MedPath

Improving Patient Understanding of Macrosomia

Not Applicable
Completed
Conditions
Macrosomia, Fetal
Registration Number
NCT06281301
Lead Sponsor
The University of Texas Health Science Center, Houston
Brief Summary

The purpose of this study is to evaluate the effectiveness of a graphic based education tool on patient knowledge of macrosomia through the use of a survey and to evaluate knowledge at 1-2 weeks after initial review of the education tool.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
222
Inclusion Criteria
  • singleton pregnancy
  • greater than or equal to 36 weeks gestation.
Exclusion Criteria
  • unable to provide informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Number of participants that showed Macrosomia knowledge as assessed by the score on a surveyimmediately after intervention (about 5 minutes after intervention)

This survey has 17 questions and will be scored from 1-17 higher number indicating better outcome

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

The University of Texas Health Science Center at Houston

🇺🇸

Houston, Texas, United States

The University of Texas Health Science Center at Houston
🇺🇸Houston, Texas, United States

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