MedPath

Therapeutic Writing to Reduce Stress

Not Applicable
Suspended
Conditions
Pregnancy Complications
Stress, Physiological
High 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

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

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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
NameTimeMethod
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
© Copyright 2025. All Rights Reserved by MedPath