Therapeutic Writing to Reduce Stress
- Conditions
- Pregnancy ComplicationsStress, PhysiologicalHigh Risk Pregnancy
- Registration Number
- NCT03904979
- Lead Sponsor
- University of North Carolina, Chapel Hill
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Suspended
- Sex
- Female
- Target Recruitment
- 15
Inclusion Criteria:<br><br> - Women will be prospectively recruited.<br><br> 1. Gestational age: All women presenting for prenatal care at 8.0 to 19.9 weeks'<br> gestation through the UNC-Hospitals High Risk obstetrics clinic will be<br> screened for high risk of an adverse pregnancy outcome (ex: preterm birth or<br> pre-eclampsia) through review of their medical record.<br><br> 2. Singleton viable intrauterine pregnancy, with dating confirmed by ultrasound or<br> plans for ultrasound to confirm dating prior to study enrollment<br><br> 3. No structural abnormalities or aneuploidy<br><br> 4. Ability to communicate in and provide consent in English<br><br> 5. Women with at least ONE of the following high risk criteria:<br><br> a. Short cervix by endovaginal ultrasound, measuring <25mm b. Prior spontaneous<br> preterm birth 16.0 - 33.9 weeks' gestation i. Documentation of the prior<br> spontaneous preterm birth in the patient's medical records is desirable but is<br> not required for eligibility.<br><br> ii. The previous preterm delivery cannot be an antepartum stillbirth but an<br> intrapartum stillbirth (due to extreme prematurity) is allowable.<br><br> c. Chronic hypertension on medications d. History of pre-eclampsia requiring<br> delivery <37 weeks' gestation, or history of severe pre-eclampsia delivering at<br> any gestational age<br><br> OR<br><br> 6. Women with at least TWO of the following moderate risk criteria:<br><br> 1. Prior preterm birth 34.0-36.9 weeks<br><br> 2. Chronic hypertension not requiring medications<br><br> 3. History of term pre-eclampsia<br><br> 4. Type II diabetes on insulin<br><br> 5. Obesity with a BMI >30<br><br> 6. Smoking during pregnancy<br><br> 7. Black race<br><br> 8. Maternal age <18 years old or >40 years old<br><br> 9. Nulliparous<br><br> 10. Uninsured, or medicaid insurance<br><br> 7. Women who meet at least one major or 2 minor inclusion criteria along with the<br> other criteria above will then be screened for high levels of acute and chronic<br> stress and trauma using the Perceived Stress questionnaire to determine final<br> eligibility for the study<br><br>Exclusion Criteria:<br><br> 1. Persistent Illicit drug or alcohol abuse during current pregnancy >12 weeks. Use of<br> tobacco and/or marijuana is not an exclusion. Methadone or suboxone use in an<br> approved treatment program is not an exclusion.<br><br> 2. Prior preterm birth or preeclampsia was in a pregnancy complicated by fetal<br> aneuploidy or major congenital fetal anomalies in the absence of another pregnancy<br> meeting above inclusion criteria<br><br> 3. Major congenital anomaly such as major structural deficit of the heart, lungs, or<br> brain or aneuploidy<br><br> 1. Mild renal abnormalities, clubfoot, isolated cleft lip/palate, etc. in the<br> fetus are not a reason for exclusion<br><br> 2. For a detailed list of major anomalies, see Table 3 - Major Fetal Anomalies /<br> Congenital Malformations, below. Two or more minor anomalies observed together<br> (see Table 2 - Minor Fetal Anomalies / Congenital Malformations) count as a<br> major anomaly<br><br> 3. Isolated 'soft markers' for aneuploidy (such as choroid plexus cysts, echogenic<br> bowel, etc.) are not a reason for exclusion<br><br> 4. If aneuploidy screening is performed, any aneuploidy screen positive test with<br> a risk for aneuploidy greater than 1 in 25 without negative confirmatory<br> definitive aneuploidy testing is reason for exclusion<br><br> 4. Spanish speaking women<br><br> 5. Women participating in other intervention-based studies
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percent Participation in Writing Activity;Statistically significant improvement (reduction) in the Perceived Stress Scale Score;Proportion of women with adverse perinatal outcomes;Change in pro-inflammatory biomarkers in maternal blood by randomization group;Change in pro-inflammatory biomarkers in maternal blood by outcome;Change in stress-related gene expression in maternal blood by randomization group;Change in stress-related gene expression in maternal blood by outcome
- Secondary Outcome Measures
Name Time Method Utilization of professional psychiatric care;Stress related pathways gene expression - placental tissue - by randomization group;Stress related pathways gene expression - placental tissue - by diagnosis of adverse perinatal outcome;Rate of preterm birth less than 37 weeks' gestation by randomization group;Rate of diagnosis of intrauterine growth restriction, using sex-specific curves, by randomization group;Rate of diagnosis of preeclampsia by randomization group;Rate of diagnosis of placental abruption by randomization group