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RecruitingNCT07356518Updated Apr 27, 2026

Telehealth and Remote Blood Pressure

An interventional study of Telehealth visits and In-person visits in Hypertension and Hypertension in Pregnancy, sponsored by Wake Forest University Health Sciences. Recruiting at 1 site in United States. Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-04-27.

Sponsored by Wake Forest University Health Sciences · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Apr 2026; still recruiting 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

The purpose of this research study is to compare the management of chronic hypertension during pregnancy using telehealth visits with blood pressure telemonitoring and health coaching as compared to standard in person clinic visits. The study involves pregnant woman aged 18-45 who are receiving care for chronic hypertension. Participation in this research study will last until their baby is delivered. The number of in-person clinic visits depends on the participant's treatment assignment. Those assigned to telehealth visits will have telehealth visits alternating with clinic visits every two weeks until the end of pregnancy week 31. Those assigned to telehealth visits will also have five sessions with a health coach via telephone or video from the time of enrollment until the end of pregnancy week 36.

Read the detailed description

Hypertension (HTN) in pregnancy requires weekly or bi-weekly in-person visits. Telehealth visits with remote blood pressure (BP) telemonitoring may be an alternative to frequent in-person visits improve adherence. However, the feasibility of this approach in pregnancy is lacking and studies are limited on the use of remote BP telemonitoring in chronic HTN (cHTN) during pregnancy. A digital health platform for BP management in pregnant women at risk for preeclampsia (women with cHTN, prior preeclampsia or kidney disease) found fewer admissions for HTN or suspected preeclampsia in the intervention compared to usual care. There is a critical need to investigate the feasibility (willingness and adherence), and safety of this intervention. Without ascertaining the feasibility of telehealth and remote BP monitoring, it remains a challenge to tackle the no-show rates and suboptimal medication adherence during pregnancy.

Objectives Aim 1: To determine the feasibility of incorporating telehealth clinic visits with remote BP telemonitoring alternating with in-person clinic visits in the management of cHTN in pregnancy in the clinic by evaluating willingness to enroll, completion rate and adherence versus standard care (in-person clinic visits alone). This working hypothesis is that this approach will be as feasible as standard care.

Aim 2: To explore safety outcomes of telehealth clinic visits combined with blood pressure remote telemonitoring alternating with in-person clinic visits in the management of chronic hypertension in pregnant patients in the clinic by measuring the incidence of hypotension, syncope or hospitalization/emergency room visits for severe HTN compared to standard care. The working hypothesis is that this approach will be comparable in safety to standard care.

02

Conditions studied

  • Hypertension
  • Hypertension in Pregnancy

Keywords

  • high blood pressure
  • pre-eclampsia
  • hypertension during pregnancy
03

In context

Hypertension

6,689 studies on the registry are indexed under Hypertension; 965 are open to participants now.

This study's planned enrollment of 60 is below the median of 90 across 4,995 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Wake Forest University Health Sciences is the lead sponsor of 1,320 studies on the registry; 199 are open to participants now.

Of its 323 completed or terminated interventional studies of FDA-regulated products, 243 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • prior diagnosis of Chronic hypertension (cHTN)
  • Pregnant women
  • Known: documented diagnosis or on antihypertensive medication prior to pregnancy

Exclusion criteria

Exclusion Criteria:

  • Any significant chronic medical or psychiatric illness that, in the investigator's opinion, would prevent participation in the study
  • Cardiac disorders: cardiomyopathy, angina, Coronary Artery Disease (CAD)
  • Current substance abuse disorder
  • Multifetal pregnancy
  • Participation in another study without prior approval
  • Plan to deliver outside Atrium Health Wake Forest Baptist
  • Prior stroke
  • Severe hypertension
  • Suspected or known fetal major structural/chromosomal abnormality or fetal demise
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Telehealth Cycle

    Participants in this arm will be provided telehealth visits in addition to the blood pressure telemonitoring.

    Behavioral: Telehealth visits · Behavioral: In-person visits

  • Active comparator
    Standard of Care

    In person clinic visits

    Behavioral: In-person visits

Interventions

  • BehavioralTelehealth visits

    remote visits with participants

  • BehavioralIn-person visits

    standard of care visits with care provider in person

06

What researchers measure

Primary outcomes

  1. Feasibility of telehealth with remote BP telemonitoring compared to standard care

    willingness to enroll (number of patients enrolled divided by number of patients reached), study completion rate, adherence compared to standard care). Adherence will be defined as taking medication at least ≥80% of the time, recording ≥70% of weekly BP readings in the intervention group only and completing ≥70% of antenatal telehealth/clinic visits.

    Time frame: Gestational Week 31

  2. Safety of telehealth combined with telemonitoring compared to standard care

    The number of adverse events reported (hypotension, syncope or hospitalization/emergency room visit for severe HTN

    Time frame: Gestational Week 31

Secondary outcomes

  1. Patient satisfaction Scores

    at the end of 31 weeks, each participant will complete a patient research satisfaction survey - Strongly disagree 0, disagree 1, neither agree nor disagree 2, agree 3, strongly agree 4

    Time frame: Gestational Week 31

  2. Clinical team member (Medical Assistant, Nursing staff, Medical Provider, Scheduler) satisfaction Scores

    at the end of 31 weeks, each provider of record for each participant will be invited to complete a research satisfaction survey. Nurses, medical assistants, schedulers at the Comprehensive Fetal Care Center who have participated in the telehealth visit with remote monitoring will be invited to complete a research satisfaction survey - Strongly disagree 0, disagree 1, neither agree nor disagree 2, agree 3, strongly agree 4

    Time frame: Gestational Week 31

07

Study locations

1 of 1 sites recruiting
  • Wake Forest University Health Sciences
    Winston-Salem, North Carolina 27157, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Individual participant data that underline the results reported in this article, after de-identification (text, tables and appendices)

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07356518
Lead sponsor
Wake Forest University Health Sciences
Responsible party
Sponsor
First posted
Jan 21, 2026
Start date
Apr 22, 2026
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Apr 27, 2026

Study contacts

Ejiro Obioma, MBBS MMCi
Contact
Ejiro.Obioma@Advocatehealth.org
704-355-2000
Aderonke Adeniyi, MD, MS
Contact
aderonke.adeniyi@advocatehealth.org
337 713 2278
Aderonke O Adeniyi, MD, MS
principal investigator · Wake Forest University Health Sciences

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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