Skip to content

Investigating the effect of educational intervention on the sexual performance of women living in the marginal areas of eastern Iran

The effect of educational intervention on the sexual performance of marginalized women in eastern Iran

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20231121060133N1
Enrollment
76
Registered
2023-12-01
Start date
2024-06-04
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Educational needs on sexual dysfunction. Sexual dysfunction not due to a substance or known physiological condition

Interventions

Intervention 1: Intervention group: Sex education programs in this study were implemented in Three 120-minute sessions with an interval of one week. And it was presented in the form of lectures, quest

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: 1-Women aged 15-49 2- Married and currently living with his wife 3- He should not have acute communication problems with his wife 4- Not during pregnancy and breastfeeding 5- Be a resident of marginal areas 6- Not suffering from a known physical or mental illness 7- Not suffering from severe depression (score less than 29 in the Beck BID-II questionnaire) 8- Having sexual activity in the past month 9-Sexual function disorder in the person (female sexual function score of 26 or less (FSFI). 10-According to the woman's statement, her husband does not have any sexual dysfunction. 11- It is possible to reach the person within the next 4 months 12- He has not participated in any written training course related to marital problems

Exclusion criteria

Exclusion criteria: 1- The individual's unwillingness to continue attending the study 2- Occurrence of pregnancy during the study period 3- Occurrence of severe family disputes with spouse during the study period 4- The occurrence of unfortunate and stressful events during the study period (such as death of parents, death of children, etc.)

Design outcomes

Primary

MeasureTime frame
Changes in sexual performance scores between the two groups. Timepoint: 12 weeks after the last intervention session. Method of measurement: FSFI questionnaire.

Secondary

MeasureTime frame
The quality of a woman's sexual life. Timepoint: 12 weeks after the end of the intervention. Method of measurement: Questionnaire of Sexual Quality of Life–Female.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Ebrahimi

Tehran University of Medical Sciences

Ebrahimi-308@yahoo.com+98 21 6692 7171

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026