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REmote Physical ACtivity Intervention for High Blood Pressure Postpartum

REACH BP: REmote Physical ACtivity Intervention for High Blood Pressure Postpartum

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07127731
Acronym
REACH BP
Enrollment
60
Registered
2025-08-17
Start date
2027-04-01
Completion date
2028-04-01
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension (HTN), Hypertension ,Pregnancy, Physical Activity

Keywords

hypertension, pregnancy, postpartum, physical activity

Brief summary

The purpose of this intervention is to help new mothers who had elevated blood pressure during pregnancy become more physically active after birth. The investigators will connect data from FitBits to the electronic health record. Women will then get weekly messages with feedback and goals to help them stay active. The investigators will test if the intervention improves step counts and blood pressure after pregnancy. The investigators will also test if the intervention is feasible and enjoyed by postpartum women.

Interventions

BEHAVIORALPatient Portal Messaging

Participants will receive weekly messages via their patient portal including feedback on their step counts and step count goals based on data from their FitBits

BEHAVIORALFitBit EHR Linkage

Participants will receive FitBits and link this step count data with the Electronic Health Record (EHR)

Sponsors

Northwestern University
Lead SponsorOTHER
National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Delivery of a live birth at Northwestern Medicine 6-12 weeks prior * Systolic blood pressure 120-139 or diastolic blood pressure 80-89 during the first 20 weeks of gestation * Low self-reported physical activity levels * Able to access the internet at least weekly * Have patient portal account or willing to set one up * Willing to wear a FitBit * Spoken and written English or Spanish language fluency

Exclusion criteria

* Medical contraindications to participating in a structured physical activity program * Currently participating in a structured physical activity or weight loss program * Hypertensive disorder of pregnancy (e.g., preeclampsia, gestational hypertension, eclampsia)

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of RecruitmentFrom enrollment to the end of the 24 week interventionNumber of participants enrolled in the intervention
Feasibility of Participant RetentionAt study weeks 12 and 24Percent of enrolled participants who continue to participate in the intervention
Feasibility of FitBit+EHR linkageFrom enrollment to the end of the 24 week interventionPercent of intervention days FitBit data are linked to the Electronic Health Record
Feasibility of Intervention MessagingFrom enrollment to the end of the 24 week interventionPercent of weekly messages that are read by participants
Acceptability of the InterventionStudy week 24Participants will fill out a survey to assess the extent to which they were satisfied with individual intervention components including FitBit usage, portal messaging, blood pressure and weight assessments, surveys, intervention length and intervention delivery. Each component will be rated on a 5-point Likert Scale in which 1 represents very dissatisfied (lowest score) and 5 represents very satisfied (highest score).

Contacts

CONTACTNatalie A Cameron, MD, MPH
natalie.cameron@northwestern.edu312-503-2137

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026