydarpour
Kermanshah University of Medical Sciences
Outcome results
None listed