- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00182325
Effects of a Personalized Web-based Antenatal Care Planner
Women's Web Access to Their Own Antenatal Health Record and Personalized Health Information: Effect on Pregnancy Health Outcomes and Patient Satisfaction
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Many women are turning to the Internet to meet their health information needs, but the large amount of information available, as well as the unknown reliability and applicability of information can be overwhelming. Studies in specific patient populations have determined that patients given access to personalized, on-line medical information are more satisfied with their care than patients provided generalized information. None of these studies have looked at whether this type of patient education would be helpful for pregnant women. This study is being done to determine whether pregnant women who have access to their own health records and personalized health information over the Internet are more satisfied with their prenatal care, and if they are more compliant with health visits and tests, compared to pregnant women who receive only generic pregnancy information on the Internet and from pamphlets
Women are being randomly assigned to receive secure access to pregnancy health information links chosen by the centre's physicians, or to receive these links with access to their online personal health that includes the antenatal record and a section of their care planner, from the centre's electronic medical record
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ontario
-
Hamilton, Ontario, Canada, L8N 3Z5
- McMaster University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- less than 28 weeks pregnant access to Internet
Exclusion Criteria:
- cannot speak/read English and no translator
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: personalized web prenatal information
Personalized health information for pregnancy through personal health record
|
|
|
Active Comparator: general web prenatal information
General pregnancy health related websites
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Uptake of Service
Time Frame: 11 months
|
Number of log-ins
|
11 months
|
|
Easy to Log on
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Information Easy to Understand
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Learned Something New
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Easy to Find Information
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Stay Healthy
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Learn About Risks
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Understand Tests
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Make Decisions
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
|
Helped me Remember Appointments
Time Frame: 11 months
|
Women were asked to rate their agreement with statements about the website from strongly agree (1) to strongly disagree (5) on a five-point scale.
Results presented here are mean responses to questionnaire about the pregnancy website in the two randomized groups.
|
11 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Heather Waters, MD, McMaster University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- RDF-160
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