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The effectiveness of structured education on sexual function of pregnant women

The Effect of Structural Education on the Sexual Function of Pregnant Women Referred to Health Centers in Baharestan

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140907019077N14
Enrollment
80
Registered
2018-03-19
Start date
2017-10-23
Completion date
Unknown
Last updated
2018-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Female sexual function during pregnancy. Unspecified sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: Intervention group: First, the sexual performance questionnaire is completed by the mothers and their sexual function is measured. Then, participants participate in educational session

Sponsors

Vice Chancellor for research of Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Pass at least 4 weeks after giving birth to the mother Maximum gestational age 34 weeks

Exclusion criteria

Exclusion criteria: There is a history of preterm labor There is a history of cervical failure The presence of Placenta Previa

Design outcomes

Primary

MeasureTime frame
Sexual function. Timepoint: Before and two weeks after intervention. Method of measurement: Female sexual function index questionnaire.

Secondary

MeasureTime frame
Desire. Timepoint: Before and two weeks after intervention. Method of measurement: Female sexual function index questionnaire.;Arousal. Timepoint: Before and two weeks after intervention. Method of measurement: Female sexual function index questionnaire.;Lubrication. Timepoint: Before and two weeks after intervention. Method of measurement: Female sexual function index questionnaire.;Orgasm. Timepoint: Before and two weeks after intervention. Method of measurement: Female sexual function index questionnaire.;Satisfaction. Timepoint: Before and two weeks after intervention. Method of measurement: Female sexual function index questionnaire.;Pain. Timepoint: Before and two weeks after intervention. Method of measurement: Female sexual function index questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnaz esmaili

Qazvin University Of Medical Sciences

mhs_1924@yahoo.com+98 21 5633 2239

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 1, 2026