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Improving Patient Understanding of Macrosomia

Improving Patient Understanding of Macrosomia: a Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06281301
Enrollment
222
Registered
2024-02-28
Start date
2024-01-30
Completion date
2024-07-06
Last updated
2024-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Macrosomia, Fetal

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.

Interventions

Participants will have 15 minutes to review the single sided card and then the survey will be administered. Participants will then be surveyed again within 1-2 weeks after initial completion to assess how well information was retained.

OTHERno additional information

Survey will be administered without reviewing the single sided card

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* singleton pregnancy * greater than or equal to 36 weeks gestation.

Exclusion criteria

* unable to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026