Status:
NOT_YET_RECRUITING
Home Assessment of Blood Pressure in PregnancY
Lead Sponsor:
University of British Columbia
Collaborating Sponsors:
Women's Health Research Institute of British Columbia
Providence Healthcare
Conditions:
Hypertensive Disorder of Pregnancy
Eligibility:
FEMALE
19+ years
Brief Summary
The goal of this observational study is to evaluate the feasibility and safety of a comprehensive home blood pressure telemonitoring (HBPT) program for pregnant people with hypertensive disorders of p...
Eligibility Criteria
Inclusion
- Adult patients aged ≥ 19 years
- Pregnancy
- Gestational age 20+0 to 36+0 weeks gestational age
- Diagnosed with gestational hypertension (defined as SBP ≥140 mm Hg and/or DBP ≥ 90 mm Hg) after 20 weeks gestation OR Chronic hypertension (defined as SBP ≥140 mm Hg and/or DBP ≥ 90 mm Hg), present at booking or before 20 weeks gestation, or receiving treatment (including lifestyle measures) prior to pregnancy and/or at time of referral OR Transient elevated office BP reading (defined as one time reading of SBP ≥140 mm Hg and/or DBP ≥ 90 mm Hg with risk factors for HDP as per Canadian guidelines).
- Participant is willing and able to give informed consent for participation in the study
- Able and willing to comply with study requirements
- Has smart phone
Exclusion
- Anticipated inpatient admission
- Remaining pregnancy less than 2 weeks duration
- Imminent delivery (within the next 48 hours)
- Non-English speaking or no family members who can help translate
Key Trial Info
Start Date :
July 1 2024
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 1 2026
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT06491199
Start Date
July 1 2024
End Date
January 1 2026
Last Update
July 9 2024
Active Locations (1)
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1
University of British Columbia
Vancouver, British Columbia, Canada, V5Z1M9