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NCT05236725 · ClinicalTrials.gov registry record · NA
Monitoring and Testing of Blood Pressure in Postpartum Women
A NA study of Hypertension, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 1,607
- Enrollment target
- 1
- Study location
NCT05236725: Completed NA study of Hypertension, sponsored by Wake Forest University Health Sciences.
NCT05236725 is a NA study of Hypertension that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 1,607 participants, below the 3,504-participant average among 470 other Hypertension trials with a reported enrollment target (54% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05236725, a NA study of Hypertension, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,607 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research study is to find out the usefulness of checking a woman's blood pressure remotely (at home) for 3 weeks after being discharged from the hospital after having a baby (or babies). Some women can develop hypertension, or high blood pressure, after delivery even if they have not had this problem before or during their pregnancy. Untreated or unknown high blood pressure can lead to medical complications, and if severe, can be life threatening. Monitoring, or checking, remote blood pressure after a woman has delivered her baby (or babies) has been suggested to be a better way to monitor blood pressures without having to stay in the hospital for a longer time after delivery. Other researchers report that women who have checked their blood pressure remotely after delivery found out that this was both possible and acceptable.
Primary Outcome
Used to determine feasibility of remote blood pressure monitoring intervention (rBPM) in postpartum women. This measure represents the median number of remote blood pressure monitoring (rBPM) measurements collected per participant during the study period. The total number of rBPM readings obtained for each participant was calculated, and the median value across all participants in the analysis population was reported
Conditions Studied
Interventions
- BEHAVIORAL Instructions
- DEVICE Remote Blood Pressure Cuff
- DEVICE Blood pressure monitoring smart phone app, BabyScripts™
Study Locations (1)
North Carolina
- Atrium Health Wake Forest Baptist - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,607 participants |
| Start Date | 2022-03-01 |
| Est. Completion | 2025-11-12 |
| Phase | NA |
What the finished NCT05236725 record still lists
NCT05236725 is an interventional study that assigns participants to a tested intervention. Its 1,607 participants enrollment target places it among the larger protocols in the corpus, below the 3,504-participant average among 470 other Hypertension trials with a reported enrollment target (54% lower).
The record links to 1 condition, with Hypertension appearing as the primary indexed condition, and to 3 interventions - of which Instructions is the first listed.
NCT05236725 reports a single indexed study location in North Carolina.
Frequently Asked Questions
What is clinical trial NCT05236725 about?
NCT05236725 is a clinical study titled "Monitoring and Testing of Blood Pressure in Postpartum Women". The purpose of this research study is to find out the usefulness of checking a woman's blood pressure remotely (at home) for 3 weeks after being discharged from the hospital after having a baby (or babies). Some women can develop hypertension, or high blood pressure, after delivery even if they have...
What is the current status of trial NCT05236725?
This trial is currently completed. It is a NA study. The enrollment target is 1,607 participants. The study started on 2022-03-01. Estimated completion is 2025-11-12.
What conditions does trial NCT05236725 study?
This clinical trial studies the following conditions: Hypertension.
What interventions are being tested in trial NCT05236725?
The interventions under investigation include: Instructions (BEHAVIORAL), Remote Blood Pressure Cuff (DEVICE), Blood pressure monitoring smart phone app, BabyScripts™ (DEVICE).
Who is sponsoring clinical trial NCT05236725?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05236725 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT05236725's enrollment target sits among peer trials
1,607 43rd of 470 higher than 428 of 470 other Hypertension trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Hypertension trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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