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Clinical Trials in Turkey / NCT06862011
Active, not recruiting Not applicable

Evaluation of Sexual Health Counseling for Primiparous Pregnant Women Using PLISSIT Model and Motivational Interviewing

NCT06862011 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-03-15
Last updated
2025-04-25

Condition(s) studied

PregnancyPLISSIT ModelPrimiparity

Investigational drug(s) / intervention(s)

control group

control group: Only surveys will be filled out.

Study summary

This study is a simple randomized controlled intervention study to evaluate the effects of sexual counseling given to primiparous pregnant women using motivational interviewing on sexual self-efficacy, attitude towards sexuality and quality of sexual life.

HO: There is no difference between the mean Sexual Function Scale score in the last evaluation of pregnant women in the intervention and control groups.

H0a: There is no difference between the mean Sexual Self-Efficacy Scale score in the last evaluation of pregnant women in the intervention and control groups.

H0b: There is no difference between the mean Attitude Towards Sexuality During Pregnancy Scale score in the last evaluation of pregnant women in the intervention and control groups.

H0c: There is no difference between the mean Sexual Life Quality Scale score in the last evaluation of pregnant women in the intervention and control groups.

Eligibility

Sex
FEMALE
Min age
19 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Those over 19 years of age * Those in their first pregnancy * Those in their 8th-16th weeks of pregnancy * Those who are sexually active * Those who have a score of less than 26.55 on the Female Sexual Function Scale (FSFI) Exclusion Criteria: * Those who have given birth prematurely * Those who have developed a pregnancy complication that prevents coitus at any stage of the study (placenta previa, preterm premature rupture of membranes) * Those who do not comply with the study plan * Those who have received any sexual counseling * Those who have experienced a life crisis (death of partner, divorce, moving, etc.) * Those who want to withdraw from the study at any stage of the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Yıldırım Beyazıt University Ankara Turkey (Türkiye)

More Tokat Gaziosmanpasa University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06862011 on ClinicalTrials.gov ↗ ← All trials in Turkey