- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01119183
Improving Patient Understanding of Preeclampsia
June 9, 2022 updated by: Northwestern University
Participants counseled with the preeclampsia educational tool will have a better understanding of preeclampsia than those not counseled using the tool.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60611
- Northwestern University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: 2
|
The ACOG pamphlet on preeclampsia will be offered to this group
|
|
Experimental: 3
|
The newly created preeclampsia educational tool will be offered to this group
|
|
No Intervention: 1
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improved understanding of preeclampsia
Time Frame: one week
|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2010
Primary Completion (Actual)
July 1, 2010
Study Completion (Actual)
July 1, 2010
Study Registration Dates
First Submitted
April 23, 2010
First Submitted That Met QC Criteria
May 5, 2010
First Posted (Estimate)
May 7, 2010
Study Record Updates
Last Update Posted (Actual)
June 13, 2022
Last Update Submitted That Met QC Criteria
June 9, 2022
Last Verified
June 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STU00006039
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Preeclampsia
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-
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University Medical Centre LjubljanaCompletedPreeclampsia Postpartum | Preeclampsia SevereSlovenia
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Anna Stanhewicz, PhDActive, not recruiting
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Cedars-Sinai Medical CenterThermoFisher Scientific Brahms Biomarkers FranceCompletedGestational Hypertension | Preeclampsia Severe | Preeclampsia and Eclampsia | Chronic Hypertension in Obstetric Context | Superimposed Pre-Eclampsia | Preeclampsia MildUnited States
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Clinical Trials on ACOG education pamphlet on preeclampsia
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Hamad Medical CorporationNot yet recruiting
-
Université de SherbrookeUniversity of OttawaCompleted
-
Rush University Medical CenterCompleted
-
Tel-Aviv Sourasky Medical CenterUnknown
-
Columbia UniversityNational Institute of Neurological Disorders and Stroke (NINDS)Completed
-
University of MiamiUniversity of Miami CTSICompleted
-
University of WindsorCanadian Institutes of Health Research (CIHR)Completed
-
Medstar Health Research InstituteCompletedHypertension in Pregnancy | Postpartum PreeclampsiaUnited States
-
Istanbul University - Cerrahpasa (IUC)RecruitingPreeclampsia | Healthy Lifestyle | Pregnancy; Renal DiseaseTurkey
-
The Hong Kong Polytechnic UniversityCompleted