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Effect of counseling on sexual function of pregnant women

Effect of PLISSIT-based Counseling on Sexual Function of Pregnant Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015100324325N1
Enrollment
86
Registered
2016-01-22
Start date
2015-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

sexual function. Unspecified sexual dysfunction, not caused by organic disorder or diseas

Interventions

Intervention 1: control group, at first The FSFI questionnaire was completed by patients and measured level of sexual function in people. In this group the subjects not given counseling and special tr
control group, at first The FSFI questionnaire was completed by patients and measured level of sexual function in people. In this group the subjects not given counseling and special training and just
intervention group, at first the FSFI questionnaire in order to assess the sexual function completed with intervention group. Then participate in counseling sessions. For individual counseling are usi

Sponsors

Vice Chancellor for research Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: consent to participate in the study; gestational age between 8-10 weeks; First pregnancy and living in the city of Razan. Exclusion criteria: any problem during study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

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

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Kaboudi

Kermanshah University of Medical Sciences, School of Nursing and Midwifery

fkaboudi@kums.ac.ir+98 83 3827 9394

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026