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Clinical Trials in Turkey / NCT07517549
Recruiting Not applicable

Sexual Health Education During Pregnancy

NCT07517549 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-15
Last updated
2026-04-08

Condition(s) studied

SexualityDepressionPregnancy Related

Investigational drug(s) / intervention(s)

sexuality health education group

sexuality health education group: This study will provide sexual counseling to pregnant women. Results will be collected both before delivery and at 3 months postpartum. The difference is that it covers both the pregnancy and postpartum periods.

Study summary

This experimental, randomized controlled, single-blind study includes intervention and control groups. Pregnant women between 16 and 20 weeks of gestation who meet the inclusion criteria and agree to participate will be included in the study. Pregnant women will be randomly assigned to groups. Pre-test data will be collected from both groups. The intervention group will receive sexual counseling training in two sessions, face-to-face and in groups, until week 22. Second test data will be collected after week 37 (before delivery), and final test data will be collected three months after delivery. This study is expected to have a significant impact on women's lives, as this topic is considered taboo in our country, leading to a lack of open discussion and the prevalence of misconceptions and false beliefs (sexual myths).

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Eligibility criteria; * Volunteers to participate in the research, * primary school graduate, * Pregnant between 16-20 weeks * Having a single pregnancy, * Able to understand and speak Turkish, * Living with his wife for the past four weeks, * No threat of abortion or premature birth, Exclusion Criteria: * Someone who has been diagnosed with a chronic illness, * People with diagnosed physical and mental health issues, * Someone who has been diagnosed with a psychological disorder, * Having a high-risk pregnancy, * Having an IVF pregnancy, * Low threat, * Anyone who has been diagnosed with any sexually transmitted disease, either themselves or in their partner, * Those using medications that may negatively affect sexual function, * including antipsychotics, antihypertensives, phenobarbital, and opioids.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ordu University Altinordu Ordu Recruiting

More Ordu 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 NCT07517549 on ClinicalTrials.gov ↗ ← All trials in Turkey