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To Determine the Effect of Education of Sexual Health Promotion Package in Woman During Pregnancy

The Study of Effect of Education of Sexual Health Promotion Package on Sexual Health Dimensions of Pregnant Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190427043398N1
Enrollment
225
Registered
2019-06-02
Start date
2018-09-01
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Sexual Health. Sex counseling, unspecified

Interventions

Intervention 1: First Intervention group: Face-to-Face training is provided to pregnant women in three sessions -90 minute- during pregnancy (first session in the first trimester, second session in th
through lecture, Question and Answer training provided by the researcher. The Sexual Health Package was designed based on the clinical guidelines of NICE. According to this pattern, the package was de

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: gestational age less than 14 weeks; women’s age between 15- 45 years; Having informed consent to participate in the study; Lack of history of medical diseases; lack of consumption of the medication that affect sexual function; lack of drug addiction; lack of high risk pregnancy criteria; lack of experience of an acute stress during recent years such as child’s death, acute illness, etc.

Exclusion criteria

Exclusion criteria: Unwillingness of pregnant women to participate in the study

Design outcomes

Primary

MeasureTime frame
Sexual Response in pregnancy. Timepoint: Before intervention; At the beginning of each subsequent intervention; Four weeks after the last intervention. Method of measurement: Pregnancy Sexual Response Inventory (PSRI).;Sexual function. Timepoint: Before intervention; At the beginning of each subsequent intervention; Four weeks after the last intervention. Method of measurement: Female Sexual Function Index (FSFI).;Sexual Quality of life. Timepoint: Before intervention; At the beginning of each subsequent intervention; Four weeks after the last intervention. Method of measurement: Sexual Quality of life Questionnaire.;Sexual Violence. Timepoint: Before intervention; At the beginning of each subsequent intervention; Four weeks after the last intervention. Method of measurement: Sexual Violence Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShiva Alizadeh

Shahid Beheshti University of Medical Sciences

shiva.alizadeh@sbmu.ac.ir+98 21 8820 2512

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 23, 2026