NCT07820306Not yet recruiting
Roy Adaptation Model-Based Prenatal Education in Hypertensive Pregnant Women
The Effect of Roy Adaptation Model-Based Prenatal Education on Perceived Stress and Quality of Life in Hypertensive Pregnant Women
Source: ClinicalTrials.gov · Last updated 23 Sept 2026
Brief summary (registry, in English)
This study aims to evaluate the effect of Roy Adaptation Model-based prenatal education on perceived stress and quality of life in pregnant women with hypertensive disorders of pregnancy. Pregnant women with hypertensive disorders who meet the eligibility criteria will be randomly assigned to either an intervention group or a control group. Participants in the intervention group will receive prenatal education based on the Roy Adaptation Model in two face-to-face sessions, one week apart. The control group will receive routine antenatal care. Blood pressure monitoring will be recommended for participants in both groups. Perceived stress and quality of life will be assessed before the education and after the intervention. The study will investigate whether Roy Adaptation Model-based prenatal education helps reduce perceived stress and improve quality of life among pregnant women with hypertensive disorders.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 54 (estimated)
- First submitted
- 10 Sept 2026
- Start date
- 16 Sept 2026
- Primary completion date
- 10 Jan 2027
- Lead sponsor
- Istanbul University - Cerrahpasa
- Diseases
- High blood pressure
- NCT number
- NCT07820306
What you commit to
- Study type: Interventional
- Planned participants: 54
- From 16 Sept 2026 to the primary completion date, 10 Jan 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Pregnant women with severe preeclampsia, eclampsia, HELLP syndrome, or a clinical condition requiring emergency obstetric intervention.
- Pregnant women with severe psychiatric, neurological, or cognitive impairment that may prevent participation in the education sessions or completion of the data collection instruments.
Other
- Pregnant women who are hospitalized or scheduled for hospitalization at the beginning of the study.
- Pregnant women diagnosed with fetal anomaly or intrauterine fetal death.
- Pregnant women who develop a serious obstetric or clinical complication during the study that may affect the primary outcomes of the study.
Who the study is looking for
- Pregnant women who apply to the antenatal outpatient clinic of the relevant hospital.
- Women diagnosed by a physician with a hypertensive disorder of pregnancy. Women who are between 20 and 32 weeks of gestation.
- Women aged 18 years or older.
- Primiparous or multiparous pregnant women.
- Women who can read and understand Turkish and communicate in Turkish.
- Women who are willing to participate in the study.
Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Prof.Dr.Cemil Taşcıoğlu Şehir Hastanesi Coordinator of this site? Confirm its status | Istanbul | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.