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The effect of sexual counseling on sexual function in pregnant women

The effect of virtual based cognitive-behavioral sexual counseling on sexual function, satisfaction and intimacy in pregnant women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20161230031662N10
Enrollment
80
Registered
2021-06-21
Start date
2021-05-20
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

Pregnancy. Counseling related to sexual attitude

Interventions

Intervention 1: Intervention group: Eight weekly 90-minute group sex counseling sessions with virtual content based on cognitive behavioral therapy. First, a group will be formed in one of the messagi

Sponsors

Vice chancellor for research Alborz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Sexual function score less than 28 First pregnancy Single pregnancy Wanted pregnancy Gestational age 16 to 24 weeks Low risk pregnancy Having access to a phone with Android operating system Internet literacy Age 18 to 35 years No grief in the three months before the study Living with a spouse

Exclusion criteria

Exclusion criteria: High risk pregnancies such as placenta previa, threatened miscarriage, gestational hypertension, gestational diabetes and high risk screening Smoking and drinking alcohol Use of drugs and drugs that affect sexual response Sexual dysfunction in the spouse Severe mental illness Attend similar treatment sessions for the past six months

Design outcomes

Primary

MeasureTime frame
Sexual function score in Rosen's female sexual performance questionnaire. Timepoint: In two turns, before the study begins and four weeks after the end of intervention. Method of measurement: Rosen women's sexual function questionnaire.

Secondary

MeasureTime frame
Sexual satisfaction score in the Larson questionnaire. Timepoint: At the beginning of the study and four weeks the end of the study. Method of measurement: Larson sexual satisfaction questionnaire.;Sexual intimacy score in the in the Botlani questionnaire. Timepoint: At the beginning of the study and four weeks after the end of the study. Method of measurement: Botlani sexual intimacy questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactManizheh Fathalian

Karaj University of Medical Sciences

mahtab.fathi358@gmail.com+98 26 3419 7685

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 14, 2026