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Daily Meditation Program in Women Admitted to the Antepartum Unit

NCT03737279 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2020-06-16

No results posted yet for this study

Summary

The purpose of this study is to assess whether a daily mindful meditation program for women admitted to the antepartum floor will decrease maternal state anxiety compared to routine care.

Conditions

  • Pregnancy, High Risk
  • Pregnancy Related

Interventions

BEHAVIORAL

Meditation

Routine care + twice daily meditation per schedule, to start on the day of randomization

BEHAVIORAL

Routine Care

Routine care including ACOG educational pamphlets: * Day 1: "Nutrition in Pregnancy" * Day 2: "Heart Health for Women" * Day 3: "Exercise after Pregnancy"

Sponsors & Collaborators

  • The University of Texas Health Science Center, Houston

    lead OTHER

Principal Investigators

  • Morgen S Doty, DO · The University of Texas Health Science Center, Houston

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-03-04
Primary Completion
2020-04-01
Completion
2020-04-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03737279 on ClinicalTrials.gov