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NCT06019715Completed

Remote Postpartum Intervention Targeting Movement Behaviors After Hypertensive Disorders of Pregnancy

Source: ClinicalTrials.gov · Last updated 10 May 2024

Brief summary (registry, in English)

The purpose of this study is to test the feasibility, acceptability, and preliminary efficacy of a postpartum physical activity intervention after a pregnancy complicated by a Hypertensive Disorder of Pregnancy. The study will also assess the effects of the remote postpartum intervention on blood pressure. To do this, we will recruit individuals that are 3-6 months postpartum a pregnancy complicated by a hypertensive disorder to participate in a 4-month health coaching intervention aimed to promote physical activity and was informed by formative work done previously.

Status (registry)
Completed
Study type
Interventional
Enrollment
20 (actual)
First submitted
24 Aug 2023
Start date
1 Jun 2023
Primary completion date
1 Mar 2024
Lead sponsor
Jackie Dziewior
NCT number
NCT06019715

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From 1 Jun 2023 to the primary completion date, 1 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior bariatric surgery
  • Currently takes medication to reduce weight or anti-hypertensives

Other illness

  • Diagnosed with diabetes, kidney disease, cardiovascular disease

Other

  • Current enrollment in another physical activity or sedentary behavior intervention study
  • Recommend to limit physical activity by a healthcare provider

Who the study is looking for

  • \<6 months postpartum from a pregnancy complicated by a hypertensive disorder
  • Have self-reported insufficient activity (\<150 minutes of moderate to vigorous physical activity per week)
  • Own a smartphone

Age in the registry: 18 years to 45 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Iowa
Coordinator of this site? Confirm its status
Iowa CityUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.