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N/A N=193 Randomized Other

Effects of a Personalized Web-based Antenatal Care Planner

Pregnancy

Enrolled (actual)
193
Serious AEs
0.0%
Results posted
Jun 2019
Primary outcome: Primary: Uptake of Service — 10.4; 1.8 Log-ins — p=<0.0001

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
personalized web prenatal information (Behavioral); general web prenatal information (Behavioral)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
Hamilton Health Sciences Corporation
Primary completion
Aug 2006

Outcome Measures

OutcomeResultp-value
PRIMARY
Uptake of Service
10.4; 1.8 <0.0001 sig
PRIMARY
Easy to Log on
1.4; 1.5 0.84
PRIMARY
Information Easy to Understand
1.4; 1.5 0.68
PRIMARY
Learned Something New
1.8; 1.9 0.67
PRIMARY
Easy to Find Information
1.9; 1.8 0.57
PRIMARY
Helped me Stay Healthy
1.8; 1.6 0.17
PRIMARY
Helped me Learn About Risks
1.9; 1.8 0.46
PRIMARY
Helped me Understand Tests
1.7; 1.6 0.57
PRIMARY
Helped me Make Decisions
2.1; 2.4 0.26
PRIMARY
Helped me Remember Appointments
2.9; 3.5 0.12

Summary

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

Eligibility Criteria

Inclusion Criteria

  • less than 28 weeks pregnant access to Internet

Exclusion Criteria

  • cannot speak/read English and no translator
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00182325). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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