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NCT01119183 Clinical Trial

Improving Patient Understanding of Preeclampsia

Preeclampsia Clinical Trial

Official title:
Improving Patient Understanding of Preeclampsia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01119183
Other study ID # STU00006039
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 2010
Est. completion date July 2010

Study information
Verified date June 2022
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Participants counseled with the preeclampsia educational tool will have a better understanding of preeclampsia than those not counseled using the tool.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date July 2010
Est. primary completion date July 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - 12-40 weeks pregnant - No significant hearing or vision impairment - English speaking Exclusion Criteria: - Active diagnosis of preeclampsia - Significant hearing or vision impairment - Non-English speaking

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• ACOG education pamphlet on preeclampsia
The ACOG pamphlet on preeclampsia will be offered to this group
• Preeclampsia education tool
The newly created preeclampsia educational tool will be offered to this group

Locations
Country Name City State
United States Northwestern University Chicago Illinois

Sponsors (1)
Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Improved understanding of preeclampsia Understanding of preeclampsia will be assessed through a questionnaire that asks a series of closed ended questions about preeclampsia as well as a single open ended question. This questionnaire has been used in a prior study and has proven to be a useful assessment of patient knowledge. one week
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