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Clinical Trials/NCT03741608
NCT03741608
Terminated
Not Applicable

A Mindfulness and Behavioral Intervention for Reducing Hypertension Among Women of Childbearing Age

University of Maryland, Baltimore4 sites in 1 country23 target enrollmentJanuary 22, 2019
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
University of Maryland, Baltimore
Enrollment
23
Locations
4
Primary Endpoint
Blood pressure reduction
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

This study will assess whether an intervention including mindfulness, dietary education, and smoking cessation can help African-American women of childbearing age (age 18-44) with hypertension or high blood pressure to lower their blood pressure. The investigators propose to screen women of childbearing age for hypertension, and to invite women to participate in an intervention to reduce their blood pressure. The investigators will track their perceived stress and their blood pressure levels over the next 6 months. Half of the women who participate will be given a blood pressure cuff and taught to measure their own blood pressure. More frequent tracking of blood pressure will be done in these women.

Detailed Description

Chronic and pregnancy-associated hypertension increase risk for poor birth outcomes, including higher rates of low birthweight and preterm birth. Mindfulness interventions, dietary education, and smoking cessation education have all been effectively employed to reduce hypertension, but have infrequently targeted women of childbearing age in community settings. This study will screen African-American women of childbearing age for hypertension, and invite women with hypertension to participate in a seven-session intervention to reduce blood pressure. The investigators will track their perceived stress and their blood pressure levels over the next 6 months. Half of the women who participate will be given a blood pressure cuff and taught to measure their own blood pressure. More frequent tracking of blood pressure will be done in these women.

Registry
clinicaltrials.gov
Start Date
January 22, 2019
End Date
April 1, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wendy Lane

Associate Professor

University of Maryland, Baltimore

Eligibility Criteria

Inclusion Criteria

  • Hypertension
  • Age 18-44
  • African-American

Exclusion Criteria

  • Age \<18 or \>44
  • Non-African American
  • Not female

Outcomes

Primary Outcomes

Blood pressure reduction

Time Frame: 6 months

decrease in systolic and diastolic blood pressure by 10 points each

Secondary Outcomes

  • Stress(6 months)

Study Sites (4)

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