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Sexuality education in Postpartum

Not Applicable
Conditions
Sexual self efficacy.
Other sex counseling
Registration Number
IRCT201107086976N1
Lead Sponsor
Tehran University of Medical Sciences, School of Nursing Midwifery
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
200
Inclusion Criteria

Nulliparous women with permanent or temporary marriage; having a healthy pregnancy and uncomplicated vaginal delivery, after 6 hours of their birth; lack of physical and mental well-known disease; formally signing consent form for study participation and being literate.
Exclusion criteria: No consent or withdrew from the study at any time; any complications such as bleeding after childbirth, early or late; any condition that interferes with the participation of mothers in the intervention, such as jaundice, neonatal hospitalization for any reason; breastfeeding problems: breast lesions, mastitis; couples with temporary separation, marital discord or separation and sever chronic or acute illnesses.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual self efficacy. Timepoint: Eight weeks after intervention. Method of measurement: Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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