This trial showed that a program using text messages, Bluetooth-enabled cuff & AI can provide tailored hypertension support & reduce cost for postpartum blood pressure checks.
- Pregnancy-Induced Hypertension
- Prophylaxis of Preeclampsia
- Pregnancy-Induced Hypertension (PIH)
1 Primary · 5 Secondary · Reporting Duration: 3-10 days postpartum
2 Treatment Groups
Text-message based remote blood pressure monitoring
1 of 2
App-based remote blood pressure monitoring
1 of 2
120 Total Participants · 2 Treatment Groups
Primary Treatment: App-based remote blood pressure monitoring · No Placebo Group · N/A
Who is running the clinical trial?
Age 18 - 55 · Female Participants · 5 Total Inclusion CriteriaMark “Yes” if the following statements are true for you:
Frequently Asked Questions
Does this research accept participants 45 years of age or above?
"This trial seeks participants between 18 and 55 years of age. Alternatively, there are 69 trials for minors and 713 specifically targeting seniors." - Anonymous Online Contributor
Are there any eligibility requirements for participation in this research?
"This medical trial is recruiting 120 individuals with pre-eclampsia aged between 18 and 55. English or Spanish language proficiency, a history of gestational hypertension, preeclampsia or chronic hypertension, smartphone ownership for remote blood pressure monitoring, and postpartum care at a Women & Infants Hospital (WIH)-affiliated clinic are some of the criteria necessary to be eligible for this study." - Anonymous Online Contributor
Are there openings for participants in this investigation?
"Data on clinicaltrials.gov reveals that this investigation is actively recruiting patients; it was first published the 7th of November 2022 and updated later on the 15th of same month." - Anonymous Online Contributor
How many participants are being incorporated into this experiment?
"Affirmative. Data on clinicaltrials.gov states that this study is actively searching for candidates and has been since it was initially posted on November 7th 2022. The trial needs 120 participants from a single site, with the information most recently updated on November 15th of the same year." - Anonymous Online Contributor