Sexual function and satisfaction problems in pregnant women. Encounter for supervision of normal pregnancy
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Singleton pregnancy without serious medical complications Gestational age between 12 and 24 weeks at enrollment. Access to the internet and a smart device to participate in online sessions Willingness and ability to attend all intervention sessions. Absence of severe or persistent psychiatric disorders. Provision of written informed consent.
Exclusion criteria
Exclusion criteria: Occurrence of any serious pregnancy complications during the study. Withdrawal from the study. Absence from more than one intervention session.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual function of pregnant women will be measured using the total score of the Female Sexual Function Index (FSFI). Timepoint: Baseline: one day before the intervention Post-intervention: immediately after completion of the intervention Follow-up: two months after the intervention. Method of measurement: The FSFI questionnaire will be completed online, and the total sexual function score will be calculated. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sexual satisfaction of pregnant women will be measured using the Larson Sexual Satisfaction Questionnaire. Timepoint: Baseline: one day before the intervention Post-intervention: immediately after completion of the intervention Follow-up: two months after the intervention. Method of measurement: The Larson Sexual Satisfaction Questionnaire will be completed online. | — |
Countries
Iran (Islamic Republic of)
Contacts
Torbate-Heidaria University of Medical Sciences