Evaluation of blood pressure measurement software that is integrated with a digital pregnancy record and decision-support system to improve high blood pressure detection and pregnancy outcomes in Indonesia
Not Applicable
Completed
- Conditions
- Hypertensive disorders in pregnancyCirculatory System
- Registration Number
- ISRCTN58479805
- Lead Sponsor
- SUMMIT Institute for Development
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 5660
Inclusion Criteria
Health workers and trained laypersons:
1. Age 18-55 years
2. Health workers or trained laypersons in the catchment area who provide antenatal care services
3. Informed consent
Pregnant women:
1. Pregnant women of any gestational age
2. Informed consent
Exclusion Criteria
Health workers and trained laypersons:
1. Health workers or trained laypersons who cannot operate Android-based applications
Pregnant women:
1. Does not meet the inclusion criteria
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The rate of ‘correct’ action measured using WHO’s guidance on appropriate management of elevated blood pressure in pregnancy as the comparison at the end of data collection period (6 months)
- Secondary Outcome Measures
Name Time Method 1. The proportion of ANC contacts in which BP is captured consistently, measured by dividing all ANC visits with overall enrollment over 6 months of data collection<br>2. The proportion of pregnant women detected by OptiBP receiving counseling, measured by dividing counseling attendance with all pathological cases that require counseling over 6 months of data collection<br>3. The proportion of pregnant women receiving referrals (treatment and/or proteinuria lab test), measured by dividing numbers of referrals with all pathological cases that require referral over 6 months of data collection