COMPLETED

Social Risks-Focused Lifestyle Intervention to Reduce Preeclampsia (SAIL)

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Preeclampsia is a disease of pregnancy and first few weeks after birth. It is diagnosed as new onset of high blood pressure and injury to organs such as kidneys, liver, and brain. Preeclampsia is growing at a rapid rate - rate that exceeds diabetes and heart disease. Over half a million lives lost each year to preeclampsia. Women with a history of preeclampsia have 3-4 times the risk of high blood pressure. They also have double the risk for heart disease and stroke. Racial and ethnic disparities are present in preeclampsia. Black women are at higher risk of developing preeclampsia. They are also at much higher risk of dying from preeclampsia than other women. The reasons behind such disparities are unclear. What may explain these differences are social determinants of health. The contribution of social determinants to differences in preeclampsia is well recognized. However, a major gap in research remains strategies that address these factors. Our study will test a lifestyle intervention incorporating social risk factors to reduce the risk of preeclampsia.

Official Title

Social Risks-Focused Lifestyle Intervention to Reduce Preeclampsia in AA Women

Quick Facts

Study Start:2022-03-28
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT04958057

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 45 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * self-report as African-American/Non-Hispanic black
  2. * residence in inner-city Milwaukee
  3. * nulliparity
  4. * gestational age at enrollment \<=16 weeks
  5. * able and willing to give informed consent
  1. * not able to communicate in English
  2. * major fetal anomaly
  3. * psychiatric illness that precludes group participation

Contacts and Locations

Study Locations (Sites)

Medical College of Wisconsin
Wauwatosa, Wisconsin, 53226
United States

Collaborators and Investigators

Sponsor: Medical College of Wisconsin

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-03-28
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2022-03-28
Study Completion Date2024-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Preeclampsia