App-based remote blood pressure monitoring for Hypertension

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Women & Infants Hospital of Rhode Island, Providence, RIHypertension+2 MoreApp-based remote blood pressure monitoring - Behavioral
Eligibility
18 - 55
Female
What conditions do you have?
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Study Summary

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.

Eligible Conditions
  • Pregnancy-Induced Hypertension
  • Prophylaxis of Preeclampsia
  • Pregnancy-Induced Hypertension (PIH)

Treatment Effectiveness

Effectiveness Progress

1 of 3

Study Objectives

1 Primary · 5 Secondary · Reporting Duration: 3-10 days postpartum

3-10 days postpartum
Blood pressure ascertainment
Day 40
Agency for Healthcare Research and Quality Consumer Assessment of Healthcare Providers and Systems survey (AHRQ CAHPS)
Decisional Regret Scale
Week 6
Adherence to evidence-based practice
Postpartum severe maternal morbidity composite
Day 30
Hypertensive disease

Trial Safety

Safety Progress

1 of 3

Trial Design

2 Treatment Groups

Text-message based remote blood pressure monitoring
1 of 2
App-based remote blood pressure monitoring
1 of 2

Active Control

Experimental Treatment

120 Total Participants · 2 Treatment Groups

Primary Treatment: App-based remote blood pressure monitoring · No Placebo Group · N/A

App-based remote blood pressure monitoring
Behavioral
Experimental Group · 1 Intervention: App-based remote blood pressure monitoring · Intervention Types: Behavioral
Text-message based remote blood pressure monitoring
Behavioral
ActiveComparator Group · 1 Intervention: text-message based remote blood pressure monitoring · Intervention Types: Behavioral

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: 3-10 days postpartum

Who is running the clinical trial?

Women and Infants Hospital of Rhode IslandLead Sponsor
100 Previous Clinical Trials
36,634 Total Patients Enrolled
Adam Lewkowitz, MD, MPHSPrincipal InvestigatorWomen and Infants Hospital of Rhode Island

Eligibility Criteria

Age 18 - 55 · Female Participants · 5 Total Inclusion Criteria

Mark “Yes” if the following statements are true for you:
You must have a smartphone to measure your blood pressure remotely.

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

Unverified Answer

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

Unverified Answer

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

Unverified Answer

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

Unverified Answer
Please Note: These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.