Actively Recruiting
Sexual Health Education During Pregnancy
Led by Ordu University · Updated on 2026-04-08
70
Participants Needed
1
Research Sites
37 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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).
CONDITIONS
Official Title
Sexual Health Education During Pregnancy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Volunteers willing to participate in the research
- Primary school graduate
- Pregnant between 16 and 20 weeks of gestation
- Having a single pregnancy
- Able to understand and speak Turkish
- Living with spouse for the past four weeks
- No threat of abortion or premature birth
You will not qualify if you...
- Diagnosed with a chronic illness
- Having diagnosed physical or mental health issues
- Diagnosed with a psychological disorder
- Having a high-risk pregnancy
- Having an IVF pregnancy
- Having low pregnancy threat
- Diagnosed with any sexually transmitted disease in self or partner
- Using medications that may negatively affect sexual function, including antipsychotics, antihypertensives, phenobarbital, and opioids
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Ordu University
Altinordu, Ordu, Turkey (Türkiye), 52200
Actively Recruiting
Research Team
G
Gizem YILDIZ, MSc
CONTACT
G
Gizem YILDIZ, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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